Werlen Guy, Hausmann Barbara, Naeher Dieter, Palmer Ed
Laboratory of Transplantation Immunology and Nephrology, Department of Research, University Hospital-Basel, CH-4031 Basel, Switzerland.
Science. 2003 Mar 21;299(5614):1859-63. doi: 10.1126/science.1067833.
T lymphocytes are generated in the thymus, where developing thymocytes must accept one of two fates: They either differentiate or they die. These fates are chiefly determined by signals that originate from the T cell receptor (TCR), a single receptor complex with a remarkable capacity to decide between distinct cell fates. This review explores TCR signaling in thymocytes and focuses on the kinetic aspects of ligand binding, coreceptor involvement, protein phosphorylation, and mitogen-activated protein kinase (MAPK) activation. Understanding the logic of TCR signaling may eventually explain how thymocytes and T cells distinguish self from nonself, a phenomenon that has fascinated immunologists for 50 years.
T淋巴细胞在胸腺中产生,发育中的胸腺细胞在胸腺中必须接受两种命运之一:要么分化,要么死亡。这些命运主要由源自T细胞受体(TCR)的信号决定,TCR是一种单一的受体复合物,具有在不同细胞命运之间做出决定的非凡能力。本综述探讨了胸腺细胞中的TCR信号传导,并着重于配体结合、共受体参与、蛋白质磷酸化和丝裂原活化蛋白激酶(MAPK)激活的动力学方面。理解TCR信号传导的逻辑最终可能解释胸腺细胞和T细胞如何区分自我与非自我,这一现象已经吸引免疫学家长达50年之久。