Yu Xue-Zhong, Levin Steven D, Madrenas Joaquin, Anasetti Claudio
Human Immunogenetics Program, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
J Immunol. 2004 Feb 1;172(3):1437-43. doi: 10.4049/jimmunol.172.3.1437.
TCR engagement can induce either T cell proliferation and differentiation or activation-induced T cell death (AICD) through apoptosis. The intracellular signaling pathways that dictate such a disparate fate after TCR engagement have only been partially elucidated. Non-FcR-binding anti-CD3 mAbs induce a partial agonist TCR signaling pattern and cause AICD on Ag-activated, cycling T cells. In this study, we examined TCR signaling during the induction of AICD by anti-CD3 fos, a non-FcR-binding anti-CD3 mAb. This mAb activates Fyn, Lck, and extracellular signal-regulated kinase, and induces phosphorylation of Src-like adapter protein, despite the inability to cause calcium mobilization or TCR polarization. Anti-CD3 fos also fails to effectively activate zeta-associated protein of 70 kDa or NF-kappaB. Using Ag-specific T cells deficient for Fyn or Lck, we provide compelling evidence that activation of Lck is required for the induction of AICD. Our data indicate that a selective and distinct TCR signaling pattern is required for AICD by TCR partial agonist ligands.
TCR信号传导可通过凋亡诱导T细胞增殖和分化,或激活诱导的T细胞死亡(AICD)。TCR信号传导后决定这种不同命运的细胞内信号通路仅得到部分阐明。非FcR结合抗CD3单克隆抗体诱导部分激动剂TCR信号模式,并在抗原激活的循环T细胞上导致AICD。在本研究中,我们检测了非FcR结合抗CD3单克隆抗体抗CD3 fos诱导AICD过程中的TCR信号传导。该单克隆抗体激活Fyn、Lck和细胞外信号调节激酶,并诱导Src样衔接蛋白的磷酸化,尽管它无法引起钙动员或TCR极化。抗CD3 fos也不能有效激活70 kDa的ζ相关蛋白或核因子κB。利用缺乏Fyn或Lck的抗原特异性T细胞,我们提供了令人信服的证据,证明Lck的激活是诱导AICD所必需的。我们的数据表明,TCR部分激动剂配体诱导AICD需要一种选择性和独特的TCR信号模式。