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奇美拉蛋白在顶端膜抑制 Rac1 的激活以维持囊泡结构。

Chimaerin suppresses Rac1 activation at the apical membrane to maintain the cyst structure.

机构信息

Laboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University, Yoshida Konoe-cho, Sakyo-ku, Kyoto, Japan.

出版信息

PLoS One. 2012;7(12):e52258. doi: 10.1371/journal.pone.0052258. Epub 2012 Dec 20.

Abstract

Epithelial organs are made of a well-polarized monolayer of epithelial cells, and their morphology is maintained strictly for their proper functions. Previously, we showed that Rac1 activation is suppressed at the apical membrane in the mature organoid, and that such spatially biased Rac1 activity is required for the polarity maintenance. Here we identify Chimaerin, a GTPase activating protein for Rac1, as a suppressor of Rac1 activity at the apical membrane. Depletion of Chimaerin causes over-activation of Rac1 at the apical membrane in the presence of hepatocyte growth factor (HGF), followed by luminal cell accumulation. Importantly, Chimaerin depletion did not inhibit extension formation at the basal membrane. These observations suggest that Chimaerin functions as the apical-specific Rac1 GAP to maintain epithelial morphology.

摘要

上皮组织由具有良好极性的单层上皮细胞组成,其形态严格维持其正常功能。以前,我们发现 Rac1 的激活在成熟类器官的顶膜中受到抑制,而这种空间偏向的 Rac1 活性对于极性的维持是必需的。在这里,我们确定 Chimaerin(Rac1 的 GTP 酶激活蛋白)是顶膜中 Rac1 活性的抑制剂。在存在肝细胞生长因子 (HGF) 的情况下,Chimaerin 的耗竭会导致 Rac1 在顶膜过度激活,随后出现腔细胞积聚。重要的是,Chimaerin 的耗竭并不抑制基底膜的延伸形成。这些观察结果表明,Chimaerin 作为顶膜特异性 Rac1 GAP 发挥作用,以维持上皮形态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c31/3527519/3eecb9e4fe99/pone.0052258.g001.jpg

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