Lagarrigue Frederic, Kim Chungho, Ginsberg Mark H
Department of Medicine, University of California at San Diego, La Jolla, CA; and.
Department of Life Sciences, Korea University, Seoul, South Korea.
Blood. 2016 Jul 28;128(4):479-87. doi: 10.1182/blood-2015-12-638700. Epub 2016 May 20.
Integrin adhesion receptors mediate the adhesion of blood cells, such as leukocytes, to other cells, such as endothelial cells. Integrins also are critical for anchorage of hematopoietic precursors to the extracellular matrix. Blood cells can dynamically regulate the affinities of integrins for their ligands ("activation"), an event central to their functions. Here we review recent progress in understanding the mechanisms of integrin activation with a focus on the functions of blood cells. We discuss how talin binding to the integrin β cytoplasmic domain, in conjunction with the plasma membrane, induces long-range allosteric rearrangements that lead to integrin activation. Second, we review our understanding of how signaling events, particularly those involving Rap1 small guanosine triphosphate (GTP)hydrolases, can regulate the talin-integrin interaction and resulting activation. Third, we review recent findings that highlight the role of the Rap1-GTP-interacting adapter molecule (RIAM), encoded by the APBB1IP gene, in leukocyte integrin activation and consequently in leukocyte trafficking.
整合素黏附受体介导血细胞(如白细胞)与其他细胞(如内皮细胞)的黏附。整合素对于造血前体细胞锚定到细胞外基质也至关重要。血细胞可以动态调节整合素对其配体的亲和力(“激活”),这是其功能的核心事件。在此,我们综述了在理解整合素激活机制方面的最新进展,重点关注血细胞的功能。我们讨论了踝蛋白与整合素β胞质结构域结合,连同质膜,如何诱导导致整合素激活的远程变构重排。其次,我们综述了我们对信号事件,特别是那些涉及Rap1小GTP酶的信号事件如何调节踝蛋白 - 整合素相互作用及由此产生的激活的理解。第三,我们综述了最近的研究发现,这些发现突出了由APBB1IP基因编码的Rap1 - GTP相互作用衔接分子(RIAM)在白细胞整合素激活以及因此在白细胞迁移中的作用。