Arana Eloisa, Harwood Naomi E, Batista Facundo D
Lymphocyte Interaction Laboratory, Cancer Research UK London Research Institute, Lincoln's Inn Fields Laboratories, London WC2A 3PX, UK.
J Cell Sci. 2008 Jul 15;121(Pt 14):2279-86. doi: 10.1242/jcs.017905.
Effective immune surveillance is absolutely dependent on the migration of lymphocytes throughout the body and on their successful recognition of specific antigens. Both of these functions rely on the capacity of integrins that are expressed on the surface of lymphocytes to respond in a highly regulated manner to a variety of chemokines and antigens. This Commentary is primarily concerned with the role of the B-cell integrins LFA-1 and VLA-4 in the antigen-recognition process, and summarises what is currently known about the molecular mechanisms of ;inside-out' integrin activation in response to B-cell-receptor stimulation. Recent investigations have identified Vav, PI3K and small GTPases as crucial regulators of the inside-out activation of B-cell integrins. These observations are of particular interest as they allude to an underlying mechanism by which B-cell-receptor-mediated signalling is linked to cytoskeleton reorganisation and subsequent integrin activation.
有效的免疫监视绝对依赖于淋巴细胞在全身的迁移以及它们对特定抗原的成功识别。这两种功能都依赖于淋巴细胞表面表达的整合素以高度调节的方式对多种趋化因子和抗原作出反应的能力。本述评主要关注B细胞整合素LFA-1和VLA-4在抗原识别过程中的作用,并总结目前已知的B细胞受体刺激后“由内向外”整合素激活的分子机制。最近的研究已确定Vav、PI3K和小GTP酶是B细胞整合素由内向外激活的关键调节因子。这些观察结果特别令人感兴趣,因为它们暗示了一种潜在机制,通过该机制B细胞受体介导的信号传导与细胞骨架重组及随后的整合素激活相联系。