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Asymmetric focal adhesion disassembly in motile cells.

机译:运动细胞中不对称粘着斑的拆卸。

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Cell migration requires the integration and coordination of specific focal adhesion dynamics at the cell front, center and rear. In this review, we will present our understanding of the regulation of adhesion turnover and disassembly in various regions of the cell. Adhesion turnover involves a number of tyrosine kinases and phosphatases, most of which are engaged in FAK signaling pathways. Additionally, adhesions are regulated by tensile forces that depend on dynamic coupling with the actin cytoskeleton. The distribution of adhesion disassembly throughout a motile cell is likely coordinated by the asymmetry of the microtubule network. We present a model that suggests two stages of microtubule-driven adhesion disassembly: destabilization and detachment.
机译:细胞迁移需要在细胞的前部,中央和后部整合和协调特定的粘着动力学。在这篇综述中,我们将介绍我们对细胞各个区域的粘附转换和拆卸调控的理解。粘附转换涉及许多酪氨酸激酶和磷酸酶,其中大多数参与FAK信号通路。另外,通过与肌动蛋白细胞骨架动态偶联的张力调节粘附力。粘附拆卸在整个运动细胞中的分布可能通过微管网络的不对称来协调。我们提出了一个模型,该模型建议了微管驱动的粘连拆卸的两个阶段:不稳定和分离。

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