Department of Chemistry, Stanford University, Stanford, CA, USA.
Wu-Tsai Neuroscience Institute and ChEM-H institute, Stanford University, Stanford, CA, USA.
Nat Cell Biol. 2023 Oct;25(10):1453-1464. doi: 10.1038/s41556-023-01238-1. Epub 2023 Sep 28.
Integrin-mediated focal adhesions are the primary architectures that transmit forces between the extracellular matrix (ECM) and the actin cytoskeleton. Although focal adhesions are abundant on rigid and flat substrates that support high mechanical tensions, they are sparse in soft three-dimensional (3D) environments. Here we report curvature-dependent integrin-mediated adhesions called curved adhesions. Their formation is regulated by the membrane curvatures imposed by the topography of ECM protein fibres. Curved adhesions are mediated by integrin ɑvβ5 and are molecularly distinct from focal adhesions and clathrin lattices. The molecular mechanism involves a previously unknown interaction between integrin β5 and a curvature-sensing protein, FCHo2. We find that curved adhesions are prevalent in physiological conditions, and disruption of curved adhesions inhibits the migration of some cancer cell lines in 3D fibre matrices. These findings provide a mechanism for cell anchorage to natural protein fibres and suggest that curved adhesions may serve as a potential therapeutic target.
整联蛋白介导的黏附斑是细胞外基质(ECM)和肌动蛋白细胞骨架之间传递力的主要结构。尽管黏附斑在刚性和平坦的基底上很丰富,这些基底能够支持较高的机械张力,但在柔软的三维(3D)环境中却很稀少。在这里,我们报告了一种称为弯曲黏附的曲率依赖性整联蛋白介导的黏附。它们的形成受到 ECM 蛋白纤维拓扑结构产生的膜曲率的调节。弯曲黏附由整合素 ɑvβ5 介导,在分子水平上与黏附斑和笼蛋白晶格不同。分子机制涉及整合素β5 与一种未知的曲率感应蛋白 FCHo2 之间的先前未知的相互作用。我们发现弯曲黏附在生理条件下很普遍,并且破坏弯曲黏附会抑制一些癌细胞系在 3D 纤维基质中的迁移。这些发现为细胞附着到天然蛋白纤维提供了一种机制,并表明弯曲黏附可能成为一个潜在的治疗靶点。