Mustelin Tomas, Alonso Andres, Bottini Nunzio, Huynh Huong, Rahmouni Souad, Nika Konstantina, Louis-dit-Sully Christine, Tautz Lutz, Togo Summanuna H, Bruckner Shane, Mena-Duran Armando V, al-Khouri Anna Maria
Program of Signal Transduction, Cancer Research Center, The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Mol Immunol. 2004 Jul;41(6-7):687-700. doi: 10.1016/j.molimm.2004.04.015.
The molecular mechanisms of signal transduction have been the focus of intense research during the last decade. In T cells, much of the work has centered on protein tyrosine kinase-mediated signaling from the TCR and cytokine receptors, while the study of protein tyrosine phosphatases has lagged behind. Nevertheless, it has now become clear that many protein tyrosine phosphatases play equally important roles in T cell physiology and that no kinase-regulated system would work without the counterbalancing participation of phosphatases. In fact, we have learned that many processes are regulated primarily on the phosphatase side. This minireview summarizes the current state-of-the art in our understanding of the regulation and biology of protein tyrosine phosphatases in T lymphocyte physiology.
在过去十年中,信号转导的分子机制一直是深入研究的焦点。在T细胞中,许多工作集中于蛋白酪氨酸激酶介导的来自TCR和细胞因子受体的信号传导,而对蛋白酪氨酸磷酸酶的研究则滞后了。然而,现在已经清楚的是,许多蛋白酪氨酸磷酸酶在T细胞生理学中发挥着同样重要的作用,而且没有磷酸酶的平衡参与,激酶调节系统就无法运作。事实上,我们已经了解到许多过程主要是在磷酸酶方面受到调节。这篇微型综述总结了我们目前对T淋巴细胞生理学中蛋白酪氨酸磷酸酶的调节和生物学的理解的最新进展。