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A Highlights from MBoC Selection: Stretch-induced actin remodeling requires targeting of zyxin to stress fibers and recruitment of actin regulators

机译:MBoC选择的亮点:拉伸诱导的肌动蛋白重塑需要将酶原靶向应力纤维并募集肌动蛋白调节剂

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摘要

Reinforcement of actin stress fibers in response to mechanical stimulation depends on a posttranslational mechanism that requires the LIM protein zyxin. The C-terminal LIM region of zyxin directs the force-sensitive accumulation of zyxin on actin stress fibers. The N-terminal region of zyxin promotes actin reinforcement even when Rho kinase is inhibited. The mechanosensitive integrin effector p130Cas binds zyxin but is not required for mitogen-activated protein kinase–dependent zyxin phosphorylation or stress fiber remodeling in cells exposed to uniaxial cyclic stretch. α-Actinin and Ena/VASP proteins bind to the stress fiber reinforcement domain of zyxin. Mutation of their docking sites reveals that zyxin is required for recruitment of both groups of proteins to regions of stress fiber remodeling. Zyxin-null cells reconstituted with zyxin variants that lack either α-actinin or Ena/VASP-binding capacity display compromised response to mechanical stimulation. Our findings define a bipartite mechanism for stretch-induced actin remodeling that involves mechanosensitive targeting of zyxin to actin stress fibers and localized recruitment of actin regulatory machinery.
机译:响应于机械刺激的肌动蛋白应激纤维的增强取决于需要LIM蛋白酶的翻译后机制。 zyxin的C末端LIM区域指导zyxin在肌动蛋白应激纤维上的力敏感积累。甚至在Rho激酶被抑制时,zyxin的N末端区域也会促进肌动蛋白的增强。机械敏感的整联蛋白效应子p130Cas与zyxin结合,但是在暴露于单轴循环拉伸的细胞中,丝裂素激活的蛋白激酶依赖性酶的磷酸化或应力纤维重塑不是必需的。 α-肌动蛋白和Ena / VASP蛋白与酶的应激纤维增强结构域结合。它们的停靠位点的突变表明,需要酶才能将两组蛋白质募集到应力纤维重塑区域。用缺乏α-肌动蛋白或Ena / VASP结合能力的zyxin变体重组的Zyxin无细胞显示出对机械刺激的反应减弱。我们的研究结果定义了牵拉诱导的肌动蛋白重塑的两方机制,涉及酶对肌动蛋白应力纤维的机械敏感性靶向和肌动蛋白调节机制的局部募集。

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