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凌乱蛋白调控纤毛上皮细胞中基体的顶端对接和平面极化。

Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells.

作者信息

Park Tae Joo, Mitchell Brian J, Abitua Philip B, Kintner Chris, Wallingford John B

机构信息

Department of Molecular Cell and Developmental Biology & Institute for Cellular and Molecular Biology, University of Texas, Austin, Texas 78712, USA.

出版信息

Nat Genet. 2008 Jul;40(7):871-9. doi: 10.1038/ng.104. Epub 2008 Jun 15.

Abstract

The planar cell polarity (PCP) signaling system governs many aspects of polarized cell behavior. Here, we use an in vivo model of vertebrate mucociliary epithelial development to show that Dishevelled (Dvl) is essential for the apical positioning of basal bodies. We find that Dvl and Inturned mediate the activation of the Rho GTPase specifically at basal bodies, and that these three proteins together mediate the docking of basal bodies to the apical plasma membrane. Moreover, we find that this docking involves a Dvl-dependent association of basal bodies with membrane-bound vesicles and the vesicle-trafficking protein, Sec8. Once docked, basal bodies again require Dvl and Rho for the planar polarization that underlies directional beating of cilia. These results demonstrate previously undescribed functions for PCP signaling components and suggest that a common signaling apparatus governs both apical docking and planar polarization of basal bodies.

摘要

平面细胞极性(PCP)信号系统控制着极化细胞行为的许多方面。在此,我们利用脊椎动物黏液纤毛上皮发育的体内模型表明,Dishevelled(Dvl)对于基体的顶端定位至关重要。我们发现Dvl和Inturned特异性地在基体处介导Rho GTP酶的激活,并且这三种蛋白质共同介导基体与顶端质膜的对接。此外,我们发现这种对接涉及基体与膜结合囊泡以及囊泡运输蛋白Sec8的Dvl依赖性结合。一旦对接,基体再次需要Dvl和Rho来实现作为纤毛定向摆动基础的平面极化。这些结果证明了PCP信号成分以前未被描述的功能,并表明一种共同的信号装置控制着基体的顶端对接和平面极化。

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