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黏着斑力学反应中分子变化的多样性模式。

Diverse patterns of molecular changes in the mechano-responsiveness of focal adhesions.

机构信息

Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.

European Bioinformatics Institute, European Molecular Biology Laboratory, Hinxton, Cambridge, UK.

出版信息

Sci Rep. 2018 Feb 1;8(1):2187. doi: 10.1038/s41598-018-20252-0.

Abstract

Focal adhesions anchor contractile actin fibers with the extracellular matrix, sense the generated tension and respond to it by changing their morphology and composition. Here we ask how this mechanosensing is enabled at the protein-network level, given the modular assembly and multitasking of focal adhesions. To address this, we applied a sensitive 4-color live cell imaging approach, enabling monitoring patterns of molecular changes in single focal adhesions. Co-imaging zyxin, FAK, vinculin and paxillin revealed heterogeneities in their responses to Rho-associated kinase (ROCK)-mediated perturbations of actomyosin contractility. These responses were rather weakly correlated between the proteins, reflecting diverse compositional changes in different focal adhesions. This diversity is partially attributable to the location of focal adhesions, their area, molecular content and previous contractility perturbations, suggesting that integration of multiple local cues shapes differentially focal adhesion mechano-responsiveness. Importantly, the compositional changes upon ROCK perturbations exhibited distinct paths in different focal adhesions. Moreover, the protein exhibiting the strongest response to ROCK perturbations varied among different focal adhesions. The diversity in response patterns is plausibly enabled by the modular mode of focal adhesions assembly and can provide them the needed flexibility to perform multiple tasks by combining optimally a common set of multifunctional components.

摘要

黏着斑通过肌动球蛋白纤维与细胞外基质锚定,感知产生的张力,并通过改变其形态和组成来响应张力。在这里,我们想知道,鉴于黏着斑的模块化组装和多功能性,这种机械感应是如何在蛋白质网络层面上实现的。为了解决这个问题,我们应用了一种敏感的四色活细胞成像方法,能够监测单个黏着斑中分子变化的模式。共成像黏着斑蛋白、FAK、 vinculin 和 paxillin,揭示了它们对 Rho 相关激酶 (ROCK) 介导的肌动球蛋白收缩性扰动的反应存在异质性。这些反应在蛋白质之间的相关性较弱,反映了不同黏着斑中不同的组成变化。这种多样性部分归因于黏着斑的位置、面积、分子含量和先前的收缩性扰动,表明多个局部线索的整合会以不同的方式塑造黏着斑的机械响应性。重要的是,ROCK 扰动引起的组成变化在不同的黏着斑中表现出不同的路径。此外,对 ROCK 扰动反应最强的蛋白质在不同的黏着斑中也不同。不同黏着斑的响应模式的多样性可能是由黏着斑组装的模块化模式所允许的,并且可以通过最佳地组合一组通用的多功能组件,为其提供执行多个任务所需的灵活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/5795008/4a7bf5ad8675/41598_2018_20252_Fig1_HTML.jpg

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