Kinashi Tatsuo
Department of Molecular Genetics, Graduate School of Medicine, Institute of Liver Research, Kansai Medical School, 10-15 Fumizono-cho, Moriguchi, Osaka 570-8506, Japan.
Nat Rev Immunol. 2005 Jul;5(7):546-59. doi: 10.1038/nri1646.
Since the discovery that integrins at the surface of lymphocytes undergo dynamic changes in their adhesive activity after stimulation through the T-cell receptor or stimulation with chemokines, intensive research has been carried out in an attempt to clarify the signalling events that lead to the activation of integrins. Whereas structural studies have provided us with a vivid picture of the conformational flexibility of integrins, the signalling pathways that regulate these conformational changes (known as inside-out signalling) have been elusive. However, as I discuss here, recent studies have provided new insight into the pathways that control the regulation of integrin activity and the coordination of complex cellular functions, such as the homing of lymphocytes and the formation of an immunological synapse.
自从发现淋巴细胞表面的整合素在通过T细胞受体刺激或趋化因子刺激后其黏附活性会发生动态变化以来,人们进行了深入研究,试图阐明导致整合素激活的信号传导事件。虽然结构研究为我们提供了整合素构象灵活性的生动图景,但调节这些构象变化的信号通路(称为外向内信号传导)却一直难以捉摸。然而,正如我在此所讨论的,最近的研究为控制整合素活性调节和复杂细胞功能协调(如淋巴细胞归巢和免疫突触形成)的信号通路提供了新的见解。