CA2079813A1 - Method of treatment with hsp70 - Google Patents
Method of treatment with hsp70Info
- Publication number
- CA2079813A1 CA2079813A1 CA002079813A CA2079813A CA2079813A1 CA 2079813 A1 CA2079813 A1 CA 2079813A1 CA 002079813 A CA002079813 A CA 002079813A CA 2079813 A CA2079813 A CA 2079813A CA 2079813 A1 CA2079813 A1 CA 2079813A1
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- hsp70
- cell
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- cells
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- General Chemical & Material Sciences (AREA)
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- Gastroenterology & Hepatology (AREA)
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- Proteomics, Peptides & Aminoacids (AREA)
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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Abstract
A method of combating mortality in a cell or tissue under stress is disclosed. The method comprises contacting hsp70 to the cell or tissue in an amount effective to enhance the survival of that cell or tissue. The method may be employed in the combating of atherosclerosis, restenosis after angioplasty, and nerve damage in human or animal subjects in need of such treatment. A
pharmaceutical composition comprising a therapeutically effective amount of hsp70 in a pharmaceutically acceptable formulation is also disclosed.
pharmaceutical composition comprising a therapeutically effective amount of hsp70 in a pharmaceutically acceptable formulation is also disclosed.
Description
~ . ~
~ . .
METHOD OF TREATMENr WITH HSP70 -Field of the Invention The present invention relates to methods of enhancing the survivability of cells and tissues by treating the same with exogenous hsp70.
Back~round o~ the !nvenbon Heat shock proteins ~hsps) are highly conserved constitutive and induced proteins found in cells from bacteria to human beings. S. Lindquist, Ann. Rev.
Biochem 55, 1151 (1986). The constitutive hsps are critical to many diverse cellular functions. The most ubiquitous and best studied hsp family, the group of hsp's with molecular weights close to 70,000 claltons (hsp70), has been shown to assist in translocation of proteins into the endoplasmic reticulum and mitochondria, R. Deshais et al., Nature 332, 800 tl988), W. Chirico et al., Nature 332, 805 ~1988). Hsp 70 also has been implicated as the clathrin-uncoating ATPase, T. Chapell et al., Cell 45, 3~ (1986). Potential structural functions of other hsps include: linking the actin cytoskeleton to the plasmale~ma, S. Koyasu et al., Proc.
Natl. Acad. Sci. USA 83, 8054 (1986); specifically binding saturated fatty acids, P. Guidon and L.
Hightower, Biochemistry 25, 3231 (1986) P. Guidon and L.
Hightower, J. Cell Physi~l. 128, 239 (1986), and as ,. . , . . , .. ,: ..
~ ~ 207981 3 . 'G 2 components of some steroid binding receptors. E. Baulieu and M. Catelli, Alan R. Liss. Inc.,_New York, 275 (1989).
These proteins also appear to act as antigens in anti-bacterial, D. Young et al., Proc. Natl Acad. Sci. USA
85, 4267 (1988); A. Mehlert et al., Biochem. Soc. Trans.
16, 721 (1988), and autoimmune reactions. S. Minota et al., J. Exp. Med. 168, 1475 (1988), S. Minota et al., J.
Clin. Invest. 81, 106 (1988). Several other functions ; have been suggested as well. See S. Lindquist, Ann. Rev.
Biochem 55, 1151 (1986), M. Schlesinger et al., Cold Spring Harbor Laboratory, 1982, M. Pardue et al., Alan R.
Liss, Inc. (1989~, M. Schlesinger, J. Cell Biol. 103, 321 (1986), E. Craig, CRC_Critical Revlews in Biochemistry, ~- Vol. 18._no. 3, 239 (1985).
; 15 The inducible ~orms of hsps are elicited by a variety of stressors, including elevated temperature, M.
Schlesinger et al., Cold Spring Harbor Laboratory, 1982, heavy metals, M. Schlesinger et al., Alan R. Liss Inc.
137 (1989), amino acid analogs, P. Kelley and M.
Schlesinger, ~11 15, 1277 (1978), L. Hightower, J. Cell.
Physiol. 102, 407 (1980), oxidative radicals, M.
Ashburner, Chromosoma 31, 356 (1970), J. Compton and B.
McCarthy, Cell 14, 191 (1978) ischemia or return from anoxia, S. Guttman, Cell 22, 299 (1980), M. Ashburner and J. Bonner, Cell 17, 241 (1979), mechanical trauma, L.
Hightower and F. White, Cold Spring Harbor Laboratory, 369 (1982), D. Gower et al., J. Cell Biol. 103, 291 (1986), and abnormal proteins. J. Ananthan et al., Science 232, 522- (1986). The unifying functional characteristic is that they act to maintain normal cellular function under non-ideal conditions.
The functional importance of hsps to cells under stress extends to the arterial wall and atherosclerosis. The developing plaque involves 3S histological and biochemical changes in the composition of the arterial wall, R. Ross, N. Enq. Jt Med. 314, 488 (1986). In chronically ~tressed atherosclerot:ic plaque ", ' ~: " ' ~ . ' `"
~ .
' 20798~
: 3 cells, hsp alterations~may ~ave serious implications. As ~`an example, one general effect of hsps is to stabilize membranes of cells, R. Shiver et al., Eur~ J. Cell ~iol.
46, 181 (1988), and it has been suggested that stabiliz~tion of arterial lysosomal membranes may facilitate plaque cells to entrap lipids, J. Berthet et al., Biochem. J. 50, 182 (1951), C. deDuve, Harvey Lectures 59, 49 tl965), P. Berberian et al~, Fed. Proc.
43, 711 (1984). Cell stabilization by hsps additionally may help to determine the relative survival of cells within various regions of the developing plaque, while its relative deficiency may define areas vulnerable to necrosis.
There is evidence that hsps can be exchanged between cells. L. Hightower and P. Guidon, J. ~ell.
Physiol. 138, 257 (1989), M. Tytell et al., Brain Res.
363, 161 (1986). Thus, it is possible that hsps' effects may not be limited to the stressed cell synthesizing them. However, no one has tested the effect of exogenously added hsps on cell survival. The present invention is based on our findings after undertaking such tests.
Summar~ of ~e Inven~on A first aspect of the present invention is a method of combating mortality in a cell under stress.
The method comprises contacting hsp70 to_the cell in an amount effective to enhance the survival of that cell.
A second aspect o~ the present invention is a method of combating mortality in a tissue under stress, such as arterial tissue. The method comprises contacting hsp70 to the tissue in an amount effective to enhance the survival of cells residing in that tissue. The tissue may be treated in vivo or in vit~o. Among other things, this method is useful for preserving organs for transplant.
A third aspect of the present invention is a metho~ of combatinç atherosclerosis-in a human or animal :: -. . : . : .: . - .
., . : : ~. .: .
.
..
~ . .
METHOD OF TREATMENr WITH HSP70 -Field of the Invention The present invention relates to methods of enhancing the survivability of cells and tissues by treating the same with exogenous hsp70.
Back~round o~ the !nvenbon Heat shock proteins ~hsps) are highly conserved constitutive and induced proteins found in cells from bacteria to human beings. S. Lindquist, Ann. Rev.
Biochem 55, 1151 (1986). The constitutive hsps are critical to many diverse cellular functions. The most ubiquitous and best studied hsp family, the group of hsp's with molecular weights close to 70,000 claltons (hsp70), has been shown to assist in translocation of proteins into the endoplasmic reticulum and mitochondria, R. Deshais et al., Nature 332, 800 tl988), W. Chirico et al., Nature 332, 805 ~1988). Hsp 70 also has been implicated as the clathrin-uncoating ATPase, T. Chapell et al., Cell 45, 3~ (1986). Potential structural functions of other hsps include: linking the actin cytoskeleton to the plasmale~ma, S. Koyasu et al., Proc.
Natl. Acad. Sci. USA 83, 8054 (1986); specifically binding saturated fatty acids, P. Guidon and L.
Hightower, Biochemistry 25, 3231 (1986) P. Guidon and L.
Hightower, J. Cell Physi~l. 128, 239 (1986), and as ,. . , . . , .. ,: ..
~ ~ 207981 3 . 'G 2 components of some steroid binding receptors. E. Baulieu and M. Catelli, Alan R. Liss. Inc.,_New York, 275 (1989).
These proteins also appear to act as antigens in anti-bacterial, D. Young et al., Proc. Natl Acad. Sci. USA
85, 4267 (1988); A. Mehlert et al., Biochem. Soc. Trans.
16, 721 (1988), and autoimmune reactions. S. Minota et al., J. Exp. Med. 168, 1475 (1988), S. Minota et al., J.
Clin. Invest. 81, 106 (1988). Several other functions ; have been suggested as well. See S. Lindquist, Ann. Rev.
Biochem 55, 1151 (1986), M. Schlesinger et al., Cold Spring Harbor Laboratory, 1982, M. Pardue et al., Alan R.
Liss, Inc. (1989~, M. Schlesinger, J. Cell Biol. 103, 321 (1986), E. Craig, CRC_Critical Revlews in Biochemistry, ~- Vol. 18._no. 3, 239 (1985).
; 15 The inducible ~orms of hsps are elicited by a variety of stressors, including elevated temperature, M.
Schlesinger et al., Cold Spring Harbor Laboratory, 1982, heavy metals, M. Schlesinger et al., Alan R. Liss Inc.
137 (1989), amino acid analogs, P. Kelley and M.
Schlesinger, ~11 15, 1277 (1978), L. Hightower, J. Cell.
Physiol. 102, 407 (1980), oxidative radicals, M.
Ashburner, Chromosoma 31, 356 (1970), J. Compton and B.
McCarthy, Cell 14, 191 (1978) ischemia or return from anoxia, S. Guttman, Cell 22, 299 (1980), M. Ashburner and J. Bonner, Cell 17, 241 (1979), mechanical trauma, L.
Hightower and F. White, Cold Spring Harbor Laboratory, 369 (1982), D. Gower et al., J. Cell Biol. 103, 291 (1986), and abnormal proteins. J. Ananthan et al., Science 232, 522- (1986). The unifying functional characteristic is that they act to maintain normal cellular function under non-ideal conditions.
The functional importance of hsps to cells under stress extends to the arterial wall and atherosclerosis. The developing plaque involves 3S histological and biochemical changes in the composition of the arterial wall, R. Ross, N. Enq. Jt Med. 314, 488 (1986). In chronically ~tressed atherosclerot:ic plaque ", ' ~: " ' ~ . ' `"
~ .
' 20798~
: 3 cells, hsp alterations~may ~ave serious implications. As ~`an example, one general effect of hsps is to stabilize membranes of cells, R. Shiver et al., Eur~ J. Cell ~iol.
46, 181 (1988), and it has been suggested that stabiliz~tion of arterial lysosomal membranes may facilitate plaque cells to entrap lipids, J. Berthet et al., Biochem. J. 50, 182 (1951), C. deDuve, Harvey Lectures 59, 49 tl965), P. Berberian et al~, Fed. Proc.
43, 711 (1984). Cell stabilization by hsps additionally may help to determine the relative survival of cells within various regions of the developing plaque, while its relative deficiency may define areas vulnerable to necrosis.
There is evidence that hsps can be exchanged between cells. L. Hightower and P. Guidon, J. ~ell.
Physiol. 138, 257 (1989), M. Tytell et al., Brain Res.
363, 161 (1986). Thus, it is possible that hsps' effects may not be limited to the stressed cell synthesizing them. However, no one has tested the effect of exogenously added hsps on cell survival. The present invention is based on our findings after undertaking such tests.
Summar~ of ~e Inven~on A first aspect of the present invention is a method of combating mortality in a cell under stress.
The method comprises contacting hsp70 to_the cell in an amount effective to enhance the survival of that cell.
A second aspect o~ the present invention is a method of combating mortality in a tissue under stress, such as arterial tissue. The method comprises contacting hsp70 to the tissue in an amount effective to enhance the survival of cells residing in that tissue. The tissue may be treated in vivo or in vit~o. Among other things, this method is useful for preserving organs for transplant.
A third aspect of the present invention is a metho~ of combatinç atherosclerosis-in a human or animal :: -. . : . : .: . - .
., . : : ~. .: .
.
..
2~98~
subject in need of s`lch ~reatment. The method comprises administering the subject hsp70 in an amount effective to reduce necrosis in arterial plaques residing in the subject.
A fourth aspect of the present invention is a method of combating arterial restenosis after angioplasty in a human or animal subject in need of such treatment comprising administering arterial tissue resicling in the subject in need of such treatment hsp70 in a restenosis-combating amount.
A fifth aspect of the present invention is a method of combating nerve damage in a human or animal subject in need of such treatment, comprising administering the subject hsp70 in an amount effective to enhance the survival of nerve cells under stress.
A sixth aspect of the present invention is a pharmaceutical composition comprising a therapeutically effective amount of hsp70 in a pharmaceutically acceptable formulation.
A seventh aspect of the present invention is the use of hsp70 for the preparation of a pharmaceutical formulation for the combating of mortality in arterial tissue.
An eighth aspect of the present invention is the use of hsp70 for the preparation of a pharmaceutical formulation for the combating of mortality in nerve tissue.
Brief DescnPbon of the Drawinqs Figure 1 illustrates the structure-linked latency of lysosomal enzymes versus viability for r isolated cells without added hsp70. Data represent pooled normal (open square) and diseased (closed square) monkey aortic cell values (n - 23 across all temperatures tested (r = 0.85).
Figure 2 illustrates the effect of temp~rature on arterial cell viability (~a) and structure-linked lysc~omal latenc~ (2b) without ad~ed hsp70. Means of 6 o 2079~13 , ~ ;
aortas ~/-s.e.m. are shown. ~;guré~2a illustrates that a significant (p < 0.0005) decline in viability occurs with increased temperature of incubation; figure 2b illustrates that a significant (p ~ 0.004) decline in lysosomal latency occurs with increased temperature of i incubation.
Figure 3 illustrates the close-dependent effect of hsp70 on viability (including time zero and with no ; added hsp70). Means of 4 aortas ~/- S.E.M. are shown.
lo A significant difference in viability occurs at a dose of 10 ng/103 cells (p < 0.05~, with no significant increase observed with a ten-fold higher dose.
Figure 4 illustrates the temperature-dependent effect of hsp70 on arterial cell viability. Each ; 15 temperature was tested with and without 10 ng hsp70 per 103 cells. Means o~ 6 samples of cells from aortas +/-s.e.m. are shown. Comparison between all treated versus untreated samples showed a significant (p ~ 0.05) increase in viability with added hsp at 37C.
Figure 5 illustrates the temperature-dependent effect of hsp70 on structure-linked latency of lysosomal enzymes. Means of 6 aorta samples +/- s.e.m. are shownO
No significant increase occurred with exogenous hsp.
Figure 6 illustrates the effect of intravitreal injection of hsp70 in the right eye on retinal sensitivity to light damage. The right-left differences in photoreceptor area (square ~m) are shown. Significant prevention of photoreceptor destruction occured at the high dose of hsp70.
subject in need of s`lch ~reatment. The method comprises administering the subject hsp70 in an amount effective to reduce necrosis in arterial plaques residing in the subject.
A fourth aspect of the present invention is a method of combating arterial restenosis after angioplasty in a human or animal subject in need of such treatment comprising administering arterial tissue resicling in the subject in need of such treatment hsp70 in a restenosis-combating amount.
A fifth aspect of the present invention is a method of combating nerve damage in a human or animal subject in need of such treatment, comprising administering the subject hsp70 in an amount effective to enhance the survival of nerve cells under stress.
A sixth aspect of the present invention is a pharmaceutical composition comprising a therapeutically effective amount of hsp70 in a pharmaceutically acceptable formulation.
A seventh aspect of the present invention is the use of hsp70 for the preparation of a pharmaceutical formulation for the combating of mortality in arterial tissue.
An eighth aspect of the present invention is the use of hsp70 for the preparation of a pharmaceutical formulation for the combating of mortality in nerve tissue.
Brief DescnPbon of the Drawinqs Figure 1 illustrates the structure-linked latency of lysosomal enzymes versus viability for r isolated cells without added hsp70. Data represent pooled normal (open square) and diseased (closed square) monkey aortic cell values (n - 23 across all temperatures tested (r = 0.85).
Figure 2 illustrates the effect of temp~rature on arterial cell viability (~a) and structure-linked lysc~omal latenc~ (2b) without ad~ed hsp70. Means of 6 o 2079~13 , ~ ;
aortas ~/-s.e.m. are shown. ~;guré~2a illustrates that a significant (p < 0.0005) decline in viability occurs with increased temperature of incubation; figure 2b illustrates that a significant (p ~ 0.004) decline in lysosomal latency occurs with increased temperature of i incubation.
Figure 3 illustrates the close-dependent effect of hsp70 on viability (including time zero and with no ; added hsp70). Means of 4 aortas ~/- S.E.M. are shown.
lo A significant difference in viability occurs at a dose of 10 ng/103 cells (p < 0.05~, with no significant increase observed with a ten-fold higher dose.
Figure 4 illustrates the temperature-dependent effect of hsp70 on arterial cell viability. Each ; 15 temperature was tested with and without 10 ng hsp70 per 103 cells. Means o~ 6 samples of cells from aortas +/-s.e.m. are shown. Comparison between all treated versus untreated samples showed a significant (p ~ 0.05) increase in viability with added hsp at 37C.
Figure 5 illustrates the temperature-dependent effect of hsp70 on structure-linked latency of lysosomal enzymes. Means of 6 aorta samples +/- s.e.m. are shownO
No significant increase occurred with exogenous hsp.
Figure 6 illustrates the effect of intravitreal injection of hsp70 in the right eye on retinal sensitivity to light damage. The right-left differences in photoreceptor area (square ~m) are shown. Significant prevention of photoreceptor destruction occured at the high dose of hsp70.
3 0 C~tailed DescriPtion ~ the Invent~on Cells of any origin may be treated by the method of the present invention, including animal, plant, and bacterial cells. Cells may be treated in vitro or ln vivo. Likewise, tissues of any origin, including animal and plant tissue, may be trea~ed by the method of the present invention either in vitro or in vivo. Animal cells and tiss-es are pref~rred for carrying out the .
.
, ~ ', . " : ' ~
- : ', '- :,, , , ' o 2079813 ,,; ~ ,. -p~esent invention, with ma~nall~n (e.g., dog, cat, human) cells and tissue particularly pre~erxed. The term "animal" as used herein, refers to the subjects of ~ veterinary medicine, such as dog, cat, cow, pig~ and horse.
~ Cells and tissue which are under stress are treated with hsp70 to combat mortality. For examplel cells which are maintained in culture (e.g., for the purpose of producing proteins or other materials from the cells) or tissue which is maintained in culture (e.g.0 complete organs such as heart, lung, liver or kidney prior to transplant) may be considered as "under stress"
for the purpose of practicing the present invention. For example, organs could be immersed in a solution containing HSP70, or a larger organ perfused through its vasculature, with an HSP70 solution. The HSP70 would be taken up by the cells of the organ, making them more resistant to the lack of blood, nutrients and other needed substances that exists once they are removed from the body. Likewise, the ~SP70 could be included in a reperfusion solution to combat tissue reperfusion injury.
The HSP70 may be added to known solutions and used in accordance with procedures known to those skilled in the art for these purposes. Such solutions and procedures are disclosed in U.S. Patent No. ~,920,044, titled "Intracellular Flush Solution for Preserving Organs", U~S. Patent No. 4,879,283 titled "Solutions ~or the Preservation of Organs", U.S. Patent No. 4,873,230 titled "Composition for the Preservation of Organs", and U.S.
Patent No. 4,798,824 titled "Perfusate for the Preservation of Organs". Applicants intend the disclosures of these and all other patents cited herein to be incorporated herein by reference.
Tissue under stress ln vivo may also be treated. For example, arterial and myocardial tissue may be treated by adminis~ering hsp70 during by-pass surgery to enhance the survivahility o~ cells ~n that tissue.
-. .
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Cardiac ischemi~ may ~e t:reated by a~min~stering hsp70 about the time of myocardial infarction to enhance the survivability of cells in those tissues. The kidney may be protected from damage from toxic substances such as the antibiotic Gentamicin by the administration of hsp700 :f!
Arterial tissue may be administered hsp70 during laser angioplasty and atherectomy to reduce damage to these tissues arising from such procedures.
Nerve tissue (i.e., peripheral nerve and central nerve) which is under stress in vivo may also be treated by the method of the present invention. For example, peripheral nerves which are severed are subject to retrograde degeneration, which degeneration may culminate in death of the nerve cell, or soma, if too great a portion of the nerve's axon is distal to the site of the cut. If degeneration does not culminate in cell death, then an opportunity exists for the nerve to regenerate. Thus, hsp70 may be administered to such nerve tissue, through administration to the host animal, to combat cell mortality which may result from the severing of the peripheral nerve.
Nerve tissue may also be subject to anoxic stress in vivo. For example, anoxic stress may arise -from a stroke or burst aneurism which damages nerve tissue by depriving the tissue of blood. When central nerve tissue is so damaged, the damage typically occurs in a watershed pattern in relation to the blood vessels:
tissue closest the damaged supply vessel is most severely damaged; tissue furthest from the damaged vessel which is supplied by other vessels is least severely damaged;
tissue intermediate of these extremes shows intermediate damage. Afflicted subjects are administered hsp70 to combat mortality in cells subject to this type of stress.
As noted above, the present invention may be employed to combat restenosis a~ter angioplasty.
Angioplasty is a procedure for dilating arteries which are occluded or blo~ked. In a typical transluminal ~ ' . ~ ' , : -2079~13 -"` ' "`" --E}--baloon angioplast~ procedure, a cath~ter ~hich carries an inflatable dilation balloon at the clistal end is employed to reshape a partially occluded arl-ery. The balloon is inserted in the deflated condition in the restricted portion of the artery and inflated so that the occluded lumen is reshaped by the dilation balloon to allow better passage o~ blood. The obstructing material is neither - dislocated nor removed from the vessel, but rather pressed against the wall. The wall, in turn, is stretched to accommodate the previously obstructing material. After the lumen has been reshaped, the dilation balloon is deflated and removed. The site of the formed obstruction may, however, become reoccluded when/if the vessel returns to its previous configuration:
a phenom~non known as "restenosis." A variety of angioplasty procedures and instruments are known. See e.q. U.S. Patent Nos. 4,838, 269 and 4,794,928 (the disclosures of which are to be incorporated herein by reference). A subject in need of treatment to prevent restenosis (i.e., either during angioplasty or after angioplasty prior to the onset of restenosis) may be treated by administering hsp70 to the lumen of the vessel which has been reshaped (e.g., by intraveneous injection or intraarterial injectionl. Any administration which places hsp70 into the bloodstream of the subject or at the site of treatment is suitable, but preferably the administration procedure will direct the hsp70 to the particular site of the angioplasty (i.e., the vessel wall which has been reshaped). For example, the hsp70 may be applied directly to the site of treatment by means of a sweating baloon catheter (i~e., an angioplasty balloon which is perforated so as to administer hsp70 through the perforations ~o the arterial cell wall during angioplasty).
Skin tissue under stress due to wounds, burns, ulcers, in~ections, and other types o~ traumatic injury may be treated by ~e me~hod o~ the present invsntion.
~l 2079~13 ~t ~
~ , _g _ For such purposes HSP70 may be administerea ~by~ ~opical application to the skin in the form o~ a salve o~ cream to enhance repair and healing of the tissue. Tissues may also be under stess due to chemotherapeutic treatment, as in cancer chemotherapy. In such cases HSP70 may be administered subsequent to the chemotherapeutic treatment as a "rescue" agent.
Hsp70 is a member of the hleat shock protein (or "hsp") family, which are produced when cells or organisms are exposed to elevated temperatures. This response has been observed in essentially all organisms to date. See ~enerally S. Lindquist, The Heat-Shock Response, Ann.
Rev. Biochem. 55, 1151 (1986). For example, hsp70 has been found in plants. See, e.q.. J. Marshall et al., ~roc. Natl. Acad. Sci. USA 87, 374 (1990). The hsp70 ~roup is the most highly conserved member o~ the hsp family. For example, the human protein is 73% identical to the Drosophila protein and is 50% identical to the corresponding Escherichia coli protein dnaK. See B.
Bukau et al., DnaK and GroE Proteins Play Roles in E.
coli Metabolism at Low and Intermediate Temperatures as Well as at High Temperatures, in Stress-Induced Proteins, 27 (1989)(published by Alan R. Liss, Inc.). Many of the di~ferences are merely homologous substitutions, and there are regions of homology which those in the ~ield consider to be extraordinary. S. Lindq~ist, supra at 1155-56.
Within some species, the term "hsp70" itself denotes a ~amily of closely related protein~, all found in that species. In Saccharomyces cerevisiae, strains bearing certain hsp70 mutations are nonviable, but viability can be restored by altering the transcriptional regulation o~ the remaining genes. See E. Craig st al., Complex Regulation of Three Heat Inducible hsp70 Related Genes in S~ccharomyces cerevisiae, in Stress-Induced Proteins, 51 ~1989). In view of the biological interchangeability and hsmolo~y, any membe~ of the hsp70 . ~ ' ' `' . . '' , . ' : . - . :' ' : .
2~79gl3 ': ` i ! ~
family within a species is contemplate~ as useful in practicing the p~esent invention.
As to species of origin, in view o~ the highly conserved nature of the hsp70 family among broadly divergent species, hsp70 from any species of origin is contemplated as useful in praclicing the present invention tnumerous references to hsp70 are set forth above, the disclosures of which are ~o be incorporated herein by reference). Thus, animal, plant ~e.g., Pisum sativum), and bacterial hsp70 are all contemplated as useful for treating cells or tissue of any origin in practicing the present invention. It is, nevertheless, contemplated that an hsp70 of related origin to the cell or tissue being treated will be preferred for practicing the present invention. For example, plant hsp70 is contemplated as preferred for treating plant cells or tissue, animal hsp70 is contemplated as preferred for treating animal cells or tissue, mammalian hsp70 is contemplated as preferred for treating mammalian cells or tissue, and so on.
The term 'IHSP 70" is intended to include active fragments, subunits, and artificial analogs thereof.
Those regions o~ the HSP70 molecule which show the greatest structural similarity between different organisms and species are contemplated to be the key sources o~ its biological activity. Therefore, fragments of the native protein, analogs which contain substitution mutations, deletion mutations, or addition mutations, or even entirely synthetic analogs of HSP70, can be prepared in accordance with known procedures and tested in a routine manne~ for their ability to increase the metabolic stress tolerance of a sample of tissue or cells using the procedures described herein.
Dose of hsp70 will vary depending on the particular route of administration used. In general, for systemic, local, and ln vitro treatments, an overall dose range of from about .02 milligrams to about 20 milligrams , . , ' .
. - , . .
' ' ' ~ : ' ' ~ ' ' , - . . .. , . , :
!: ' ' 2079~
hsp70 per gram of cells or tissue being treatea`~is contemplated. It is further contemplated that, for local treatments, the maximum doses will be about twenty times - greater than the maximum systemic doses.
HSP70 may be administered concurrently or i~
combination with other therapeutic agents. For example~
the HSP70 may be combined with another agent known to protect cells from acute injury. Such agents include anti-oxidants or free radical scavengers such as vitamins lo C and E and superoxide dismutase whlen the damaging event works through the production of reactive oxygen molecules. When the mechanism of cell damage involves the influx of extracellular calcium, tha other agent might be one which reduces the influx of excess calcium ions (e.g., in brain tissue) such as dextrorphan and MK-801. When the mechanism of damage is myocardial infarction/ the other agent might be one that removes the blockage of blood flow to the heart muscle, such as tissue plasminogen activator (TPA) and streptokinase.
Hsp70 may be administered per se or in the form of a pharmaceutically ac~eptable salt. When used in medicine, the salts of hsp70 should be both pharmacologically and pharmaceutically acceptablel but non-pharmaceutically acceptable salts may conveniently be used to prepare the free active compound or pharmaceutically acceptable salts thereof and are not excluded from the scope of this invention. Such pharmacologically and pharmaceutically acceptable salts include, but are not limited to, those prepared from the following acids: hydrochloric, hydrobromic, sulphuric, nitric, phosphoric, maleic, acetic, salicylic, p-toluenesulfonic, tartaric, citric, methanesulphonic, formic, malonic, succinic, naphthalene-2-sulphonic and benzenesulphonic. Also, pharmaceutically acceptable salts can be prepared as alkaline metal or alkaline earth salts, such as sodium, potassium or calcium salts of the carboxylic acid group. Thus, ~he present in~ent:io~ also . ' `
.. . , . . . ~ .
2~7~813 provides pharmaceutical formulations, both Eor vete~ nary and ~or human medical use, which comprise hsp70 together with one or more pharmaceutically acceptable carriers thereof and optionally any other therapeutic ingredients.
S The carrier(s) must be pharmaceutically acceptable in the sense of being compatible with the other ingredients o~
the formulation and not unduly deleterious to the recipient thereo~.
The formulations include those suitable for lo oral, rectal, topical, nasal, opht:halmic or paxenteral (including subcutaneous, intramuscular and intravenous) administration, all of which may ~e used as routes of administration for practicing the present inventionO
Ot~er suitable routes of administration include intrathecal administration directly into spinal fluid (CSF), direct injection onto an arterial surface to prevent re-stenosis, and intraparenchymal injection directly into targeted areas of an organ. Formulations suitable for parenteral administration are preferred.
The formulations may conveniently be presented in unit dosage form and may bs prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing the active compound into association with a carrier which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing the active compound into association with a liquid carrier, a ~inely divided solid carrier, or both, and then, if necessary, shaping the product into desired ~ormulations.
Formulations of the present invention suitable for oral administration may be presented as discrete units such as capsules, cachets, tablets or lozenges, each containing a predetermined amount o~ thP
potentiating agent as a powder or granules; as liposomes containing hsp70; or as a suspension in an aqueous liquor or non-aqueous liquid such as a syrup, an elixir, an emulsion or a draught. -:
: . .
. . ! 2 0 7 9 8 1 3 ; , . ` . ~
` ` A tablet may be made by compression or molding, optionally with one or more accessory ingredients.
Compressed tablets may be prepared by compressing in a suitable machine, with the active compound being in a free-flowing form such as a powder or granules which is optionally mixed with a binder, disintegrant, lubricant, inert diluent, surEace active agent or dispersing agent~
Molded tablets comprised of a mixture of the powdered active compound with a suitable carrier may be made by molding in a suitable machine.
A syrup may be made by adding the active compound to a concentrated agueous solution of a sugar, for example sucrose to which may also be added any accessory ingredient~s). Such azcessory ingredient(s) may include flavorings, suitable preservatives, an agent to retard crystallization of the sugar, and an agent to increase the solubility of any other ingredient, such as a polyhydric alcohol, for example glycerol or sorbitol.
Formulations suitable for parenteral administration conveniently comprise a sterile aqueous preparation of the active compound, which is preferably isotonic with the blood of the recipient.
Nasal spray formulations comprise purified aqueous solutions of the active compound with preservative agents and isotonic agents. Such formulations are preferably adjusted to a p~ and isotonic state compatible with the nasal mucous membranes.
Formulations for rectal administration may be presented as a suppository with a suitable carrier such as cocoa butter, or hydrogenated ~ats or hydrogenated fatty carboxylic acids.
Ophthalmic formulations are prepared by a similar method to the nasal spray, except that the pH and isotonic factors are preferably adjusted to match that of the eyeO
Topical formulation~ comprise the active c~mpound dissolve~! or suspended in o~e or more media such .- , . : .:
: , 2 ~ 7~
"~. .
as mineral oil,~pe~r^oleum, polyhydroxy alcohols or other bases used for topical pharmaceutical formulations. The addition of other accessory ingredients, vide infra, may be desirable.
In addition to the aforem~entioned ingredients, the formulations of this invention may further include one or more accessory ingredient(s) selected from diluents, buffers, flavoring agents, binders, disintegrants, surface active agents, thickeners, lubricants, preservatives (including antioxidants) and the like.
The following Examples are provided to illustrate the present invention, and should not be construed as limiting thereof. Temperatures are given in degrees Celsius unless otherwise indicated.
Effect of h~p70 on 8urvival o~ Aortic Cell~ fro~
Normal and Athero3clerotic C~no~oloqu~ Nacaques A. METHODS
1. Materials.
Low calcium (O.2 mM) Hank's balanced salt solution (LC-HBSS) supplemented with essential and nonessential amino acids, penicillin (100 IU/ml~, streptomycin (100 ~g/ml), and phenol red indicator, and special low calcium Hank's balanced salt solution (SL-HLSS) without amino acids or phenol red,_where prepared ~resh prior to use in accordance with known techniques.
See N. Haley et al., Lab Invest. 37, 287 (1977).
Chromatographically purified collagenase and elastase were obtained from Worthington Diagnostics (Freehold, NJt USA). Soybean trypsin inhibitor (crude) was from Millipore, Inc. (Bedford, MA, USA~. The 4-methylumbeliferyl-2-acetimido-2-deoxy-~ D-glucopyra~oside ~MW 379.37) substra~e ~or N-acetyl-~-glucosaminidase (NABA) enzyme activity assays was from Koch-Light Laboratories (Coinbrigbt-Bucks, UK). The hsp70 employed was purifie~ fro~ bovinP br~in essentially according to .. . . . .
: . . . . ~: :
I ! ~
2079~13 ~.. , ~ ' .
.. -15-the procedu;e of Schlossman et al., 99 J. Cell Biol. 723 tl984). The hsp70 and N27F34 monoclonal antibody were gifts from Dr. Lawrence Hightower (University o~
Connecticut, Storrs) and Dr. William Welch (University of ' 5 California, San Francisco), respectively. The horseradish peroxidase-conjugated secondary antibody for Western blot analysis and lactate clehydrogenase, histone H-IIa, and parathyroid hormone for comparison against hsp70 were from Sigma Chemicals (S1:. Louis, Mo, USA).
2. Induction of Ath~erosclerosis.
Eight ad~lt male cynomolgus macaques were obtained from Charles River Laboratories, and housed in individual cages. Five animals were fed an atherogenic diet consisting of 1.0 mg cholesterol/kcal, with 40% of calories from butterfat, 38% of calories frnm carbohydrates, 22% of calories from protein, and 270 ml water/kg, D. Small et al., J. Clin. Invest. 73, 590 (1984). Three control animals were fed Purina0 Monkey Chow. Monkeys were fed these diets ad llbitum for 23-27 months. Periodic plasma lipid pro~iles were determined as a measure of success in induction o~
hypercholesterolemia (Table 1).
3. Animal Sacri~ice and Cell Isolation.
Animals were anesthetized with 0.2 cc o~
ketamine HC1 and 1.0 cc of sodium pentobarbital (IV).
Aortas were removed from the aortic arch to the iliac bif~rcation and held in normal saline at 4C. Adherent adventitia was dissected away and each aorta then opened and laid flat. Aortas were assessed visually for grade of atherosclerosis on a scale of O to IV, F. ParXer, G.
Oglund, Am. J. Pathol 48, 197 (1966), and for percent confluency (Table 1). Sections weighing approximately 1.0 g each wer~ dissected and minced to 250 ~m sguares using a McIlwain tissue chopper (Beckman Instruments, Fullerton, CA, US~)O The minced material was placed in 1.0 ml of LC-HBSS per 100 mg of tissue, which contained 600 U/ml collagenase, 5 U/ml elastase, and 1 mg/ml ..
; . " ' '' . . ~ " ' -i 2~79~3 soybean trypsin in~l~ito~. The digestion mix was incubated at 37~C, adding sodium carbonate as needed to maintain neutrality, and shaXing in a Dubnoff Metbolic incubator (Fisher, Pittsburgh, PA, IISA). Released cells were collected every 30 minutes, separated ~rom the enzyme mixture, washed twice with SL-HBSS for 6 minutes at 3000 rpm, and suspended in 2.0 ml of SL-HBSS at 4-C
until all cells were harvested. Ind:ividual harvests were pooled, the cell concentrations determined, and the isolate diluted to 1o6 cells/ml with SL-HBSS. The final diluted isolate was held at 4C prior to and after a treatment regimen.
.
, ~ ', . " : ' ~
- : ', '- :,, , , ' o 2079813 ,,; ~ ,. -p~esent invention, with ma~nall~n (e.g., dog, cat, human) cells and tissue particularly pre~erxed. The term "animal" as used herein, refers to the subjects of ~ veterinary medicine, such as dog, cat, cow, pig~ and horse.
~ Cells and tissue which are under stress are treated with hsp70 to combat mortality. For examplel cells which are maintained in culture (e.g., for the purpose of producing proteins or other materials from the cells) or tissue which is maintained in culture (e.g.0 complete organs such as heart, lung, liver or kidney prior to transplant) may be considered as "under stress"
for the purpose of practicing the present invention. For example, organs could be immersed in a solution containing HSP70, or a larger organ perfused through its vasculature, with an HSP70 solution. The HSP70 would be taken up by the cells of the organ, making them more resistant to the lack of blood, nutrients and other needed substances that exists once they are removed from the body. Likewise, the ~SP70 could be included in a reperfusion solution to combat tissue reperfusion injury.
The HSP70 may be added to known solutions and used in accordance with procedures known to those skilled in the art for these purposes. Such solutions and procedures are disclosed in U.S. Patent No. ~,920,044, titled "Intracellular Flush Solution for Preserving Organs", U~S. Patent No. 4,879,283 titled "Solutions ~or the Preservation of Organs", U.S. Patent No. 4,873,230 titled "Composition for the Preservation of Organs", and U.S.
Patent No. 4,798,824 titled "Perfusate for the Preservation of Organs". Applicants intend the disclosures of these and all other patents cited herein to be incorporated herein by reference.
Tissue under stress ln vivo may also be treated. For example, arterial and myocardial tissue may be treated by adminis~ering hsp70 during by-pass surgery to enhance the survivahility o~ cells ~n that tissue.
-. .
: ~ ;
. ! .:
-7- ~
Cardiac ischemi~ may ~e t:reated by a~min~stering hsp70 about the time of myocardial infarction to enhance the survivability of cells in those tissues. The kidney may be protected from damage from toxic substances such as the antibiotic Gentamicin by the administration of hsp700 :f!
Arterial tissue may be administered hsp70 during laser angioplasty and atherectomy to reduce damage to these tissues arising from such procedures.
Nerve tissue (i.e., peripheral nerve and central nerve) which is under stress in vivo may also be treated by the method of the present invention. For example, peripheral nerves which are severed are subject to retrograde degeneration, which degeneration may culminate in death of the nerve cell, or soma, if too great a portion of the nerve's axon is distal to the site of the cut. If degeneration does not culminate in cell death, then an opportunity exists for the nerve to regenerate. Thus, hsp70 may be administered to such nerve tissue, through administration to the host animal, to combat cell mortality which may result from the severing of the peripheral nerve.
Nerve tissue may also be subject to anoxic stress in vivo. For example, anoxic stress may arise -from a stroke or burst aneurism which damages nerve tissue by depriving the tissue of blood. When central nerve tissue is so damaged, the damage typically occurs in a watershed pattern in relation to the blood vessels:
tissue closest the damaged supply vessel is most severely damaged; tissue furthest from the damaged vessel which is supplied by other vessels is least severely damaged;
tissue intermediate of these extremes shows intermediate damage. Afflicted subjects are administered hsp70 to combat mortality in cells subject to this type of stress.
As noted above, the present invention may be employed to combat restenosis a~ter angioplasty.
Angioplasty is a procedure for dilating arteries which are occluded or blo~ked. In a typical transluminal ~ ' . ~ ' , : -2079~13 -"` ' "`" --E}--baloon angioplast~ procedure, a cath~ter ~hich carries an inflatable dilation balloon at the clistal end is employed to reshape a partially occluded arl-ery. The balloon is inserted in the deflated condition in the restricted portion of the artery and inflated so that the occluded lumen is reshaped by the dilation balloon to allow better passage o~ blood. The obstructing material is neither - dislocated nor removed from the vessel, but rather pressed against the wall. The wall, in turn, is stretched to accommodate the previously obstructing material. After the lumen has been reshaped, the dilation balloon is deflated and removed. The site of the formed obstruction may, however, become reoccluded when/if the vessel returns to its previous configuration:
a phenom~non known as "restenosis." A variety of angioplasty procedures and instruments are known. See e.q. U.S. Patent Nos. 4,838, 269 and 4,794,928 (the disclosures of which are to be incorporated herein by reference). A subject in need of treatment to prevent restenosis (i.e., either during angioplasty or after angioplasty prior to the onset of restenosis) may be treated by administering hsp70 to the lumen of the vessel which has been reshaped (e.g., by intraveneous injection or intraarterial injectionl. Any administration which places hsp70 into the bloodstream of the subject or at the site of treatment is suitable, but preferably the administration procedure will direct the hsp70 to the particular site of the angioplasty (i.e., the vessel wall which has been reshaped). For example, the hsp70 may be applied directly to the site of treatment by means of a sweating baloon catheter (i~e., an angioplasty balloon which is perforated so as to administer hsp70 through the perforations ~o the arterial cell wall during angioplasty).
Skin tissue under stress due to wounds, burns, ulcers, in~ections, and other types o~ traumatic injury may be treated by ~e me~hod o~ the present invsntion.
~l 2079~13 ~t ~
~ , _g _ For such purposes HSP70 may be administerea ~by~ ~opical application to the skin in the form o~ a salve o~ cream to enhance repair and healing of the tissue. Tissues may also be under stess due to chemotherapeutic treatment, as in cancer chemotherapy. In such cases HSP70 may be administered subsequent to the chemotherapeutic treatment as a "rescue" agent.
Hsp70 is a member of the hleat shock protein (or "hsp") family, which are produced when cells or organisms are exposed to elevated temperatures. This response has been observed in essentially all organisms to date. See ~enerally S. Lindquist, The Heat-Shock Response, Ann.
Rev. Biochem. 55, 1151 (1986). For example, hsp70 has been found in plants. See, e.q.. J. Marshall et al., ~roc. Natl. Acad. Sci. USA 87, 374 (1990). The hsp70 ~roup is the most highly conserved member o~ the hsp family. For example, the human protein is 73% identical to the Drosophila protein and is 50% identical to the corresponding Escherichia coli protein dnaK. See B.
Bukau et al., DnaK and GroE Proteins Play Roles in E.
coli Metabolism at Low and Intermediate Temperatures as Well as at High Temperatures, in Stress-Induced Proteins, 27 (1989)(published by Alan R. Liss, Inc.). Many of the di~ferences are merely homologous substitutions, and there are regions of homology which those in the ~ield consider to be extraordinary. S. Lindq~ist, supra at 1155-56.
Within some species, the term "hsp70" itself denotes a ~amily of closely related protein~, all found in that species. In Saccharomyces cerevisiae, strains bearing certain hsp70 mutations are nonviable, but viability can be restored by altering the transcriptional regulation o~ the remaining genes. See E. Craig st al., Complex Regulation of Three Heat Inducible hsp70 Related Genes in S~ccharomyces cerevisiae, in Stress-Induced Proteins, 51 ~1989). In view of the biological interchangeability and hsmolo~y, any membe~ of the hsp70 . ~ ' ' `' . . '' , . ' : . - . :' ' : .
2~79gl3 ': ` i ! ~
family within a species is contemplate~ as useful in practicing the p~esent invention.
As to species of origin, in view o~ the highly conserved nature of the hsp70 family among broadly divergent species, hsp70 from any species of origin is contemplated as useful in praclicing the present invention tnumerous references to hsp70 are set forth above, the disclosures of which are ~o be incorporated herein by reference). Thus, animal, plant ~e.g., Pisum sativum), and bacterial hsp70 are all contemplated as useful for treating cells or tissue of any origin in practicing the present invention. It is, nevertheless, contemplated that an hsp70 of related origin to the cell or tissue being treated will be preferred for practicing the present invention. For example, plant hsp70 is contemplated as preferred for treating plant cells or tissue, animal hsp70 is contemplated as preferred for treating animal cells or tissue, mammalian hsp70 is contemplated as preferred for treating mammalian cells or tissue, and so on.
The term 'IHSP 70" is intended to include active fragments, subunits, and artificial analogs thereof.
Those regions o~ the HSP70 molecule which show the greatest structural similarity between different organisms and species are contemplated to be the key sources o~ its biological activity. Therefore, fragments of the native protein, analogs which contain substitution mutations, deletion mutations, or addition mutations, or even entirely synthetic analogs of HSP70, can be prepared in accordance with known procedures and tested in a routine manne~ for their ability to increase the metabolic stress tolerance of a sample of tissue or cells using the procedures described herein.
Dose of hsp70 will vary depending on the particular route of administration used. In general, for systemic, local, and ln vitro treatments, an overall dose range of from about .02 milligrams to about 20 milligrams , . , ' .
. - , . .
' ' ' ~ : ' ' ~ ' ' , - . . .. , . , :
!: ' ' 2079~
hsp70 per gram of cells or tissue being treatea`~is contemplated. It is further contemplated that, for local treatments, the maximum doses will be about twenty times - greater than the maximum systemic doses.
HSP70 may be administered concurrently or i~
combination with other therapeutic agents. For example~
the HSP70 may be combined with another agent known to protect cells from acute injury. Such agents include anti-oxidants or free radical scavengers such as vitamins lo C and E and superoxide dismutase whlen the damaging event works through the production of reactive oxygen molecules. When the mechanism of cell damage involves the influx of extracellular calcium, tha other agent might be one which reduces the influx of excess calcium ions (e.g., in brain tissue) such as dextrorphan and MK-801. When the mechanism of damage is myocardial infarction/ the other agent might be one that removes the blockage of blood flow to the heart muscle, such as tissue plasminogen activator (TPA) and streptokinase.
Hsp70 may be administered per se or in the form of a pharmaceutically ac~eptable salt. When used in medicine, the salts of hsp70 should be both pharmacologically and pharmaceutically acceptablel but non-pharmaceutically acceptable salts may conveniently be used to prepare the free active compound or pharmaceutically acceptable salts thereof and are not excluded from the scope of this invention. Such pharmacologically and pharmaceutically acceptable salts include, but are not limited to, those prepared from the following acids: hydrochloric, hydrobromic, sulphuric, nitric, phosphoric, maleic, acetic, salicylic, p-toluenesulfonic, tartaric, citric, methanesulphonic, formic, malonic, succinic, naphthalene-2-sulphonic and benzenesulphonic. Also, pharmaceutically acceptable salts can be prepared as alkaline metal or alkaline earth salts, such as sodium, potassium or calcium salts of the carboxylic acid group. Thus, ~he present in~ent:io~ also . ' `
.. . , . . . ~ .
2~7~813 provides pharmaceutical formulations, both Eor vete~ nary and ~or human medical use, which comprise hsp70 together with one or more pharmaceutically acceptable carriers thereof and optionally any other therapeutic ingredients.
S The carrier(s) must be pharmaceutically acceptable in the sense of being compatible with the other ingredients o~
the formulation and not unduly deleterious to the recipient thereo~.
The formulations include those suitable for lo oral, rectal, topical, nasal, opht:halmic or paxenteral (including subcutaneous, intramuscular and intravenous) administration, all of which may ~e used as routes of administration for practicing the present inventionO
Ot~er suitable routes of administration include intrathecal administration directly into spinal fluid (CSF), direct injection onto an arterial surface to prevent re-stenosis, and intraparenchymal injection directly into targeted areas of an organ. Formulations suitable for parenteral administration are preferred.
The formulations may conveniently be presented in unit dosage form and may bs prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing the active compound into association with a carrier which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing the active compound into association with a liquid carrier, a ~inely divided solid carrier, or both, and then, if necessary, shaping the product into desired ~ormulations.
Formulations of the present invention suitable for oral administration may be presented as discrete units such as capsules, cachets, tablets or lozenges, each containing a predetermined amount o~ thP
potentiating agent as a powder or granules; as liposomes containing hsp70; or as a suspension in an aqueous liquor or non-aqueous liquid such as a syrup, an elixir, an emulsion or a draught. -:
: . .
. . ! 2 0 7 9 8 1 3 ; , . ` . ~
` ` A tablet may be made by compression or molding, optionally with one or more accessory ingredients.
Compressed tablets may be prepared by compressing in a suitable machine, with the active compound being in a free-flowing form such as a powder or granules which is optionally mixed with a binder, disintegrant, lubricant, inert diluent, surEace active agent or dispersing agent~
Molded tablets comprised of a mixture of the powdered active compound with a suitable carrier may be made by molding in a suitable machine.
A syrup may be made by adding the active compound to a concentrated agueous solution of a sugar, for example sucrose to which may also be added any accessory ingredient~s). Such azcessory ingredient(s) may include flavorings, suitable preservatives, an agent to retard crystallization of the sugar, and an agent to increase the solubility of any other ingredient, such as a polyhydric alcohol, for example glycerol or sorbitol.
Formulations suitable for parenteral administration conveniently comprise a sterile aqueous preparation of the active compound, which is preferably isotonic with the blood of the recipient.
Nasal spray formulations comprise purified aqueous solutions of the active compound with preservative agents and isotonic agents. Such formulations are preferably adjusted to a p~ and isotonic state compatible with the nasal mucous membranes.
Formulations for rectal administration may be presented as a suppository with a suitable carrier such as cocoa butter, or hydrogenated ~ats or hydrogenated fatty carboxylic acids.
Ophthalmic formulations are prepared by a similar method to the nasal spray, except that the pH and isotonic factors are preferably adjusted to match that of the eyeO
Topical formulation~ comprise the active c~mpound dissolve~! or suspended in o~e or more media such .- , . : .:
: , 2 ~ 7~
"~. .
as mineral oil,~pe~r^oleum, polyhydroxy alcohols or other bases used for topical pharmaceutical formulations. The addition of other accessory ingredients, vide infra, may be desirable.
In addition to the aforem~entioned ingredients, the formulations of this invention may further include one or more accessory ingredient(s) selected from diluents, buffers, flavoring agents, binders, disintegrants, surface active agents, thickeners, lubricants, preservatives (including antioxidants) and the like.
The following Examples are provided to illustrate the present invention, and should not be construed as limiting thereof. Temperatures are given in degrees Celsius unless otherwise indicated.
Effect of h~p70 on 8urvival o~ Aortic Cell~ fro~
Normal and Athero3clerotic C~no~oloqu~ Nacaques A. METHODS
1. Materials.
Low calcium (O.2 mM) Hank's balanced salt solution (LC-HBSS) supplemented with essential and nonessential amino acids, penicillin (100 IU/ml~, streptomycin (100 ~g/ml), and phenol red indicator, and special low calcium Hank's balanced salt solution (SL-HLSS) without amino acids or phenol red,_where prepared ~resh prior to use in accordance with known techniques.
See N. Haley et al., Lab Invest. 37, 287 (1977).
Chromatographically purified collagenase and elastase were obtained from Worthington Diagnostics (Freehold, NJt USA). Soybean trypsin inhibitor (crude) was from Millipore, Inc. (Bedford, MA, USA~. The 4-methylumbeliferyl-2-acetimido-2-deoxy-~ D-glucopyra~oside ~MW 379.37) substra~e ~or N-acetyl-~-glucosaminidase (NABA) enzyme activity assays was from Koch-Light Laboratories (Coinbrigbt-Bucks, UK). The hsp70 employed was purifie~ fro~ bovinP br~in essentially according to .. . . . .
: . . . . ~: :
I ! ~
2079~13 ~.. , ~ ' .
.. -15-the procedu;e of Schlossman et al., 99 J. Cell Biol. 723 tl984). The hsp70 and N27F34 monoclonal antibody were gifts from Dr. Lawrence Hightower (University o~
Connecticut, Storrs) and Dr. William Welch (University of ' 5 California, San Francisco), respectively. The horseradish peroxidase-conjugated secondary antibody for Western blot analysis and lactate clehydrogenase, histone H-IIa, and parathyroid hormone for comparison against hsp70 were from Sigma Chemicals (S1:. Louis, Mo, USA).
2. Induction of Ath~erosclerosis.
Eight ad~lt male cynomolgus macaques were obtained from Charles River Laboratories, and housed in individual cages. Five animals were fed an atherogenic diet consisting of 1.0 mg cholesterol/kcal, with 40% of calories from butterfat, 38% of calories frnm carbohydrates, 22% of calories from protein, and 270 ml water/kg, D. Small et al., J. Clin. Invest. 73, 590 (1984). Three control animals were fed Purina0 Monkey Chow. Monkeys were fed these diets ad llbitum for 23-27 months. Periodic plasma lipid pro~iles were determined as a measure of success in induction o~
hypercholesterolemia (Table 1).
3. Animal Sacri~ice and Cell Isolation.
Animals were anesthetized with 0.2 cc o~
ketamine HC1 and 1.0 cc of sodium pentobarbital (IV).
Aortas were removed from the aortic arch to the iliac bif~rcation and held in normal saline at 4C. Adherent adventitia was dissected away and each aorta then opened and laid flat. Aortas were assessed visually for grade of atherosclerosis on a scale of O to IV, F. ParXer, G.
Oglund, Am. J. Pathol 48, 197 (1966), and for percent confluency (Table 1). Sections weighing approximately 1.0 g each wer~ dissected and minced to 250 ~m sguares using a McIlwain tissue chopper (Beckman Instruments, Fullerton, CA, US~)O The minced material was placed in 1.0 ml of LC-HBSS per 100 mg of tissue, which contained 600 U/ml collagenase, 5 U/ml elastase, and 1 mg/ml ..
; . " ' '' . . ~ " ' -i 2~79~3 soybean trypsin in~l~ito~. The digestion mix was incubated at 37~C, adding sodium carbonate as needed to maintain neutrality, and shaXing in a Dubnoff Metbolic incubator (Fisher, Pittsburgh, PA, IISA). Released cells were collected every 30 minutes, separated ~rom the enzyme mixture, washed twice with SL-HBSS for 6 minutes at 3000 rpm, and suspended in 2.0 ml of SL-HBSS at 4-C
until all cells were harvested. Ind:ividual harvests were pooled, the cell concentrations determined, and the isolate diluted to 1o6 cells/ml with SL-HBSS. The final diluted isolate was held at 4C prior to and after a treatment regimen.
4. Confirmation and Characterization of hsp70.
Bovine brain hsp70 was received as a solutio~
of 10 ~g/~l in 20 mM HEPES buffer, pH 700 and routinely stored at -30 C. The composition was confirmed using Western blot analysis. Samples of protein were separated on 10% polyacrylamide gel under reducing conditions, blotted to nitrocellu}ose, and reacted with N27F34, a murine monoclonal antibody specific to the 73 kD
constituitive and 72 kD inducible hsps. The secondary antibody was horseradish peroxidase-conjugated, rabbit anti-mouse anti-IgG. Final staining was with diaminobenzidine/hydrogen peroxide in Tris bu~fer, pH
7.2. Relative densities of the identified protein bands were determined using an Ultroscan XL ~aser densitometer (LKB, Rockville, MD. USA).
Bovine brain hsp70 was received as a solutio~
of 10 ~g/~l in 20 mM HEPES buffer, pH 700 and routinely stored at -30 C. The composition was confirmed using Western blot analysis. Samples of protein were separated on 10% polyacrylamide gel under reducing conditions, blotted to nitrocellu}ose, and reacted with N27F34, a murine monoclonal antibody specific to the 73 kD
constituitive and 72 kD inducible hsps. The secondary antibody was horseradish peroxidase-conjugated, rabbit anti-mouse anti-IgG. Final staining was with diaminobenzidine/hydrogen peroxide in Tris bu~fer, pH
7.2. Relative densities of the identified protein bands were determined using an Ultroscan XL ~aser densitometer (LKB, Rockville, MD. USA).
5. Induced Stress of Cell Isolates.
Normal and diseased arterial cell isolates were tested for changes in viability and structure-linked latency of lysosomal enzymes, in response to extended stress. Samples of 0.2 ml of cell isolates were placed in sealed 1 ml Eppendorf tubes with 0.01 ml of SL-~BSS
with or withou~ hsp70 added. Dose-response ~or hsp70 was determined using cells exposed to 37-C for 20 hours, with and without 2, 5, 10, or 100 ng hsp70 added per 103 cells.
To det~rmine responses following thermal-induced stress, ., . ' . . :. , , ~ :
,: ; ,. .~
20798~3 ~- cells were exposed to 23, 37, or 451C for ~0 hours, with - or without 10 ng of hsp70 added per 103 cells.
- Comparative studies for nonspecific changes due to exogenous protein were performed at 37C using lactate dehydrogenase, histone H-IIa, and parathyroid hormone, at normal and ten times normal physiological concentrations.
Normal and diseased arterial cell isolates were tested for changes in viability and structure-linked latency of lysosomal enzymes, in response to extended stress. Samples of 0.2 ml of cell isolates were placed in sealed 1 ml Eppendorf tubes with 0.01 ml of SL-~BSS
with or withou~ hsp70 added. Dose-response ~or hsp70 was determined using cells exposed to 37-C for 20 hours, with and without 2, 5, 10, or 100 ng hsp70 added per 103 cells.
To det~rmine responses following thermal-induced stress, ., . ' . . :. , , ~ :
,: ; ,. .~
20798~3 ~- cells were exposed to 23, 37, or 451C for ~0 hours, with - or without 10 ng of hsp70 added per 103 cells.
- Comparative studies for nonspecific changes due to exogenous protein were performed at 37C using lactate dehydrogenase, histone H-IIa, and parathyroid hormone, at normal and ten times normal physiological concentrations.
6. Assessment of Cell Viability_and Lysosomal Membrane _nteqrity.
Cell viability was determined immediately - 10 following the 20 hour test period using 0.~ Trypan blue dye exclusion. Each stored cell suspension was sampled in quadruplicate and examined individually by two investigators. Intact cells versus cell lysis also were noted. Structure-linked latency of lysosomal N-acetyl-~-glucosaminidase (NABA) was calculated as representative of lysosomal membrane integrity. Free and total NABA
activities were determined fluorometrically as described previously. See P. Berberian, S. Fowler, ExP. Mol.
Pathol. 30, 27 (1979). Briefly, samples of 0.1 ml of experimental aortic cells were suitably diluted in SL-HBSS, and incubated 90 minutes at 37-C with 0.1 ml of 0.50 mM 4-methylumbelliferone substrate in 250 mM sucrose containing 100 mM sodium citrate buffer, pH 4.8, with (total activity) or without (free activity) 0.1% Triton X-100. Structure-linked latency of lysosomal enzymes was de~ined by the difference between total and free NABA
activity, and was expressed as a percent of total activity, J. Berthet et al., Biochem. J. 50, 182 (1952).
Cell viability was determined immediately - 10 following the 20 hour test period using 0.~ Trypan blue dye exclusion. Each stored cell suspension was sampled in quadruplicate and examined individually by two investigators. Intact cells versus cell lysis also were noted. Structure-linked latency of lysosomal N-acetyl-~-glucosaminidase (NABA) was calculated as representative of lysosomal membrane integrity. Free and total NABA
activities were determined fluorometrically as described previously. See P. Berberian, S. Fowler, ExP. Mol.
Pathol. 30, 27 (1979). Briefly, samples of 0.1 ml of experimental aortic cells were suitably diluted in SL-HBSS, and incubated 90 minutes at 37-C with 0.1 ml of 0.50 mM 4-methylumbelliferone substrate in 250 mM sucrose containing 100 mM sodium citrate buffer, pH 4.8, with (total activity) or without (free activity) 0.1% Triton X-100. Structure-linked latency of lysosomal enzymes was de~ined by the difference between total and free NABA
activity, and was expressed as a percent of total activity, J. Berthet et al., Biochem. J. 50, 182 (1952).
7. Statistical Methods.
The results were analyzed for dif~erences in cell viability and structure-linked lysosomal enzyme latency using repeated measures ANOVA. Samples were compared for effects of disease versus control aortic cells, dosage o~ heat shock protein added, and temperature during test incubation. The interrelationship of viability and latency was tested using standard linear regression.
.
.
' ' . ' ' : ' , "-: - . :
.:: : - . : .
$~
B. RESULTS
- 1. Dietar~ Induction of Atherosclerosis : The atherogenic diet induced hypercholesterolemia with subsequent plaque formation, as 5 shown in Table 1. Light and electron microscopic examination of cell isolates from diseased aortas contained a large proportion of lipid-filled îoam cells and lipid-enriched smooth muscle cells as w~ll as normal smooth muscle cells. Normal aortas exhibited no lesions, 10 and their respective cell isolate.s contained primarily normal smooth muscle cells.
TAE~LE 1 Monkey Blood Lipid Values and Atherosclerosis Grade Athero- Conflu-15Monkeygenic ency No. Diet Chol.1 HDL1 TG1 Grade2 96 Yes 778 15 16II-III 70 2 Yes 572 33 21II 30 3 Yes 672 40 92III . 100 20 4 No 112 65 23 0 -- -, 5 No 142 66 28 0 --6 No 183 100 27 0 --1 Plasma v~lues arcfrom pre-sacnf ce, fasted an7mals, and ar~ e~pr~ssed ~s mg/dL Chol. = total 2 5 plasma -~
~hol~terol; HDL = total plasn~a high~ensity lipoproteu~s; 7G = total plasma tng~ceri~les.
~ Grade: O = No lesi~ns; 11 = Miniinal~y rais~d atherontatous lesions; Ill = Signif cant~y raised atheromatous lesions, with f bros~s.
2. Characterization of hsp70.
Western blot analysis O:e the purified hsp70 used in these studie:; yielded two immunoreactive bands, corresponding to the 73 kD constituitive (estimated 70%
of total reactive protein) and 72 kD induced ~estimated 30% of total reactive protein) forms of hspO
.... .
.
,:, : ., . : .. . . .
2~79813 ~`~ 3. Effect of Thermal-Induced Stress U~on Viability and Ly~osomal Membrane In~tegrity o~f Isolated Cells.
Since data analyses using repeated measures ANOVA did not show any significant differences in test responses between cell isolates from normal and diseased animals, the isolates were considered similar in their response, and the data discussed pooled for analysis (n = 6). A linear regression of structure-linked latency of lysosomal enzymes (i.e., lysosomal membrane integrity) versus viability for control (No hsp70) aortic cell isolates (n = 23) showed lysosomal membrane integrity and viability were well correlated (r = 0.85), regardless of incubation temperature (Fig. 1). Furthermore, viability and lysosomal membrane integrity of control samples both declined significantly (p < 0.0005 and < 0.004, respectively) as incubation temperature rose (Fig. 2a &
b). Treatment with hsp70, however, produced disproportionate effects upon these two parameters.
The response of isolated cells at 37'C for 20 hours to hsp70 showed a significant increase (p < 0.05) in viability at or above 10 ng hsp70 per 103 cells (Fig.
3), compared to cells without added hsp. No change in v-iability occurred even with a ten-fold increase in the dose to 100 ng hsp70 per 103 cells. Temperature-response studies showed 10 ng hsp70 per 103 cells increased cell viability (p < 0.05) after storage for 20 hours at all three temperatures tested, with the greatest effect pxesent at 37-C tFig. 4). Based on these results, the optimum temperature for resolution of long-term (i.e., 20 hours) ef~ects of added hsp was 37~C. In contrast, no effect of hsp70 vn lysosomal membrane integrity was evident for the doses of added hsp or temperature range tested (Fig. 5). Studies at 37-C of three control proteins tested individually for non-specific exogenous effects each failed to show a maintenance of viability or .
.. . . . . .
~, .,: .. , . : . - . :
. :
.
l~ 2~79~13 ~20-`~lysosomal membrane integrity, at either normal or ten times normal physiological concentrations.
C. DISCUSSION
The data presented here showed that exogenous hsp70 can enhance arterial cell survival. The use of a relatively long test period at a physiological temperature as the stress parameter appears unique to the study. Previous hsp studias have used brief periods (15-90 minutes) at relatively high temperatures (42-45-) to stress cells or animals, M. Schlesinger et al., Cold Spring Harbor Laboratory, 1982; M. Pardue et al., Alan R.
Liss, Inc. (1989). In contrast, atherosclerotic plaques ;represent a system of chronic, multiple stresses. To more closely parallel these conditions, and especially those found in the necrotic core of a plaque, the present studies stressed cells by a combination of enzymatic cell release, hypoxia, low amino acid levels, and longer incubation periods.
Statistical differences were not cbserved in the test responses between normal and diseased arterial cell isolates. This may reflect the limited population size of this study, and/or the limited extent of atherosclerosis, i.e., the lack of arterionecrosis in these animals. Additionally, the procedure employed for cell release and the test conditions applied in this study may have caused a maximal hsp response for both normal and diseased cell isolates, masking differences in hsp responses present ln vivo. The large proportion of normal smooth muscle cells found in even the most diseased aortas might also have a masking effect. The lack of differences could a}so reflect the potential point of action for exogenous hsp. I hsp affects viability via plasmalemma effector sites whose composition or number do not change during atherogenesis, the reaction cells to exogenous hsp would be the same regardless of their level of lipid loadO Thus; the : ' ~ ' ' ' .
! . ~ ' ." ' ' . ,;' ' . ' ' ' .
! ,;' 2 ~ 7 ~
~ ~ results given here indicate a possible common pathway for the effect of exogenous hsp on arterial cells.
Viability and lysosomal membrane integrity are well correlated normally over a range o~ temperatures (Fig. l), but have discordant responses to exogenous hsp70. The positive effect of added hsp70 on viability of cell isolates was initiated by as little as 10 ng/103 cells and, once a significant effect was obtained, a ten fold increase in hsp concentration failed to induce further changes in cell viability (Fig. 3). This increase occurred over a range of temperatures, but was most significant at 37C (Fig. 4~, possibly due to a maximal activation of degradative enzymes in the cells under study at this temperature.
In contrast to cellular viability, lysosomal membrane integrity was not significantly changed by exogenous hsp70 (Fig. 5-). This observation may reflect a time-dependent factor yet to be determined. Figure 5 indicates that a decline in structure-linked lysosomal latency with temperature occurred for samples both with and without added hsp. If lysosomal NABA latency is an earlier marker than viability ~or membrane integrity in this system, measurements at time points before 20 hours may reveal changes in latency across all temperatures which are comparable to later changes in viability. To address this, time response studies are currently underway. Alternately, hsp70 may affect cell viability by a mechanism more specific than general cell membrane stabilization. If so, structure-linked lysosomal latency may be affected independently of viability or be unaf~ected by exogenous hsps.
E~UUMP~E 2 Prote~tion of Nerve ~is~ue ~lth H~P70 This experime~t was conducted to demonstrate the use of hsp70 to protect nerve tissue against damage using light damage in the rat retina as a model system.
Procedures were essentially as described in M. Barbe et ' .
. ~
~ ~ al., Science 241, 1817 (1988). hsp70 was as described ln connection with Example 1 above.
TWQ groups of three rats each received an in~ection into the vitreous chamber of the right eye of a saline solution that contained either 2 ~g or 10 ~g of purified hsp70. These rats al~o received in the left eye an injection of the saline solution alone to control for any effect the injection itself might have. A third group of two rats were not injected and served as untreated controls. A11 three groups were exposed to 175-200 foot-candles of fluorescent light beginning four hours after the injections and continuing for 24 hoursO
Two weeks after the light exposure, the eyes of each rat were prepared ~or routine histology and the nw~er o~
surviving photoreceptors in each eye determined by standard techniques. The difference in surviving photoreceptors between the right and left retinas was then calculated. A protective effect of the injected hsp70 is indicated when that difference is significantly greater than zero. On the other hand, if there was no effect of the injected hsp70, the loss of photoreceptors from the right and left eyes should average out to the same, giving a right-left difference that is not significantly different from zero.
Results are summarized in Figure 6. Based on a number of statistical comparisons, the group that received the 10 ug dose of Hsp70 showed significant protection of the retinal photoreceptors against the light damage (p~.05), with the right eye having about 36%
more photoreceptors than the }eft eye. The group that received the 2 ug dose of Hsp70 showed a trend in the same direction as the higher dose group, but it did not attain statistical significance with the small number of subjects tested.
The foregoing examples are illustrative of the present invention, and are not to be construed as limiting thereof. The in~ention is defined hy the 2~798~L3 --23~
:
~following claims, with equivalents of the claims to be in ::luded therein .
, .
''' .,~ .
, ; , ~` ` ' . ' '
The results were analyzed for dif~erences in cell viability and structure-linked lysosomal enzyme latency using repeated measures ANOVA. Samples were compared for effects of disease versus control aortic cells, dosage o~ heat shock protein added, and temperature during test incubation. The interrelationship of viability and latency was tested using standard linear regression.
.
.
' ' . ' ' : ' , "-: - . :
.:: : - . : .
$~
B. RESULTS
- 1. Dietar~ Induction of Atherosclerosis : The atherogenic diet induced hypercholesterolemia with subsequent plaque formation, as 5 shown in Table 1. Light and electron microscopic examination of cell isolates from diseased aortas contained a large proportion of lipid-filled îoam cells and lipid-enriched smooth muscle cells as w~ll as normal smooth muscle cells. Normal aortas exhibited no lesions, 10 and their respective cell isolate.s contained primarily normal smooth muscle cells.
TAE~LE 1 Monkey Blood Lipid Values and Atherosclerosis Grade Athero- Conflu-15Monkeygenic ency No. Diet Chol.1 HDL1 TG1 Grade2 96 Yes 778 15 16II-III 70 2 Yes 572 33 21II 30 3 Yes 672 40 92III . 100 20 4 No 112 65 23 0 -- -, 5 No 142 66 28 0 --6 No 183 100 27 0 --1 Plasma v~lues arcfrom pre-sacnf ce, fasted an7mals, and ar~ e~pr~ssed ~s mg/dL Chol. = total 2 5 plasma -~
~hol~terol; HDL = total plasn~a high~ensity lipoproteu~s; 7G = total plasma tng~ceri~les.
~ Grade: O = No lesi~ns; 11 = Miniinal~y rais~d atherontatous lesions; Ill = Signif cant~y raised atheromatous lesions, with f bros~s.
2. Characterization of hsp70.
Western blot analysis O:e the purified hsp70 used in these studie:; yielded two immunoreactive bands, corresponding to the 73 kD constituitive (estimated 70%
of total reactive protein) and 72 kD induced ~estimated 30% of total reactive protein) forms of hspO
.... .
.
,:, : ., . : .. . . .
2~79813 ~`~ 3. Effect of Thermal-Induced Stress U~on Viability and Ly~osomal Membrane In~tegrity o~f Isolated Cells.
Since data analyses using repeated measures ANOVA did not show any significant differences in test responses between cell isolates from normal and diseased animals, the isolates were considered similar in their response, and the data discussed pooled for analysis (n = 6). A linear regression of structure-linked latency of lysosomal enzymes (i.e., lysosomal membrane integrity) versus viability for control (No hsp70) aortic cell isolates (n = 23) showed lysosomal membrane integrity and viability were well correlated (r = 0.85), regardless of incubation temperature (Fig. 1). Furthermore, viability and lysosomal membrane integrity of control samples both declined significantly (p < 0.0005 and < 0.004, respectively) as incubation temperature rose (Fig. 2a &
b). Treatment with hsp70, however, produced disproportionate effects upon these two parameters.
The response of isolated cells at 37'C for 20 hours to hsp70 showed a significant increase (p < 0.05) in viability at or above 10 ng hsp70 per 103 cells (Fig.
3), compared to cells without added hsp. No change in v-iability occurred even with a ten-fold increase in the dose to 100 ng hsp70 per 103 cells. Temperature-response studies showed 10 ng hsp70 per 103 cells increased cell viability (p < 0.05) after storage for 20 hours at all three temperatures tested, with the greatest effect pxesent at 37-C tFig. 4). Based on these results, the optimum temperature for resolution of long-term (i.e., 20 hours) ef~ects of added hsp was 37~C. In contrast, no effect of hsp70 vn lysosomal membrane integrity was evident for the doses of added hsp or temperature range tested (Fig. 5). Studies at 37-C of three control proteins tested individually for non-specific exogenous effects each failed to show a maintenance of viability or .
.. . . . . .
~, .,: .. , . : . - . :
. :
.
l~ 2~79~13 ~20-`~lysosomal membrane integrity, at either normal or ten times normal physiological concentrations.
C. DISCUSSION
The data presented here showed that exogenous hsp70 can enhance arterial cell survival. The use of a relatively long test period at a physiological temperature as the stress parameter appears unique to the study. Previous hsp studias have used brief periods (15-90 minutes) at relatively high temperatures (42-45-) to stress cells or animals, M. Schlesinger et al., Cold Spring Harbor Laboratory, 1982; M. Pardue et al., Alan R.
Liss, Inc. (1989). In contrast, atherosclerotic plaques ;represent a system of chronic, multiple stresses. To more closely parallel these conditions, and especially those found in the necrotic core of a plaque, the present studies stressed cells by a combination of enzymatic cell release, hypoxia, low amino acid levels, and longer incubation periods.
Statistical differences were not cbserved in the test responses between normal and diseased arterial cell isolates. This may reflect the limited population size of this study, and/or the limited extent of atherosclerosis, i.e., the lack of arterionecrosis in these animals. Additionally, the procedure employed for cell release and the test conditions applied in this study may have caused a maximal hsp response for both normal and diseased cell isolates, masking differences in hsp responses present ln vivo. The large proportion of normal smooth muscle cells found in even the most diseased aortas might also have a masking effect. The lack of differences could a}so reflect the potential point of action for exogenous hsp. I hsp affects viability via plasmalemma effector sites whose composition or number do not change during atherogenesis, the reaction cells to exogenous hsp would be the same regardless of their level of lipid loadO Thus; the : ' ~ ' ' ' .
! . ~ ' ." ' ' . ,;' ' . ' ' ' .
! ,;' 2 ~ 7 ~
~ ~ results given here indicate a possible common pathway for the effect of exogenous hsp on arterial cells.
Viability and lysosomal membrane integrity are well correlated normally over a range o~ temperatures (Fig. l), but have discordant responses to exogenous hsp70. The positive effect of added hsp70 on viability of cell isolates was initiated by as little as 10 ng/103 cells and, once a significant effect was obtained, a ten fold increase in hsp concentration failed to induce further changes in cell viability (Fig. 3). This increase occurred over a range of temperatures, but was most significant at 37C (Fig. 4~, possibly due to a maximal activation of degradative enzymes in the cells under study at this temperature.
In contrast to cellular viability, lysosomal membrane integrity was not significantly changed by exogenous hsp70 (Fig. 5-). This observation may reflect a time-dependent factor yet to be determined. Figure 5 indicates that a decline in structure-linked lysosomal latency with temperature occurred for samples both with and without added hsp. If lysosomal NABA latency is an earlier marker than viability ~or membrane integrity in this system, measurements at time points before 20 hours may reveal changes in latency across all temperatures which are comparable to later changes in viability. To address this, time response studies are currently underway. Alternately, hsp70 may affect cell viability by a mechanism more specific than general cell membrane stabilization. If so, structure-linked lysosomal latency may be affected independently of viability or be unaf~ected by exogenous hsps.
E~UUMP~E 2 Prote~tion of Nerve ~is~ue ~lth H~P70 This experime~t was conducted to demonstrate the use of hsp70 to protect nerve tissue against damage using light damage in the rat retina as a model system.
Procedures were essentially as described in M. Barbe et ' .
. ~
~ ~ al., Science 241, 1817 (1988). hsp70 was as described ln connection with Example 1 above.
TWQ groups of three rats each received an in~ection into the vitreous chamber of the right eye of a saline solution that contained either 2 ~g or 10 ~g of purified hsp70. These rats al~o received in the left eye an injection of the saline solution alone to control for any effect the injection itself might have. A third group of two rats were not injected and served as untreated controls. A11 three groups were exposed to 175-200 foot-candles of fluorescent light beginning four hours after the injections and continuing for 24 hoursO
Two weeks after the light exposure, the eyes of each rat were prepared ~or routine histology and the nw~er o~
surviving photoreceptors in each eye determined by standard techniques. The difference in surviving photoreceptors between the right and left retinas was then calculated. A protective effect of the injected hsp70 is indicated when that difference is significantly greater than zero. On the other hand, if there was no effect of the injected hsp70, the loss of photoreceptors from the right and left eyes should average out to the same, giving a right-left difference that is not significantly different from zero.
Results are summarized in Figure 6. Based on a number of statistical comparisons, the group that received the 10 ug dose of Hsp70 showed significant protection of the retinal photoreceptors against the light damage (p~.05), with the right eye having about 36%
more photoreceptors than the }eft eye. The group that received the 2 ug dose of Hsp70 showed a trend in the same direction as the higher dose group, but it did not attain statistical significance with the small number of subjects tested.
The foregoing examples are illustrative of the present invention, and are not to be construed as limiting thereof. The in~ention is defined hy the 2~798~L3 --23~
:
~following claims, with equivalents of the claims to be in ::luded therein .
, .
''' .,~ .
, ; , ~` ` ' . ' '
Claims (28)
1. A method of combating mortality in a cell under stress, comprising contacting hsp70 to the cell in an amount effective to enhance the survival of that cell.
2. A method according to claim 1, wherein said hsp70 is animal hsp70.
3. A method according to claim 1, wherein said hsp70 is plant hsp70.
4. A method according to claim 1, wherein said hsp70 is bacterial hsp70.
5. A method according to claim 1, wherein said hsp70 is mammalian hsp70.
6. A method according to claim 1, wherein said cell is a plant cell.
7. A method according to claim 1, wherein said cell is an animal cell.
8. A method according to claim 1, wherein said cell is a bacterial cell.
9. A method according to claim 1, wherein said cell is a mammalian cell.
10. A method according to claim 1, wherein said cell is an arterial cell.
11. A method according to claim 1, wherein said cell is a nerve cell.
12. A method according to claim 1, wherein said cell is maintained in vitro and said contacting step is carried out in vitro.
13. A method of combating mortality in a tissue under stress, comprising contacting hsp70 to the tissue in an amount effective to enhance the survival of cells residing in that tissue.
14. A method according to claim 13, wherein said hsp70 is animal hsp70.
15. A method according to claim 13, wherein said hsp70 is mammalian hsp70.
16. A method according to claim 13, wherein said tissue is mammalian tissue.
17. A method according to claim 13, wherein said tissue is arterial tissue.
18. A method according to claim 13, wherein said tissue is nerve tissue.
19. A method according to claim 13, wherein said tissue is maintained in vitro and said contacting step is carried out in vitro.
20. A method of combating atherosclerosis in a human or animal subject in need of such treatment, comprising administering the subject hsp70 in an amount effective to reduce necrosis in arterial plaques residing in the subject.
21. A method according to claim 20, wherein said administering step is carried out by intravenous injection.
22. A method of combating arterial restenosis after angioplasty in a human or animal subject in need of such treatment, comprising administering arterial tissue residing in the subject in need of such treatment hsp70 in a restenosis-combating amount.
23. A method of combating nerve damage in a human or animal subject in need of such treatment, comprising administering the subject hsp70 in an amount effective to enhance the survival of nerve cells under stress.
24. A method according to claim 24, wherein said stress is anoxic stress.
25. A method according to claim 24, wherein said stress is anoxic stress arising from a stroke.
26. A pharmaceutical composition comprising a therapeutically effective amount of hsp70 in a pharmaceutically acceptable formulation.
27. A pharmaceutical composition according to claim 26, wherein said hsp70 is animal hsp70.
28. A pharmaceutical composition according to claim 27, wherein said hsp70 is mammalian hsp70.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50593490A | 1990-04-06 | 1990-04-06 | |
| US505,934 | 1990-04-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2079813A1 true CA2079813A1 (en) | 1991-10-07 |
Family
ID=24012485
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002079813A Abandoned CA2079813A1 (en) | 1990-04-06 | 1991-04-05 | Method of treatment with hsp70 |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0527783A4 (en) |
| JP (1) | JPH05507908A (en) |
| AU (1) | AU659085B2 (en) |
| CA (1) | CA2079813A1 (en) |
| WO (1) | WO1991015219A1 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5811447A (en) * | 1993-01-28 | 1998-09-22 | Neorx Corporation | Therapeutic inhibitor of vascular smooth muscle cells |
| US5847007A (en) * | 1993-05-13 | 1998-12-08 | Neorx Corporation | Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells |
| EP1066050B2 (en) † | 1998-03-27 | 2010-06-02 | Gabriele Prof. Dr. Multhoff | Application of hsp70 proteins |
| US6812205B2 (en) * | 2000-03-15 | 2004-11-02 | The Brigham & Women's Hospital, Inc. | Suppression of vascular disorders by mucosal administration of heat shock protein peptides |
| EP1523323B1 (en) | 2001-08-23 | 2013-07-24 | Arizona Board Of Regents | Reagents and methods for smooth muscle therapies |
| EP1531160B1 (en) * | 2003-11-12 | 2010-12-29 | Alfa Biogene International B.V. | Recovery of a heat shock protein |
| CN101801402B (en) | 2007-07-06 | 2013-08-28 | 乌得勒支大学控股有限公司 | Treatment and prevention of inflammatory diseases and autoimmune diseases |
-
1991
- 1991-04-05 CA CA002079813A patent/CA2079813A1/en not_active Abandoned
- 1991-04-05 JP JP91507657A patent/JPH05507908A/en active Pending
- 1991-04-05 AU AU76773/91A patent/AU659085B2/en not_active Ceased
- 1991-04-05 EP EP19910908050 patent/EP0527783A4/en not_active Withdrawn
- 1991-04-05 WO PCT/US1991/002363 patent/WO1991015219A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU659085B2 (en) | 1995-05-11 |
| JPH05507908A (en) | 1993-11-11 |
| AU7677391A (en) | 1991-10-30 |
| EP0527783A1 (en) | 1993-02-24 |
| EP0527783A4 (en) | 1993-09-01 |
| WO1991015219A1 (en) | 1991-10-17 |
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