Henning S, Cleverley S
Howard Hughes Medical Institute, Department of Molecular and Cellular Biology, University of California at Berkeley, 94720-3200, USA.
Immunol Res. 1999;20(1):29-42. doi: 10.1007/BF02786505.
Almost a decade ago, the small GTPase Ras was shown to be activated in response to antigen receptor triggering in T cells. Since then, Ras has been further characterized as a central molecule for the regulation of signal transduction pathways in lymphocytes. However, over the last couple of years, its exclusive role in lymphocyte biology has been challenged by the emergence of its relatives of the Rho family. Today it is well established that Rho GTPases act as unique molecular switches at several critical checkpoints in lymphocyte development and function. Additionally, a new and critical concept in GTPase signaling has taken shape over the last couple of years in that small GTPases are able to regulate quite diverse cellular processes in the immune response by linking to multiple biochemical effector pathways.
大约十年前,小GTP酶Ras被证明在T细胞中对抗抗原受体触发时被激活。从那时起,Ras被进一步表征为淋巴细胞中信号转导通路调节的核心分子。然而,在过去几年中,其在淋巴细胞生物学中的独特作用受到了Rho家族相关分子出现的挑战。如今,Rho GTP酶在淋巴细胞发育和功能的几个关键检查点上作为独特的分子开关发挥作用已得到充分证实。此外,在过去几年中,GTP酶信号传导中一个新的关键概念已经形成,即小GTP酶能够通过与多种生化效应通路相连来调节免疫反应中相当多样的细胞过程。