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整合素介导的Cdc42激活通过蛋白激酶Cζ调控迁移星形胶质细胞的细胞极性。

Integrin-mediated activation of Cdc42 controls cell polarity in migrating astrocytes through PKCzeta.

作者信息

Etienne-Manneville S, Hall A

机构信息

MRC Laboratory for Molecular Cell Biology, University College London, Gower Street, WC1E 6BT, London, United Kingdom.

出版信息

Cell. 2001 Aug 24;106(4):489-98. doi: 10.1016/s0092-8674(01)00471-8.


DOI:10.1016/s0092-8674(01)00471-8
PMID:11525734
Abstract

We describe here a signal transduction pathway controlling the establishment of mammalian cell polarity. Scratching a confluent monolayer of primary rat astrocytes leads to polarization of cells at the leading edge. The microtubule organizing center, the microtubule cytoskeleton, and the Golgi reorganize to face the new free space, and directed cell protrusion and migration specifically occur perpendicularly to the scratch. We show here that the interaction of integrins with extracellular matrix at the newly formed cell front leads to the activation and polarized recruitment of Cdc42, which in turn recruits and activates a cytoplasmic mPar6/PKCzeta complex. Localized PKCzeta activity, acting through the microtubule motor protein dynein, is required for all aspects of induced polarity in these cells.

摘要

我们在此描述一种控制哺乳动物细胞极性建立的信号转导途径。刮擦原代大鼠星形胶质细胞的汇合单层会导致前沿细胞极化。微管组织中心、微管细胞骨架和高尔基体重新组织以面对新的自由空间,并且定向的细胞突起和迁移特别垂直于刮痕发生。我们在此表明,整合素与新形成的细胞前沿的细胞外基质的相互作用导致Cdc42的激活和极化募集,这反过来又募集并激活细胞质mPar6/PKCzeta复合物。这些细胞中诱导极性的所有方面都需要通过微管运动蛋白动力蛋白起作用的局部PKCzeta活性。

相似文献

[1]
Integrin-mediated activation of Cdc42 controls cell polarity in migrating astrocytes through PKCzeta.

Cell. 2001-8-24

[2]
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[10]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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