KR101770983B1

KR101770983B1 - Manufacturing method of 3D human skin model and method for estimating Human toxicoid chemicals using the same

Info

Publication number: KR101770983B1
Application number: KR1020150108415A
Authority: KR
Inventors: 이수현; 정행선; 김설영; 김혜수; 조선영
Original assignee: 주식회사 바이오솔루션
Priority date: 2015-07-31
Filing date: 2015-07-31
Publication date: 2017-08-25
Also published as: KR20170014678A

Abstract

TECHNICAL FIELD The present invention relates to a method for producing a three-dimensional artificial skin model using low temperature culture and a method for evaluating a human toxic substance using the same. More specifically, The present invention relates to a method for producing an artificial skin model for evaluating a human toxic substance and a method for evaluating a human toxic substance using the same at a temperature of 31 to 33 DEG C after air-liquid culture at 37 DEG C during the dimensional culture .
According to the present invention, when an artificial skin model is prepared by culturing at a low temperature, the artificial skin cells are promoted to differentiate and migrate and the stratum corneum formation of the artificial skin is promoted to provide a more stable artificial skin model. In the toxic substance test or skin irritation test It can improve problems such as false positives and provide high reproducibility.

Description

TECHNICAL FIELD The present invention relates to a method for manufacturing a three-dimensional artificial skin model using low temperature culture and a method for evaluating human toxic substances using the same.

TECHNICAL FIELD The present invention relates to a method for producing a three-dimensional artificial skin model using low temperature culture and a method for evaluating a human toxic substance using the same. More specifically, The present invention relates to a method for manufacturing an artificial skin model for evaluating human toxic substances and culturing the same at a temperature of 31 to 33 ° C after air-liquid culture at 37 ° C during dimensional culture, and a method for evaluating human toxic substances using the same .

The skin of the human body is the largest organ among the organs it carries, and protects the human body by forming a protective film to prevent moisture and heat from being taken out of the body. Skin is not only used as a means of communicating information with the outside, but also plays an important role in controlling the body temperature by releasing sweat, and sometimes also serving as an aesthetic reference. If the main function of the keratinocytes constituting the epidermis is to protect the human body from external contaminants or stimuli by forming a skin barrier by combining keratin protein and lipid, melanin cells, another constituent cell of the epidermis, synthesize melanin, It transmits ultraviolet rays on the nucleus of cells to protect the genetic information of human body by blocking harmful ultraviolet rays.

Since the skin of the human body is exposed directly to the outside, it is a part of the body which is susceptible to damage by chemicals or irritants. Contact with chemicals or irritants may cause skin damage. In addition, since many chemicals are currently in use and new chemicals are constantly being developed, toxicity testing of human skin must be performed correctly before using these chemicals.

In the conventional laboratory-based toxicity test method, the keratinocytes or fibroblasts constituting the epidermis of the human skin were cultured in a single culture medium, and then the culture medium was treated with chemicals, and MTT reduction test, NRU test, Alamar Blue test, Kenacid Blue The toxicity was measured by the test method and the LDH test method. However, when the single layer culture of keratinocytes is carried out while the keratinocytes are submerged in a culture medium, most of the cultured cells have the property of cells corresponding to the basal layer of the epidermis It does not reflect the characteristics of the human epidermis, and since the outermost layer of the epidermis is not formed, the toxicity of the stratum corneum which is first contacted when the chemical substance comes into contact with the human skin can not be accurately determined.

Therefore, many laboratory animals are used to clearly evaluate the toxicity results of chemicals. However, in recent years, regulations on animal testing have been strengthened in order to protect experimental animals by strengthening bioethics and 3R principles (Reduction, Replacement, Refinement) for animal experiments in various countries. (Botham, 2004; Fentem, 2001; Kimber, 1999).

Epiderm used in skin irritation substitution test in foreign countries is developed by MatTek (USA). Epidermal keratinocytes (NHEK) obtained from normal human body are cultured in Millicell cell culture insert to obtain multi-layered, differentiated in vitro human epidermis . Episkin consists of a type IV human collagen layer on the type I, III collagen layer corresponding to Dermis developed by Episkin-SNC (france), and an epidermis layer composed of human keratinocyte on it (ECVAM, 2007a, 2007b).

Generally, the artificial skin model is prepared by culturing keratinocytes in the human body at 37 ° C in a three-dimensional manner and using them for experiments. As described above, the test using the artificial skin model has advantages in solving the solubility problem and resembling human skin, and thus it has been utilized in alternative test methods for skin corrosion test and skin irritation test.

However, the artificial skin model made by the above-mentioned method has a poor false-natured error in the skin stimulation test when the stratum corneum is formed in comparison with the stratum corneum of normal skin. In other words, there is a problem that toxic substances which should appear as negative in general are positive in artificial skin in which stratum corneum is poorly formed, so that evaluation of toxic substances can not be accurately performed.

In order to overcome the problems of the prior arts, the inventors of the present invention have conducted intensive studies and have found that, in order to produce an artificial skin model by three-dimensionally culturing keratinocytes isolated from a human body, the present invention provides a more stable artificial skin model by promoting the differentiation and migration of artificial skin cells and the stratum corneum formation of artificial skin when the artificial skin model is cultured at an additional temperature of 31 to 33 ° C after air-liquid culture, Toxic substance test or skin irritation test, it is possible to improve problems such as false positives and to provide high reproducibility. Thus, the present invention has been completed.

Accordingly, it is a main object of the present invention to provide a more stable artificial skin model by promoting differentiation and migration of artificial skin cells and stratum corneum formation of artificial skin, thereby improving problems such as false positives in toxic substance test or skin irritation test And a method for manufacturing a three-dimensional artificial skin model using low-temperature culture with high reproducibility.

It is another object of the present invention to provide a method for testing skin irritation of a human toxic substance using an artificial skin model manufactured using the above-mentioned low temperature culture.

According to one aspect of the present invention, there is provided a method for producing an artificial skin model by three-dimensionally culturing keratinocytes isolated from a human body, comprising the steps of: (a) adding an air-liquid culture at 37 ° C in a three- And culturing the cells at low temperature at 31 to 33 占 폚.

Conventionally, artificial skin models made by culturing the keratinocytes three-dimensionally at 37 占 폚 have a problem in that the stratum corneum is poorly formed and the false-positive errors frequently appear in the skin stimulation test. Accordingly, the present inventors confirmed that when the artificial skin model is manufactured using the low-temperature culture, the artificial skin model can be provided by promoting the differentiation and migration of artificial skin cells and the stratum corneum formation of the artificial skin, .

The present invention provides a method for manufacturing an artificial skin model for evaluating human toxicity, comprising the steps of:

a) separating keratinocytes from human skin tissue and subculturing the keratinocytes;

b) placing the keratinocytes in a culture insert;

c) culturing the culture insert in a submerged state covered with a culture medium at 37 캜 to allow the epithelial cells to grow evenly;

d) culturing the epithelial cell layer at 37 ° C in an air-liquid culture method for exposing the epithelial cell layer to air; And

e) further culturing the gas-liquid culture at a temperature of 31 to 33 ° C to induce differentiation.

More specifically, in step b), the keratinocytes are preferably inoculated at 1 × 10 ⁵ cells / 200 μl. In the step c), the submerged state is cultured for 4 to 7 days to allow the epithelial cells to grow evenly. In the gas-liquid culture method in the step d), induction of differentiation into cells in a so-called air- . It is preferable that the gas-liquid culture method is performed for 12 to 16 days, at which time the medium is replaced every 2 to 3 days. It is preferable that all the cultivation is performed at 37 캜.

The conventional culture method is performed at 37 DEG C as described above, but the present invention is characterized in that a low temperature culture is performed at 31 to 33 DEG C for 3 days after the culturing method is added. The low-temperature incubation temperature is 31 to 33 ° C, preferably 32 ° C.

In the present invention, the production method promotes differentiation and migration of artificial skin cells.

In the present invention, the production method promotes the formation of stratum corneum of the artificial skin.

According to the experimental example of the present invention, it was confirmed that the artificial skin model prepared by the culture method of the present invention promoted stratum corneum formation more than artificial skin model prepared by the conventional culture method. From these results, it can be said that the artificial skin model manufacturing method of the present invention promotes the differentiation and migration of the cells and the formation of the stratum corneum, thereby contributing to the stabilization of artificial skin model production (see Example 2, Fig. 1) .

In the present invention, the artificial skin model is characterized in that a false-positive error is improved in a skin irritation test.

The evaluation of the irritation to the human skin is based on scoring the erythema of erythema using an experimental rabbit to evaluate the irritability. The OECD Guideline (OECD Test Guideline 439) provides guidance on the toxicity assessment of human skin irritation tests using artificial skin, and includes a list of stimulant, non-stimulating reference materials and toxicity assessment criteria , Less than 50 stimuli) is specified.

According to the experimental example of the present invention, skin irritation test was conducted through naphthalene acetic acid, allyl phenoxy-acetate and isopropanol, which are non-magnetic substances of skin disclosed in OECD TG439. As a result, (Cell viability of 50% or less), but it was confirmed that the artificial skin produced by the culturing method of the present invention appeared to be negative (non-magnetic substance) (cell survival rate was 50% or more). These results indicate that the artificial skin prepared by the culturing method of the present invention can improve the false positive error of the skin toxic substance or the irritant substance in the skin stimulation test (see Example 3, FIG. 2).

According to another aspect of the present invention, the present invention provides a skin irritation test method for human toxicity substance comprising the following steps.

a) preparing an artificial skin model by three-dimensionally culturing keratinocytes according to claim 1;

b) treating the human toxicity candidate material with the artificial skin model;

c) measuring the survival rate of keratinocytes in the artificial skin model.

As described above, when an artificial skin model is manufactured by culturing at a low temperature, the artificial skin cells are promoted to differentiate and migrate and the stratum corneum formation of the artificial skin is promoted to provide a more stable artificial skin model. In the toxic substance test or skin irritation test Problems such as a false positive error can be solved.

Fig. 1 shows the results of an artificial skin model prepared by two culturing conditions (conventional culturing (all cultures at 37 ° C) and low temperature cultivation (culturing at 32 ° C for three days in a gas-liquid culture) with hematoxylin and eosin Fig.
FIG. 2 is a graph showing the results of a skin stimulation test using a human skin model prepared by a conventional culture method (all cultures at 37 ° C. for all periods) and a low-temperature culture method (culturing at 32 ° C. for 3 days of vapor-liquid culture) And graphs the results.

Hereinafter, the present invention will be described in more detail with reference to Examples. These embodiments are only for illustrating the present invention, and thus the scope of the present invention is not construed as being limited by these embodiments.

Example 1: Isolation and culture of keratinocytes

The resected skin tissue was washed more than 8 times with phosphate buffer (WelGENE) containing 50 μg / ml of antibiotic (gentamicin, Gibco) to remove the coagulated blood and contaminants. Subsequently, the fat layer of the dermis was removed, the tissue was cut as thin as possible to about 5 mm, the cut skin tissue was transferred to a 50 ml tube, and 10 ml of trypsin solution (0.125% trypsin: versene = 1: 1, Gibco) After the addition, physical stimulation was applied for 45 minutes at room temperature using a magnetic bar to allow the keratinocytes to come off. To the trypsin solution from which the cells were detached, 0.1 mg / ml trypsin inhibitor (Gibco) was added and transferred to a 50 ml tube. After centrifugation at 300 xg, supernatant was removed and KGM (Cambrex) And the cells were unified. The number of cells was calculated and divided into 1x10 ⁶ cells in a 100 mm diameter culture dish. The cells were cultured in a 37 ° C CO ₂ incubator and the medium was replaced once every 2 days. When the cells in the culture dish became overcooked, the keratinocyte culture medium of the culture dish was removed and washed once with phosphate buffer solution. Then, 2 ml of trypsin-EDTA solution was added, and the reaction was carried out in an incubator for 4 minutes. The keratinocytes were recovered from the culture vessel, and the number of cells was calculated and centrifuged at 300 xg. After removing the supernatant by centrifugation, the keratinocyte culture medium was added to suspend the keratinocytes in an even manner, and the cells were subcultured by adding a cell suspension to a 100 mm culture dish so as to have a cell count of 3 x 10 ⁵ cells.

Example 2: Three-dimensional culture of artificial skin and low temperature culture

The main factors leading to the differentiation of skin epithelial cells are calcium and air-dry. Three-dimensional culture is a three-dimensional culture method in which epidermal cells are inoculated and cultured to form highly differentiated human epidermal models of multiple layers. The epidermal cells are cultured in the middle of the air layer and the water layer, thereby differentiating into the middle layer squamous epithelium and keratinized. First, to obtain keratinocytes, keratinocytes cultured in a 100 mm dish were trypsinized, recovered from the culture dish, counted, and blunt-ended and cultured after inoculation with 1 x 10 ⁵ cells / 200 μl per millicell . For the culture of animal cells, a 3: 1 mixed medium of DMEM (Dulbecco's Modified Eagle's Medium) and Ham's F12 was used as a medium. This medium was supplemented with 10% fetal bovine serum (FBS), 5 μg / mL insulin, 5 μg / mL transferrin, 400 ng / mL hydrocortisone, 10-9 M cholera toxin, 10 μg / mL epithelial growth factor EGF), 10 units / mL penicillin and 10 mu g / mL streptomycin. After incubation for 5 days in a submerge state covered with the above-mentioned culture medium, the epithelial cells were allowed to grow evenly. The epithelial cells were air-liquid cultured by exposing the epithelial layer to air, Followed by further culturing to induce differentiation into a stratified layer. The badge exchange took place once every 2-3 days. Existing cultures are carried out at 37 ° C throughout the entire incubation period, and in this low temperature culture, they are transferred to an incubator at 32 ° C during the last 3 days of vapor-liquid incubation.

Figure 1 shows the histopathological differences between H & E staining and H & E staining to determine the difference between the conventional culture (37 ° C for all periods) and the low temperature culture (for 3 days, at 32 ° C). As shown in FIG. 1, it was confirmed that the formation of the stratum corneum during the low temperature culture was promoted.

Example 3: Skin irritation test using artificial skin

3-1: pre-culture

Add 0.9 ml per well to a 6-well plate of culture medium E-media kept warm in a water bath. Carefully transfer the prepared human skin model to each well while tilting the plate to prevent air bubbles from forming. Stabilize in a 5% CO ₂ incubator at 37 ° C for approximately 22 ± 2 hours.

3-2: Application of test substance

For the application of the test substance, the human skin model stabilized for 22 ± 2 hours in a 5% CO ₂ incubator at 37 ° C is taken out immediately before application of the substance. Use 6 well plates differently for each test substance. The test substance differs in the application method of the liquid and the solid depending on the characteristics. In the liquid, 30 μl of the test material is slowly dropped in the center of the human skin model, and the insert is returned and applied evenly, and covered with a nylon mesh to prevent air bubbles. Solids are prepared by measuring 30 mg of test substance in 1/4 size of herbage before application of test substance. When applying the test substance, first 30 μl of DPBS is dropped in the center of the skin model of the human body, and the insert is returned to spread evenly, and then 30 mg of the solid sample is applied thereon. It is possible to apply the test material to the surface of the human skin model by tapping the circle holding the insert. DPBS, which is a negative control substance used in the test, and allyl phenoxy-acetate, isopropanol, and naphthalene acetic acid, which are liquid samples, were tested according to the application method applicable to each property. After the test material is applied, cover the plate cover film in a 5% CO ₂ incubator at 37 ° C for 45 minutes to prevent evaporation or volatility.

3-3: Cleaning

The human skin model to which the test substance was applied at 37 ° C in a 5% CO ₂ incubator was taken out, and 10 ml of DPBS was divided into 4 ml of the inside of the insert to overflow the material and the nylon mesh, and if the nylon mesh did not fall off Remove with tweezers. After confirming that the nylon mesh has been removed, remove 10 ml of DPBS by overflowing 4 ml of the inside of the insert. Place the insert on sterile gauze to remove internal and external substances and DPBS. Place the insert in a 12-well plate and allow it to overflow with 4 ㎖ of DPBS at 10-second intervals. Stir for 1 minute and shake it. Finally, wash the inside and outside of the insert with 10 ml of DPBS slowly and divide 4 ml each time twice. After washing, remove the DPBS in and out of the insert using a 200 μl pipette, sterile gauze and a sterile cotton swab.

3-4: post-culture

Before entering the washing process, prepare a 6-well plate for the number of models beforehand and keep the culture liquid warm on the waterbath. Then, add 0.9 ml of culture medium per well to a prepared 6 well plate and warm it in a 5% CO ₂ incubator at 37 ° C. The washed human skin model is transferred to a 6-well plate containing 0.9 ml of culture medium per well and post-incubated for 42 ± 2 hours at 37 ° C in a 5% CO ₂ incubator.

3-5: Cell viability measurement (MTT measurement)

The MTT assay described below was used to assess the cell viability of the tissue during the test. MTT tissue survival analysis is a colorimetric assay system that measures the reduction of yellow methyl thiazolyl diphenyl-tetrazolium bromide (MTT) to an insoluble purple product by the mitochondria of living cells.

First, after the post-incubation, the inner and outer culture media of the human skin model are removed using a 200 μl pipette. Add 200 ㎕ of 0.3 ㎎ / ㎖ of MTT solution to a new 24 well plate, transfer the human skin model, and treat 100 ㎕ of MTT solution inside the human skin model. MTT-coated 24-well plates should be incubated for 3 hours in a shaker at 37 ° C and 5% CO ₂ incubator. After the application of MTT, remove foreign materials such as MTT inside and outside using a 200 ㎕ pipette. Next, transfer isopropanol to a new 6 well plate containing 1.9 ml / well, and then 100 μl of isopropanol is treated inside. Isopropanol-coated 6-well plates are shaded with aluminum foil, placed in a zipper bag and placed on a shaker for 3 hours to extract formazan. After Formazan extraction, add the extract to the inside of the human skin model with the external extract, and mix it by pipetting enough for the inmazan crystals in each well. 250 ㎕ per well is transferred into 96 well plate in 2 wells and the optical density (OD) is measured using a 96 well plate spectrophotometer (wavelength: 570 nm). The final value is the mean of two wells.

3-6: Determination of skin irritancy

The criteria for skin irritation are as follows. Based on this, it is judged whether the substance is irritating to the skin.

The cell viability of the negative control substance is determined as 100%, the cell viability is determined to be non-stimulating when the cell viability exceeds 50%, and the stimulus is determined to be 50% or less.

Prediction model Classification Mean tissue viability is ≤ 50% Irritant (I) R38 Mean tissue viability is> 50% Non-Irritant (NI)

Actually, naphthalene acetic acid, allyl phenoxy-acetate and isopropanol are known to be non-polar substances and should exhibit cell viability of 50% or more. FIG. 2 shows that the cytotoxicity of the toxic substance in the human skin model prepared by the conventional culture method was more than 50% due to the low temperature culture, and the human skin model was improved. It is confirmed that the formation of the stratum corneum is promoted through the low temperature culture method of the present invention, so that the shape of the stratum corneum is similar to that of the human skin, and at the same time, the skin irritation test is improved so as to enable accurate judgment of a substance exhibiting false- It can be concluded that the above method will contribute to high resilience and stabilization of model production.

As described above, according to the present invention, when an artificial skin model is manufactured by culturing at a low temperature, the present invention promotes the differentiation and migration of artificial skin cells and the stratum corneum formation of artificial skin to provide a more stable artificial skin model, By improving problems such as false positives in the test, high reproducibility can be provided.

Claims

In order to make an artificial skin model by three-dimensionally culturing the keratinocytes isolated from human body, it is characterized in that it is cultured at a temperature of 31 to 33 ° C at a low temperature after the air-liquid culture at 37 ° C in a three-dimensional culture A method for manufacturing an artificial skin model for evaluating human toxic substances.

2. The method of claim 1, wherein the artificial skin model for evaluating human toxicity substances comprises the steps of:
a) separating keratinocytes from human skin tissue and subculturing the keratinocytes;
b) placing the keratinocytes in a culture insert;
c) culturing the culture insert in a submerged state covered with a culture medium at 37 캜 to allow the epithelial cells to grow evenly;
d) culturing the epithelial cell layer at 37 ° C in an air-liquid culture method for exposing the epithelial cell layer to air; And
e) further culturing the gas-liquid culture at a temperature of 31 to 33 ° C to induce differentiation.

The method according to claim 1, wherein the method promotes differentiation and migration of artificial skin cells.

[2] The method of claim 1, wherein the method promotes the formation of a stratum corneum of an artificial skin.

The method of claim 1, wherein the artificial skin model is improved in false-positive error in a skin irritation test.

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