Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 7610001, Israel.
Department of Biochemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
Biomolecules. 2023 Feb 4;13(2):294. doi: 10.3390/biom13020294.
The interface between the cellular actin network and diverse forms of integrin-mediated cell adhesions displays a unique capacity to serve as accurate chemical and mechanical sensors of the cell's microenvironment. Focal adhesion-like structures of diverse cell types, podosomes in osteoclasts, and invadopodia of invading cancer cells display distinct morphologies and apparent functions. Yet, all three share a similar composition and mode of coupling between a protrusive structure (the lamellipodium, the core actin bundle of the podosome, and the invadopodia protrusion, respectively), and a nearby adhesion site. Cytoskeletal or external forces, applied to the adhesion sites, trigger a cascade of unfolding and activation of key adhesome components (e.g., talin, vinculin, integrin), which in turn, trigger the assembly of adhesion sites and generation of adhesion-mediated signals that affect cell behavior and fate. The structural and molecular mechanisms underlying the dynamic crosstalk between the actin cytoskeleton and the adhesome network are discussed.
细胞肌动蛋白网络与多种形式的整合素介导的细胞黏附之间的界面,具有作为细胞微环境的准确化学和机械传感器的独特能力。不同类型细胞的黏着斑样结构、破骨细胞中的皱襞足和侵袭性癌细胞的侵袭伪足,具有不同的形态和明显的功能。然而,这三者都具有相似的组成和连接方式,即一个突起结构(片状伪足、皱襞足的核心肌动蛋白束和侵袭伪足的突起)和附近的黏附位点之间的连接。施加在黏附位点的细胞骨架或外部力,触发关键黏着斑组件(例如,塔林、纽蛋白、整合素)的级联展开和激活,这反过来又触发黏附位点的组装和黏附介导信号的产生,从而影响细胞行为和命运。本文讨论了肌动蛋白细胞骨架和黏着斑网络之间动态串扰的结构和分子机制。