WO1993013204A2 - Mittel zur stimulierung der teilungsaktivität tierischer zellen - Google Patents
Mittel zur stimulierung der teilungsaktivität tierischer zellen Download PDFInfo
- Publication number
- WO1993013204A2 WO1993013204A2 PCT/EP1992/002929 EP9202929W WO9313204A2 WO 1993013204 A2 WO1993013204 A2 WO 1993013204A2 EP 9202929 W EP9202929 W EP 9202929W WO 9313204 A2 WO9313204 A2 WO 9313204A2
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- WO
- WIPO (PCT)
- Prior art keywords
- cells
- gene
- recombinant
- sequence
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
- C12N15/1135—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against oncogenes or tumor suppressor genes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4702—Regulators; Modulating activity
- C07K14/4705—Regulators; Modulating activity stimulating, promoting or activating activity
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4746—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used p53
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/82—Translation products from oncogenes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/31—Chemical structure of the backbone
- C12N2310/315—Phosphorothioates
Definitions
- the invention relates to a means for stimulating the
- Immortal cell lines can either be obtained directly from certain tumors or can be derived from primary cells that have been isolated from certain tissues.
- the spontaneous emergence of an immortal cell line is an extremely rare event, since at least two mutations are probably required for this.
- tumor viruses have therefore often been used as inducers of immortalization.
- these had the disadvantage that they also caused a frequently undesirable tumorigenic change in the cells.
- DD-WP 265165 it has already been proposed to use the recombinants with the gene for the large T antigen of the polyomavirus to improve the immortalization process. In principle, this solved the problem of effective immortalization without simultaneous tumorigenic changes.
- the speed of cell division is usually not affected by this method.
- REPLACEMENT LEAF Many animal and human cells have a dividing potential limited to approx. 50-60 cell divisions without immortalization.
- the aim of the invention is to create and use an agent for the general stimulation of the division activity of animal and human cells in culture, both with regard to the utilization of the natural division potential and with regard to the speed of the cell cycle.
- the agent according to the invention is characterized in that it contains as active substance one or more nucleotide sequences with a complementary sequence (antisense) to certain areas of the mRNA of tumor suppressor genes or other genes which have a negative effect on cell division activity.
- the antisense nucleotide sequence preferably consists of a synthetic oligonucleotide with a length of at least 15 nucleotides, a length of 18-21 nucleotides being preferred.
- the oligonucleotide must be in a nuclease resistant form, with the phosphothioate form being particularly useful.
- Sequences which are complementary to a region of the 5 ′ end, the region around the start codon, a region of an exon or a region at an intron-exon junction of the gene in question are primarily used as antisense nucleotide sequences.
- Complementary sequences to the tumor suppressor gene retinoblastoma gene, p53 gene or the E-cadherin are preferably selected.
- Examples of specific sequences of the active substance in the agent according to the invention are 3'-CAGTACGGCGGGTTTTGG-5 'and 3'-AGCAAGTGAAAATGACTC-5'.
- Oligonucleotides sterilized by alcohol precipitation, in sterile dist. Dissolved water and added in a concentration of 5 - 30 M in the culture medium without serum. The oligonucleotides can also be mixed with lipofectin in order to achieve an even more effective uptake by the cells. The cells are incubated with the oligonucleotide-containing medium for several days. The number of cells is checked daily in parallel batches
- HEL primary human lung fibroblasts
- Oligonucleotides for at least 7 days Within 10 days, at least 3 times the number of cells becomes with this cell type
- Pairing with the antisense oligonucleotide is degraded.
- the immunological protein detection shows that at the latest 3 days after the start of the treatment with oligonucleotides
- the treated culture is left in the confluent for more than 7 days
- the agent according to the invention makes it possible to significantly increase the number of cell divisions per unit time. Its application also enables the cultivation of cells that cannot otherwise be cultivated. This enables great progress in both biotechnological substance production and in basic biological medical research.
- a further embodiment of the invention consists in not adding the antisense nucleotide sequence to stimulate cell growth, but in generating it in the cell to be cultivated. This is achieved in that a recombinant with an expressible antisense sequence is introduced into the cells by transfection.
- the preferred sequence consists of 50-500 nucleotides.
- the recombinant according to the invention contains the antisense nucleotide sequence in the reading direction after a strong promoter.
- the sequence preferably consists of complementary sequences of the tumor suppressor gene retinoblastoma gene, p53 gene or E-cadherin.
- a particularly suitable sequence consists of the first 360 nucleotides of the mRNA coding sequence of the retinoblastoma gene.
- the T7 promoter in combination with its homologous RNA polymerase is particularly suitable as a promoter for the recombinant.
- a recombinant is produced, a selected sequence, preferably 50-500 nucleotides long, being cloned from the relevant tumor suppressor gene in antisense orientation behind a strong promoter.
- This recombinant is preferably transfected into the relevant cells together with a selection marker and the gene of T7 RNA polymerase according to methods known per se. After selection for the presence of the marker (e.g. pac), cells are obtained whose division activity is clearly stimulated.
- the marker e.g. pac
- oligonucleotide with the sequence 3'-rCAGTACGGCGGGTTTTGG-5 ' is synthesized as a phosphothioate by a known method on an automatic synthesizer (Applied Biosystems) and dried.
- Approximately 100 OD units are dissolved in 100 l of H 2 O, adjusted to 0.3 M Na acetate and precipitated with 10 volumes of 96% ethanol at -70 ° C.
- the precipitate is centrifuged off and dissolved in 0.5 ml of sterile water. After measuring the concentration, dilute to 1 ⁇ * -q / ⁇ by adding water.
- This solution is diluted 60 ⁇ in 1 ml of cell culture medium, which corresponds to a concentration of 10 ⁇ cM. This solution is applied to the cells previously sown in a 5 cm culture dish.
- Cells used at a density of 5 x 10 cells per dish There are 8 dishes with oligonucleotide and without (control). After one hour, 1 ml of medium with 10% serum is added. The following day, the cells are harvested from a dish and counted in a counting chamber. The results are shown graphically (see Figure 2) and show a much faster increase in the number of cells from the 2nd to the 10th day. After 10 days, a subculture is created, which is treated again with oligonucleotide in the manner described above. The renewed daily cell count results in basically the same curve, whereby the difference after the 1st and 2nd day is more clearly recognizable than in the first round.
- An oligonucleotide with the sequence 3'-AGCAAGTGAAAATGACTC-5 ' is prepared as described under 1, prepared for use and added to the cell culture.
- the inclusion of a growth curve by daily cell counting results in principle in the same curve as in Figure 2, but after 10 days there are not 3.5 times, but only 2.5 times more cells.
- the oligonucleotides of Examples 1 and 2 are used in combination in a concentration of 5 M each, and the cell number is determined daily. This results in a steeper curve increase with a multiple of the number of cells compared to the control cells after 10 days.
- Example 4
- the gene of the T7 RNA polymerase modified by a nuclear localization signal with the poly (A) signal of the thymidine kinase gene was obtained as a BglII / PvuII fragment (3267 bp) from pMTT7N (Lieber et al. (1989) Nucl.Acids Res 17: 8485-8493) and inserted into the retroviral vector pM6pac.
- the gene of T7 RNA polymerase is under the control of the "early" SV40 promoter. Cell clones expressing this recombinant can be selected with puromycin.
- the plasmid can be packaged in a retrovirus. From several tested restriction fragments of the cDNA of the human retinoblastoma (Rb) gene a 360 bp fragment (Hpal / Asp718) was found, which encompasses the 5'-untranslated region and the l. Exon of the Rb gene covers, as suitable for cell division stimulation by means of anitsense Rb RNA expression. This fragment was cloned into the pBluescript KS vector cut with Asp718 / EcoRI and treated with phosphatase by ligation of the cohesive Asp718 ends and subsequent filling in of the 5 'protruding Hpal and EcoRI ends with Klenow polymerase and ring closure. A recombinant was selected by sequencing with T7 primer which contains the fragment of the Rb gene in the antisense (3 '5') direction behind the T7 promoter
- T7asRbl Modified T7 RNA polymerase coexpressed in mammalian cells highly efficiently transcribes (? 25000 RNA molecules / cell) a gene under the T7 promoter (Lieber et al. (1993) Methods Enzymol. Vol. 217, in press). Both plasmids were cleaned using a CsCl gradient.
- NIH 3T3 cells embryonic cells
- 225 __l ⁇ are in a 15 ml Falcon tube. 2 .0 with S / * q pT7asRbl and 2 9 pM6SVT7N presented. 25 / ⁇ . 2.5 M CaCl 2 . are added and with vortex mixing 250 ⁇ -1 2xHBS buffer pH 6.96 in the DNA
- antisense RNA which is generated by a human Rb gene in mouse cells, has an expression-inhibiting effect.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Toxicology (AREA)
- Oncology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- Physics & Mathematics (AREA)
- Plant Pathology (AREA)
- Microbiology (AREA)
- Cell Biology (AREA)
- Immunology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/511,836 US5831067A (en) | 1991-12-18 | 1995-08-07 | Agent for stimulating animal cell division |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP4142452.2 | 1991-12-18 | ||
DE19914142452 DE4142452A1 (de) | 1991-12-18 | 1991-12-18 | Mittel zur stimulierung der teilungsaktivitaet tierischer zellen |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1993013204A2 true WO1993013204A2 (de) | 1993-07-08 |
WO1993013204A3 WO1993013204A3 (de) | 1993-08-05 |
Family
ID=6447798
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1992/002929 WO1993013204A2 (de) | 1991-12-18 | 1992-12-17 | Mittel zur stimulierung der teilungsaktivität tierischer zellen |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0572641A1 (de) |
DE (1) | DE4142452A1 (de) |
WO (1) | WO1993013204A2 (de) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5759776A (en) * | 1995-06-05 | 1998-06-02 | California Pacific Medical Center | Targets for breast cancer diagnosis and treatment |
US5776683A (en) * | 1996-07-11 | 1998-07-07 | California Pacific Medical Center | Methods for identifying genes amplified in cancer cells |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5830723A (en) * | 1996-08-13 | 1998-11-03 | Regents Of The University Of Minnesota | Method for immortalizing chicken cells |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990009180A1 (en) * | 1989-02-15 | 1990-08-23 | Board Of Regents, The University Of Texas System | Methods and compositions for treatment of cancer using oligonucleotides |
WO1992005272A1 (en) * | 1990-09-17 | 1992-04-02 | The Regents Of The University Of California | Method and composition for controlling proliferation of cells |
-
1991
- 1991-12-18 DE DE19914142452 patent/DE4142452A1/de not_active Withdrawn
-
1992
- 1992-12-17 EP EP19930902113 patent/EP0572641A1/de not_active Withdrawn
- 1992-12-17 WO PCT/EP1992/002929 patent/WO1993013204A2/de not_active Application Discontinuation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990009180A1 (en) * | 1989-02-15 | 1990-08-23 | Board Of Regents, The University Of Texas System | Methods and compositions for treatment of cancer using oligonucleotides |
WO1992005272A1 (en) * | 1990-09-17 | 1992-04-02 | The Regents Of The University Of California | Method and composition for controlling proliferation of cells |
Non-Patent Citations (4)
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5759776A (en) * | 1995-06-05 | 1998-06-02 | California Pacific Medical Center | Targets for breast cancer diagnosis and treatment |
US5776683A (en) * | 1996-07-11 | 1998-07-07 | California Pacific Medical Center | Methods for identifying genes amplified in cancer cells |
Also Published As
Publication number | Publication date |
---|---|
EP0572641A1 (de) | 1993-12-08 |
WO1993013204A3 (de) | 1993-08-05 |
DE4142452A1 (de) | 1993-06-24 |
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