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过氧化物酶体增殖物激活受体 δ 的激活促进了妊娠晚期角质层形成和表皮渗透性屏障的发育。

PPARδ activation promotes stratum corneum formation and epidermal permeability barrier development during late gestation.

机构信息

Department of Veterans Affairs Medical Center, Metabolism Section, Veterans Affairs Medical Center, San Francisco, California 94121, USA.

出版信息

J Invest Dermatol. 2010 Feb;130(2):511-9. doi: 10.1038/jid.2009.245. Epub 2009 Aug 13.

DOI:10.1038/jid.2009.245
PMID:19675577
Abstract

The goal of epidermal ontogenesis is to form a stratum corneum (SC), which is required for post-natal permeability barrier function. The regulation of epidermal ontogenesis is poorly understood, but nuclear hormone receptors have been shown to have an important function. As peroxisome proliferator-activated receptor-delta (PPARdelta) is very abundant in fetal epidermis and PPARdelta activation stimulates differentiation and permeability barrier formation in adults, we hypothesized that PPARdelta might regulate epidermal ontogenesis. Treatment of fetal rat explants with the PPARdelta ligand, GW 610742X, accelerates permeability barrier development, evidenced by a decrease in transepidermal water loss and an enhanced outside-in barrier function, attributable to the presence of more mature lamellar membranes in the SC and enhanced expression of loricrin and involucrin. Similarly, the intra-amniotic administration of GW 610742X also accelerates the formation of the SC and permeability barrier development. Finally, in PPARdelta-deficient mice the formation of the SC and the expression of differentiation-related proteins were delayed on days 16.5 and 17.5 of gestation. However, at later stages (day 18.5 and after birth), there were no differences between wild-type- and PPARdelta-deficient mice, indicating only a transient delay in epidermal ontogenesis. These studies show that PPARdelta has a role in SC formation and permeability barrier development.

摘要

表皮发生的目的是形成角质层(SC),这是产后渗透屏障功能所必需的。表皮发生的调节机制尚不清楚,但核激素受体已被证明具有重要功能。由于过氧化物酶体增殖物激活受体-δ(PPARδ)在胎儿表皮中非常丰富,并且 PPARδ 的激活可刺激成人的分化和渗透屏障形成,因此我们假设 PPARδ 可能调节表皮发生。用 PPARδ 配体 GW 610742X 处理胎鼠外植体可加速渗透屏障的发展,这表现在经表皮水分流失减少和外向屏障功能增强,这归因于 SC 中更成熟的板层膜的存在和丝聚蛋白和兜甲蛋白表达增强。同样,GW 610742X 的羊膜内给药也可加速 SC 的形成和渗透屏障的发展。最后,在 PPARδ 缺陷型小鼠中,SC 的形成和分化相关蛋白的表达在妊娠第 16.5 天和第 17.5 天延迟。然而,在后期(第 18.5 天和出生后),野生型和 PPARδ 缺陷型小鼠之间没有差异,这表明表皮发生仅存在短暂的延迟。这些研究表明,PPARδ 在 SC 形成和渗透屏障发展中起作用。

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