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新生大鼠角质层中性pH值的功能后果

Functional consequences of a neutral pH in neonatal rat stratum corneum.

作者信息

Fluhr Joachim W, Mao-Qiang Man, Brown Barbara E, Hachem Jean-Pierre, Moskowitz David G, Demerjian Marianne, Haftek Marek, Serre Guy, Crumrine Debra, Mauro Theodora M, Elias Peter M, Feingold Kenneth R

机构信息

Dermatology and Medical Service, Veterans Affairs Medical Center, San Francisco, California 94121, USA.

出版信息

J Invest Dermatol. 2004 Jul;123(1):140-51. doi: 10.1111/j.0022-202X.2004.22726.x.

Abstract

At birth, neonatal stratum corneum (SC) pH is close to neutral but acidifies with maturation, which can be ascribed, in part, to secretory phospholipase A(2) and sodium/hydrogen antiporter 1 (NHE1) activities. Here we assessed the functional consequences of a neutral SC pH in a newborn rat model. While basal transepidermal water loss rates are near normal, barrier recovery (BR) rates after acute barrier disruption were delayed in newborn animals. The abnormality in barrier homeostasis could be improved by topical applications of an acidic buffer, indicating that barrier abnormality is primarily due to high SC pH. The delay in BR correlated with incompletely processed lamellar membranes and decreased activity of beta-glucocerebrosidase. Inhibition of NHE1 delayed BR after acute barrier perturbation. SC integrity was abnormal in newborn animals. Electron microscopy demonstrated decreased corneodesmosomes (CD) in newborn animals with decreased expression of desmoglein 1 and corneodesmosin. Serine protease activation appears to be responsible for CD degradation in newborn animals, because serine protease activity is increased in the SC and it can be reduced by acidification of the SC. The delay in acidification of neonatal SC results in abnormalities in permeability barrier homeostasis and SC integrity and are likely due to pH-induced modulations in enzyme activity.

摘要

出生时,新生儿角质层(SC)的pH值接近中性,但随着成熟而酸化,这部分可归因于分泌型磷脂酶A2和钠/氢反向转运蛋白1(NHE1)的活性。在此,我们在新生大鼠模型中评估了中性SC pH值的功能后果。虽然基础经表皮水分流失率接近正常,但新生动物急性屏障破坏后的屏障恢复(BR)率延迟。屏障稳态异常可通过局部应用酸性缓冲液得到改善,表明屏障异常主要是由于SC pH值高。BR延迟与板层膜加工不完全以及β-葡萄糖脑苷脂酶活性降低有关。NHE1的抑制在急性屏障扰动后延迟了BR。新生动物的SC完整性异常。电子显微镜显示新生动物的角质形成细胞桥粒(CD)减少,桥粒芯糖蛋白1和桥粒芯蛋白的表达降低。丝氨酸蛋白酶激活似乎是新生动物CD降解的原因,因为SC中的丝氨酸蛋白酶活性增加,并且通过SC酸化可以降低其活性。新生儿SC酸化延迟导致通透性屏障稳态和SC完整性异常,这可能是由于pH诱导的酶活性调节所致。

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