Regnier M, Darmon M
Cell Biology Department, Centre International de Recherches Dermatologiques, Valbonne, France.
In Vitro Cell Dev Biol. 1989 Nov;25(11):1000-8. doi: 10.1007/BF02624133.
It was possible to reconstruct epidermis in vitro by seeding dissociated keratinocytes on de-epidermized dermis and growing such recombined cultures for 1 wk, exposed to air, at the surface of the culture medium. These conditions were chosen to mimic the transdermal feeding and the exposure to the atmosphere that occur in vivo. Contrary to classical cultures performed on plastic dishes covered with culture medium, which show rudimentary differentiation and organization, the architecture of the stratified epithelium obtained in reconstructed cultures and the distribution of differentiation markers such as suprabasal keratins, involucrin, and membrane-bound transglutaminase were similar to those of the epidermis of skin biopsies; moreover, biochemical studies showed that the synthesis of the various keratins and the production of cornified envelopes was similar to what is found with skin specimens. The reconstructed epidermis model was found to be very useful to study in vitro the effect of retinoic acid on keratinocyte differentiation and epidermal morphogenesis.
通过将解离的角质形成细胞接种在去表皮的真皮上,并在培养基表面暴露于空气中培养这种重组培养物1周,可以在体外重建表皮。选择这些条件是为了模拟体内发生的经皮喂养和暴露于大气的情况。与在覆盖有培养基的塑料培养皿上进行的经典培养不同,经典培养显示出基本的分化和组织,而在重建培养物中获得的分层上皮结构以及分化标志物如基底上角质蛋白、内披蛋白和膜结合转谷氨酰胺酶的分布与皮肤活检表皮的结构相似;此外,生化研究表明,各种角质蛋白的合成和角质化包膜的产生与皮肤标本中的情况相似。发现重建的表皮模型对于在体外研究视黄酸对角质形成细胞分化和表皮形态发生的影响非常有用。