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塔林和伴肌球蛋白协同控制整合素簇的密度。

Talin and kindlin cooperate to control the density of integrin clusters.

机构信息

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France.

Aix Marseille Univ, CNRS, CINAM, Turing Centre for Living Systems, Marseille, France.

出版信息

J Cell Sci. 2023 Apr 15;136(8). doi: 10.1242/jcs.260746. Epub 2023 Apr 21.

Abstract

Focal adhesions are composed of transmembrane integrins, linking the extracellular matrix to the actomyosin cytoskeleton, via cytoplasmic proteins. Adhesion depends on the activation of integrins. Talin and kindlin proteins are intracellular activators of integrins that bind to β-integrin cytoplasmic tails. Integrin activation and clustering through extracellular ligands guide the organization of adhesion complexes. However, the roles of talin and kindlin in this process are poorly understood. To determine the contribution of talin, kindlin, lipids and actomyosin in integrin clustering, we used a biomimetic in vitro system, made of giant unilamellar vesicles, containing transmembrane integrins (herein αIIbβ3), with purified talin (talin-1), kindlin (kindlin-2, also known as FERMT2) and actomyosin. Here, we show that talin and kindlin individually have the ability to cluster integrins. Talin and kindlin synergize to induce the formation of larger integrin clusters containing the three proteins. Comparison of protein density reveals that kindlin increases talin and integrin density, whereas talin does not affect kindlin and integrin density. Finally, kindlin increases integrin-talin-actomyosin coupling. Our study unambiguously demonstrates how kindlin and talin cooperate to induce integrin clustering, which is a major parameter for cell adhesion.

摘要

黏着斑由跨膜整合素组成,通过细胞质蛋白将细胞外基质与肌动球蛋白细胞骨架连接起来。黏附取决于整合素的激活。桩蛋白和伴肌动蛋白是整合素的细胞内激活剂,与β整合素胞质尾部结合。整合素通过细胞外配体的激活和聚集引导黏附复合物的形成。然而,桩蛋白和伴肌动蛋白在这个过程中的作用还知之甚少。为了确定桩蛋白、伴肌动蛋白、脂质和肌动球蛋白在整合素聚集中的作用,我们使用了一种仿生体外系统,由含有跨膜整合素(此处为αIIbβ3)的巨大单层囊泡组成,并用纯化的桩蛋白(桩蛋白-1)、伴肌动蛋白(也称为 FERMT2)和肌动球蛋白处理。在这里,我们表明桩蛋白和伴肌动蛋白各自具有聚集整合素的能力。桩蛋白和伴肌动蛋白协同作用诱导形成包含这三种蛋白的更大的整合素簇。比较蛋白质密度表明,伴肌动蛋白增加了桩蛋白和整合素的密度,而桩蛋白不影响伴肌动蛋白和整合素的密度。最后,伴肌动蛋白增加了整合素-桩蛋白-肌动球蛋白的偶联。我们的研究明确证明了伴肌动蛋白和桩蛋白如何协同诱导整合素聚集,这是细胞黏附的一个主要参数。

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