Humphries M J, Travis M A, Clark K, Mould A P
Wellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, University of Manchester, 2.205 Stopford Building, Oxford Road, Manchester M13 9PT, UK.
Biochem Soc Trans. 2004 Nov;32(Pt 5):822-5. doi: 10.1042/BST0320822.
While it is self-evident that all extracellular molecules are an integral part of a multicellular organism, it is paradoxical that they are often considered to be dissociated from cells. The reality is that a continuum of dynamic, bi-directional interactions links the intracellular environment through cell-surface receptors to multimolecular extracellular assemblies. These interactions not only control the behaviour of individual cells, but also determine tissue architecture. Adhesion receptor function is partly determined by an ability to tether the contractile cytoskeleton to the plasma membrane, but there is also evidence that integrin receptors modulate signalling events that are essential for cellular differentiation. A major challenge is now to integrate work at the atomic, molecular and cellular levels, and obtain holistic insights into the mechanisms controlling cell adhesion. In the present study, we review current knowledge of the molecular mechanisms employed by cells to integrate with the extracellular matrix. Two main topics are covered: the adaptation of integrin structure for bi-directional signalling and the integration of integrin signalling with other receptors.
虽然所有细胞外分子都是多细胞生物不可或缺的一部分,这一点不言而喻,但矛盾的是,它们常常被认为与细胞相分离。实际情况是,一系列动态的双向相互作用通过细胞表面受体将细胞内环境与多分子细胞外聚集体联系起来。这些相互作用不仅控制单个细胞的行为,还决定组织结构。黏附受体的功能部分取决于将收缩性细胞骨架系于质膜的能力,但也有证据表明整合素受体可调节对细胞分化至关重要的信号事件。现在的一个主要挑战是整合原子、分子和细胞水平的研究工作,并全面深入了解控制细胞黏附的机制。在本研究中,我们综述了细胞用于与细胞外基质整合的分子机制的现有知识。涵盖了两个主要主题:整合素结构对双向信号传导的适应性以及整合素信号与其他受体的整合。