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皮肤中的从头甾醇生物合成。II. 由皮肤屏障需求调控。

De novo sterologenesis in the skin. II. Regulation by cutaneous barrier requirements.

作者信息

Menon G K, Feingold K R, Moser A H, Brown B E, Elias P M

出版信息

J Lipid Res. 1985 Apr;26(4):418-27.

PMID:4009060
Abstract

Recent studies suggest: that the epidermis and pilosebaceous epithelium are important sites of de novo sterol synthesis, and that the rate of cutaneous cholesterol synthesis does not change with alterations in circulating sterol levels. Since cutaneous sterols may be important for permeability barrier function, we studied the effect of experimentally altered barrier function on de novo sterologenesis in the epidermal and dermal layers of the skin. Epidermal sterologenesis appeared to be modulated by the skin's barrier requirements because topical detergent and acetone treatment stimulated de novo synthesis of nonsaponifiable lipids in the epidermis, but not in the dermis. Synthetic activity paralleled both the return of barrier function toward normal and the extent of prior damage to the barrier. Moreover, plastic-wrap occlusion of solvent-treated sites simultaneously corrected both the barrier abnormality and normalized sterol synthesis, further linking increased epidermal sterologenesis to barrier requirements. Whereas topical applications of a variety of other topical lipids did not down-regulate synthesis, epicutaneously applied 25-hydroxycholesterol appeared to diminish synthesis. These results suggest that maintenance of barrier function is one purpose of epidermal de novo nonsaponifiable lipid synthesis, and demonstrate further that, despite a lack of low density lipoprotein receptors, epidermis can regulate its lipid-synthetic apparatus in response to certain specific requirements.

摘要

近期研究表明

表皮和毛囊皮脂腺上皮是从头合成甾醇的重要部位,且皮肤胆固醇合成速率不会随循环甾醇水平的改变而变化。由于皮肤甾醇可能对通透屏障功能很重要,我们研究了实验性改变的屏障功能对皮肤表皮和真皮层从头甾醇生成的影响。表皮甾醇生成似乎受皮肤屏障需求的调节,因为局部用去污剂和丙酮处理会刺激表皮而非真皮中非皂化脂质的从头合成。合成活性与屏障功能恢复正常的情况以及先前屏障受损的程度均平行。此外,用保鲜膜封闭经溶剂处理的部位可同时纠正屏障异常并使甾醇合成正常化,进一步将表皮甾醇生成增加与屏障需求联系起来。虽然多种其他局部脂质的局部应用并未下调合成,但经皮应用25-羟基胆固醇似乎会减少合成。这些结果表明,维持屏障功能是表皮从头合成非皂化脂质的一个目的,并且进一步证明,尽管缺乏低密度脂蛋白受体,但表皮可根据某些特定需求调节其脂质合成机制。

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