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基于显微镜的细胞-基质黏附研究前沿。

Frontiers of microscopy-based research into cell-matrix adhesions.

机构信息

Department of Life Sciences and the National Institute for Biotechnology in the Negev, Ben Gurion University of the Negev, Beer-Sheva 84120, Israel.

出版信息

Curr Opin Cell Biol. 2010 Oct;22(5):659-68. doi: 10.1016/j.ceb.2010.08.006. Epub 2010 Sep 6.

Abstract

Focal adhesions (FAs) are highly dynamic multi-protein complexes, through which cells interact with the extracellular matrix (ECM) via integrin receptors. These large assemblies, which typically measure several micrometers in diameter, mediate interactions of cells with external surfaces, and are linked at their cytoplasmic faces with F-actin bundles. Over the last four decades, the molecular diversity of these adhesions and their roles in cell migration and matrix sensing have been extensively studied. Microscopy-based research is considered critical for characterizing and understanding the nature of these assemblies. Here, we review the contributions of, advanced microscopy to the characterization of the functional architecture of integrin-mediated, cell-matrix adhesions.

摘要

黏着斑是高度动态的多蛋白复合物,通过整合素受体,细胞与细胞外基质(ECM)相互作用。这些大的组装体通常直径测量为几个微米,介导细胞与外部表面的相互作用,并在其细胞质面上与 F-肌动蛋白束相连。在过去的四十年中,这些黏着斑的分子多样性及其在细胞迁移和基质感应中的作用得到了广泛的研究。基于显微镜的研究被认为是对这些组装体的特征和理解其性质的关键。在这里,我们回顾了先进显微镜在整合素介导的细胞-基质黏着功能结构特征中的作用。

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