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Microtubules meet substrate adhesions to arrange cell polarity.

机译:微管与底物粘附,以排列细胞极性。

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Cell movement is driven by the regulated and polarised turnover of the actin cytoskeleton and of the adhesion complexes that link it to the extracellular matrix. For most cells, polarisation requires the engagement of microtubules, which exert their effect by mediating changes in the activity of the Rho GTPases. Evidence suggests that these changes are effected in a very localised fashion at sites of substrate adhesion, via specific microtubule-targeting interactions. Targeting serves to bring molecular complexes bound at the tips and along microtubules in close proximity with adhesion complexes, to promote adhesion disassembly and remodelling of the actin cytoskeleton.
机译:肌动蛋白细胞骨架以及将其连接至细胞外基质的粘附复合物的调节和极化转换驱动细胞运动。对于大多数细胞,极化需要微管的参与,微管通过介导Rho GTPases活性的变化发挥作用。有证据表明,这些变化是通过特定的微管靶向相互作用以非常局部的方式在底物粘附位点实现的。靶向作用是使结合在尖端和沿着微管的分子复合物与粘附复合物紧密接近,以促进肌动蛋白细胞骨架的粘附分解和重塑。

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