Evaluation of Cutaneous Irritancy Using Human Skin Recombinants.
- Author:
Bang Soon KIM
1
;
Dong Youn LEE
;
Ji Hyun HAN
;
Jong Hee LEE
;
Kwang Hyun CHO
Author Information
1. Department of Dermatology, Seoul National University College of Medicine, Korea. khcho@snu.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
Cutaneous irritancy;
Keratinocyte;
Human skin recombinant
- MeSH:
Animals;
Cell Culture Techniques;
Collagen;
Dermis;
Epidermis;
Healthy Volunteers;
Humans*;
Interleukin-1alpha;
Irritants;
Keratinocytes;
Mass Screening;
Neutral Red;
Organ Culture Techniques;
Patch Tests;
Polyethylene;
Skin*
- From:Korean Journal of Dermatology
2002;40(12):1505-1517
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: There is an increasing need for the development of in vitro models capable of substituting for animals in cutaneous irritancy studies. Until now, various culture models have been developed, including skin organ cultures, conventional and air-exposed cell cultures. The air-exposed culture forms a multilayered epidermis showing an overall structure which resembles that of a native epidermis. The presence of a coherent stratum corneum layer in these cultures permits the application of potential irritants at the concentrations and formulations which are applied in vivo. Recently, a new human skin recombinant, made of human keratinocytes cultured on de-epidermized dermis with fibroblast-populated collagen matrix, has been developed and appears to represent a better skin equivalent model than previous models. OBJECTIVE: In the present study, monolayer-cultured human keratinocytes and the new human skin recombinants were evaluated for the test models of various skin irritants. METHODS: The extent of skin irritancy induced after application of 3 different irritants (sodium lauryl sulfate, methyl paraben, and polyethylene glycol-400) was evaluated on the basis of (1) MTT assay, (2) neutral red uptake assay, (3) LDH release, and (4) release of IL-1 alpha. In the human skin recombinants, morphological perturbations and changes in the expression of differentiation-specific protein markers (keratin 1, involucrin, filaggrin, and loricrin) were also evaluated. To determine the difference between in vivo and in vitro models for the detection of irritancy, a patch test was performed on 11 normal human volunteers with various concentrations of the different irritants RESULTS: The results of the present study show that irritant cytotoxicity correlates well with irritant concentration in both monolayer-cultured human keratinocytes and the new human skin recombinant. The new human skin recombinant is superior to monolayer culture as an in vitro model for skin irritancy screening in that the concentrations of test irritants are the same as in vivo. With the human skin recombinant, morphological changes were observed according to the irritant concentration. CONCLUSION: The new human skin recombinant can be used as an alternative to animals for skin irritancy screening.
