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糖皮质激素缺乏会延迟胎鼠角质层的成熟。

Glucocorticoid deficiency delays stratum corneum maturation in the fetal mouse.

作者信息

Hanley K, Feingold K R, Kömüves L G, Elias P M, Muglia L J, Majzoub J A, Williams M L

机构信息

Department of Dermatology, University of California, San Francisco 94143-0316, USA.

出版信息

J Invest Dermatol. 1998 Sep;111(3):440-4. doi: 10.1046/j.1523-1747.1998.00303.x.

DOI:10.1046/j.1523-1747.1998.00303.x
PMID:9740238
Abstract

The stratum corneum (SC) matures during late gestation in man and other mammals. Using the fetal rat as an experimental model, we have previously shown that glucocorticoids given in pharmacologic doses accelerate fetal SC maturation and barrier formation. To determine whether glucocorticoids are required for normal SC maturation, we examined the epidermal morphology of glucocorticoid-deficient (C-) murine pups, derived from matings of mice homozygous for null mutations of the corticotropin-releasing hormone alleles. In control pups on day 17.5 of gestation (term is 19.5 d), a multilayered SC was present and neutral lipid deposition in a membrane pattern was observed using Nile red fluorescence histochemistry. Ultrastructurally, mature lamellar unit structures predominate in the SC intercellular domains. In contrast, in C-pups only a single layer of SC was evident on day 17.5, and secreted lamellar material was not organized into mature lamellar structures. Furthermore, the expression of structural proteins necessary for cornified envelope formation, involucrin, loricrin, and filaggrin, and the activity of the lipid synthetic enzymes beta-glucocerebrosidase and steroid sulfatase, markers of barrier maturation, were reduced in day 17.5 C-pups. C-pups derived from pregnancies supplemented with physiologic amounts of cortisone, however, display normal SC ultrastructure on day 17.5 of gestation. Furthermore, at birth, both control and C-pups exhibit a multilayered SC replete with mature lamellar membrane structures. These data demonstrate that fetal glucocorticoid deficiency delays SC maturation, and suggests that normal levels of glucocorticoids are not absolutely required for SC development.

摘要

在人类和其他哺乳动物中,角质层(SC)在妊娠后期成熟。我们先前以胎鼠作为实验模型,发现给予药理剂量的糖皮质激素可加速胎儿SC成熟和屏障形成。为了确定正常的SC成熟是否需要糖皮质激素,我们检查了促肾上腺皮质激素释放激素等位基因纯合无效突变小鼠交配产生的糖皮质激素缺乏(C-)小鼠幼崽的表皮形态。在妊娠第17.5天(足月为19.5天)的对照幼崽中,存在多层SC,使用尼罗红荧光组织化学观察到中性脂质以膜模式沉积。超微结构上,成熟的板层单位结构在SC细胞间区域占主导。相比之下,在C-幼崽中,在第17.5天仅可见单层SC,并且分泌的板层物质未组织成成熟的板层结构。此外,在第17.5天的C-幼崽中,角质包膜形成所需的结构蛋白、内披蛋白、兜甲蛋白和丝聚合蛋白的表达以及脂质合成酶β-葡萄糖脑苷脂酶和类固醇硫酸酯酶的活性(屏障成熟的标志物)均降低。然而,来自补充生理量可的松的妊娠的C-幼崽在妊娠第17.5天显示正常的SC超微结构。此外,在出生时,对照幼崽和C-幼崽均表现出具有成熟板层膜结构的多层SC。这些数据表明胎儿糖皮质激素缺乏会延迟SC成熟,并表明糖皮质激素的正常水平并非SC发育绝对必需的。

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