Brod J, Bavelier E, Justine P, Weerheim A, Ponec M
Department of Biology, L'Oréal Research Laboratories, Aulnay ss Bois, France.
In Vitro Cell Dev Biol. 1991 Feb;27A(2):163-8. doi: 10.1007/BF02631004.
Epidermal differentiation is accompanied by profound changes in the synthesis of a variety of intracellular proteins and intercellular lipids. In conventional, submerged culture keratinocytes have been shown to lose the ability to synthesize the protein markers of differentiation. They re-express them, however, when they are cultured in medium supplemented with delipidized [retinoic acid (RA)-depleted] serum or in air-exposed cultures using de-epidermized dermis (DED) as a substrate. Recent studies have revealed that acylceramides (AC) and lanosterol (LAN), which are present only in trace amounts in cultures of keratinocytes grown under submerged conditions on DED in medium supplemented with normal serum, become expressed in significant amounts when the culture is lifted to the air-liquid interface. Inasmuch as culture conditions may markedly affect the extent of keratinocyte differentiation, the present study aimed to investigate the effect of normal (RA-containing) or delipidized (RA-depleted) serum and of RA administration on lipid composition (especially of the AC and LAN contents) in cells cultured under submerged and air-exposed conditions. To test a possible effect of dermal substrate (used in the air-exposed model), the lipid composition of keratinocytes grown under submerged conditions on a plastic and on a dermal substrate (de-epidermized dermis, DED) has also been compared. The results revealed that under all culture conditions, RA deprivation of fetal bovine serum resulted in a marked increase of total ceramide content. Even under submerged conditions, the presence of both AC and LAN could be detected. In air-exposed culture, the content of these lipids was markedly increased. Addition of RA at 1 microM concentration to cultures grown in RA-depleted medium induced marked changes in lipid composition under all culture conditions tested. In cells grown under submerged conditions (both on plastic and on DED) AC and LAN were no longer present in detectable amounts. Also in air-exposed culture, a marked decrease in the content of these lipids was observed. These results suggest that liposoluble serum components, like RA, control the synthesis of lipids that are present in later stages of epidermal differentiation.
表皮分化伴随着多种细胞内蛋白质和细胞间脂质合成的深刻变化。在传统的浸没培养中,角质形成细胞已被证明会丧失合成分化蛋白标志物的能力。然而,当它们在补充有脱脂(不含视黄酸(RA))血清的培养基中培养或在使用去表皮真皮(DED)作为底物的暴露于空气中的培养物中培养时,它们会重新表达这些标志物。最近的研究表明,酰基神经酰胺(AC)和羊毛甾醇(LAN),在补充有正常血清的DED上于浸没条件下生长的角质形成细胞培养物中仅以痕量存在,当培养物升至气液界面时会大量表达。由于培养条件可能会显著影响角质形成细胞的分化程度,本研究旨在探讨正常(含RA)或脱脂(不含RA)血清以及RA给药对在浸没和暴露于空气中的条件下培养的细胞中脂质组成(特别是AC和LAN含量)的影响。为了测试真皮底物(用于暴露于空气中的模型)的可能作用,还比较了在塑料和真皮底物(去表皮真皮,DED)上于浸没条件下生长的角质形成细胞的脂质组成。结果显示,在所有培养条件下,胎牛血清的RA缺失导致总神经酰胺含量显著增加。即使在浸没条件下,也能检测到AC和LAN的存在。在暴露于空气中的培养物中,这些脂质的含量显著增加。在不含RA的培养基中生长的培养物中添加1 microM浓度的RA,在所有测试的培养条件下均诱导脂质组成发生显著变化。在浸没条件下生长的细胞(无论是在塑料上还是在DED上)中,AC和LAN不再以可检测的量存在。同样在暴露于空气中的培养物中,观察到这些脂质的含量显著降低。这些结果表明,脂溶性血清成分,如RA,控制着表皮分化后期存在的脂质的合成。