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RhoE是角质形成细胞分化和分层所必需的。

RhoE Is required for keratinocyte differentiation and stratification.

作者信息

Liebig Timo, Erasmus Jennifer, Kalaji Ruba, Davies Derek, Loirand Gervaise, Ridley Anne, Braga Vania M M

机构信息

Molecular Medicine, National Heart and Lung Institute, Imperial College London., United Kingdom.

出版信息

Mol Biol Cell. 2009 Jan;20(1):452-63. doi: 10.1091/mbc.e07-11-1197. Epub 2008 Oct 15.

Abstract

The molecular mechanism via which keratinocyte differentiation assembles multiple layers of cells (stratification) is poorly understood. We describe here a novel function of the Rho family member RhoE as a regulator of epidermal morphogenesis. RhoE protein levels are specifically and transiently up-regulated upon keratinocyte differentiation. RhoE up-regulation requires the activity of Rho kinase (ROCK) I, suggesting that both RhoE and ROCKI are important during keratinocyte differentiation. RhoE overexpression results in a striking enlargement of cell size and the number of stratified cells. In contrast, RhoE depletion induces hyperproliferation and delays initiation of keratinocyte differentiation. Interestingly, up-regulation of RhoE protein is seen primarily in basal, undifferentiated cells, in which commitment to differentiation and stratification takes place. RhoE activation in basal cells negatively modulates integrin adhesion, thereby facilitating detachment from the substratum and migration to form suprabasal layers. Thus, RhoE integrates two processes essential for keratinocyte differentiation and stratification: regulation of proliferative status and integrin adhesion.

摘要

角质形成细胞分化形成多层细胞(分层)的分子机制仍知之甚少。我们在此描述Rho家族成员RhoE作为表皮形态发生调节因子的新功能。角质形成细胞分化时,RhoE蛋白水平会特异性且短暂地上调。RhoE上调需要Rho激酶(ROCK)I的活性,这表明RhoE和ROCKI在角质形成细胞分化过程中都很重要。RhoE过表达导致细胞大小显著增大和分层细胞数量增加。相反,RhoE缺失会诱导过度增殖并延迟角质形成细胞分化的起始。有趣的是,RhoE蛋白上调主要出现在基底未分化细胞中,而细胞在此处开始分化和分层。基底细胞中的RhoE激活会负向调节整合素黏附,从而促进细胞与基质分离并迁移以形成基底上层。因此,RhoE整合了角质形成细胞分化和分层所必需的两个过程:增殖状态调节和整合素黏附。

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