Lin R H, Hwang Y W, Yang B C, Lin C S
Graduate Institute of Immunology, College of Medicine, National Taiwan University, Taipei, Republic of China.
J Immunol. 1997 Jan 15;158(2):598-603.
Stimulation of recently activated T cells results in apoptosis of the responding cells, a process referred to as activation-induced cell death. This process is believed to play an important role in the regulation of immune homeostasis and is suggested to be mediated mainly by interactions between Fas and Fas ligand. Recent evidence indicates that TNF-alpha and TNFR2 interaction plays an important role in down-regulating activated T cells. The role of TNFR2 signaling in activation-induced cell death, however, has not been directly examined. We demonstrate here that 48-h activated T cells are most sensitive to TNFR2-induced apoptosis. Cross-linking of TNFR2 on activated T cells results in down-regulated protein and mRNA expression of Bcl-xL. Furthermore, CD28 costimulation can prevent anti-TNFR2-induced apoptosis and restore Bcl-xL expression. These results have potential implications for understanding the role of TNFR2 signaling in the regulation of T cell responses.
对近期激活的T细胞进行刺激会导致应答细胞发生凋亡,这一过程被称为激活诱导的细胞死亡。据信该过程在免疫稳态的调节中发挥重要作用,并且提示主要由Fas与Fas配体之间的相互作用介导。最近的证据表明,TNF-α与TNFR2的相互作用在下调活化T细胞方面发挥重要作用。然而,TNFR2信号传导在激活诱导的细胞死亡中的作用尚未得到直接研究。我们在此证明,激活48小时的T细胞对TNFR2诱导的凋亡最为敏感。活化T细胞上TNFR2的交联导致Bcl-xL的蛋白质和mRNA表达下调。此外,CD28共刺激可预防抗TNFR2诱导的凋亡并恢复Bcl-xL表达。这些结果对于理解TNFR2信号传导在T细胞应答调节中的作用具有潜在意义。