Bioinformatics and Systems Biology Program, Sanford Burnham Medical Research Institute, La Jolla, CA, United States.
Curr Opin Cell Biol. 2012 Feb;24(1):134-40. doi: 10.1016/j.ceb.2011.12.001. Epub 2011 Dec 22.
Adhesions between the cell and the extracellular matrix (ECM) are mechanosensitive multi-protein assemblies that transmit force across the cell membrane and regulate biochemical signals in response to the chemical and mechanical environment. These combined functions in force transduction, signaling and mechanosensing contribute to cellular phenotypes that span development, homeostasis and disease. These adhesions form, mature and disassemble in response to actin organization and physical forces that originate from endogenous myosin activity or external forces by the extracellular matrix. Despite advances in our understanding of the protein composition, interactions and regulation, our understanding of matrix adhesion structure and organization, how forces affect this organization, and how these changes dictate specific signaling events is limited. Insights across multiple structural levels are acutely needed to elucidate adhesion structure and ultimately the molecular basis of signaling and mechanotransduction. Here we describe the challenges and recent advances and prospects for unraveling the structure of cell-matrix adhesions and their response to force.
细胞与细胞外基质(ECM)之间的黏附是机械敏感的多蛋白组装体,可跨细胞膜传递力,并响应化学和机械环境调节生化信号。这些在力转导、信号传递和机械感知方面的综合功能有助于跨越发育、稳态和疾病的细胞表型。这些黏附在肌动蛋白组织和源自内源性肌球蛋白活性或细胞外基质的外力的影响下形成、成熟和解体。尽管我们在蛋白质组成、相互作用和调控方面有了进展,但我们对基质黏附结构和组织、力如何影响这种组织以及这些变化如何决定特定信号事件的理解仍然有限。需要在多个结构水平上进行深入了解,以阐明黏附结构,并最终阐明信号转导和力转导的分子基础。在这里,我们描述了阐明细胞-基质黏附及其对力的响应的结构所面临的挑战以及最近的进展和前景。