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The Rac activator Tiam1 is required for polarized protrusional outgrowth of primary astrocytes by affecting the organization of the microtubule network

机译:Rac激活剂Tiam1通过影响微管网络的组织对于原代星形胶质细胞的极化突出生长是必需的

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摘要

Polarized cell migration is a crucial process in the development and repair of tissues, as well as in pathological conditions, including cancer. Recent studies have elucidated important roles for Rho GTPases in the establishment and maintenance of polarity prior to and during cell migration. Here, we show that Tiam1, a specific activator of the small GTPase Rac, is required for the polarized outgrowth of protrusions in primary astrocytes during the initial phase of cell polarization after scratch-wounding monolayers of cells. Tiam1 deficiency delays closure of wounds in confluent monolayers. Lack of Tiam1 impairs adoption of an asymmetrical cell shape as well as microtubule organization within protrusions. Positioning of the centrosome and Golgi apparatus, however, are independent of Tiam1-Rac signaling. We speculate that the function of Tiam1 in polarized outgrowth of astrocyte protrusions involves regulation of microtubule organization, possibly by stabilizing the microtubule cytoskeleton. Our results add Tiam1 as a player to the growing list of proteins involved in polarized outgrowth of protrusions and further elucidate the signaling pathways leading to cell polarization.
机译:极化的细胞迁移是组织发育和修复以及病理状况(包括癌症)中的关键过程。最近的研究阐明了Rho GTPases在细胞迁移之前和期间极性建立和维持中的重要作用。在这里,我们显示Tiam1,一种小GTPase Rac的特定活化剂,对于单层细胞划伤后的细胞极化初始阶段中,原代星形胶质细胞突起的极化增长是必需的。 Tiam1缺乏症会延迟融合单层伤口的闭合。 Tiam1的缺乏会损害不对称细胞形状以及突起内微管组织的采用。然而,中心体和高尔基体的定位与Tiam1-Rac信号传导无关。我们推测,Tiam1在星形胶质细胞突起的极化向外生长中的功能涉及调节微管的组织,可能是通过稳定微管的细胞骨架来实现的。我们的研究结果使Tiam1作为参与突起极化增长的蛋白质列表的参与者,并进一步阐明了导致细胞极化的信号传导途径。

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