Valdembri Donatella, Sandri Chiara, Santambrogio Martina, Serini Guido
Laboratory of Cell Adhesion Dynamics-IRCC, Institute for Cancer Research and Treatment and Department of Oncological Sciences, University of Torino School of Medicine, Strada Provinciale 142, Km 3.95, 10060, Candiolo, Italy.
Mol Biosyst. 2011 Sep;7(9):2539-46. doi: 10.1039/c1mb05066d. Epub 2011 Jul 15.
In multicellular organisms, the execution of complex morphogenetic events, such as gastrulation or vascular morphogenesis, depends on the dynamic modulation of adhesion. Guidance cues, such as chemokines, growth factors, and semaphorins control the attachment of cells to extracellular matrix proteins by regulating the conformational activation of integrin receptors. The endo-exocytic traffic of integrins back and forth from the plasma membrane represents another crucial regulatory aspect in cell adhesion and motility. Recent work added an additional layer of complexity by indicating that distinct molecular machineries are required for trafficking active and inactive integrins.
在多细胞生物中,复杂形态发生事件(如原肠胚形成或血管形态发生)的执行取决于黏附的动态调节。趋化因子、生长因子和信号素等引导信号通过调节整合素受体的构象激活来控制细胞与细胞外基质蛋白的附着。整合素在质膜内外的胞吞胞吐运输是细胞黏附和运动的另一个关键调节方面。最近的研究表明,运输活性和非活性整合素需要不同的分子机制,这增加了一层复杂性。