Tai T-S, Fang L-W, Lai M-Z
Graduate Institute of Immunology, National Taiwan University, Taipei, Taiwan, ROC.
Cell Death Differ. 2004 Jan;11(1):69-79. doi: 10.1038/sj.cdd.4401316.
Cellular FLICE-inhibitory protein (c-FLIP) inhibits death receptor-mediated apoptosis by specific interaction with FADD and procaspase-8, and may thus interfere with activation events mediated by FADD and caspase-8. Recent studies, however, suggest that c-FLIP also transmits activation signals. The role of c-FLIP on T-cell activation was examined here using several transgenic mice with variable c-FLIP expression. In all c-FLIP-transgenic mice, Fas-mediated apoptosis and in vitro activation-induced T-cell death were suppressed, and T-cell proliferation and IL-2 production were inhibited. c-FLIP transgene also promoted in vivo thymocyte death. Higher c-FLIP transgene expression was correlated with a more profound suppression of T-cell activation and a prominent disturbance in mature thymocyte development. There was no evidence of increased activation and proliferation in all c-FLIP-transgenic T cells examined. Instead, suppression of T-cell activation in c-FLIP-transgenic T cells could be a combinatory effect of FADD/caspase-8-dependent signals and c-FLIP-specific activities.
细胞型FLICE抑制蛋白(c-FLIP)通过与FADD和procaspase-8特异性相互作用来抑制死亡受体介导的细胞凋亡,因此可能会干扰由FADD和caspase-8介导的激活事件。然而,最近的研究表明,c-FLIP也能传递激活信号。本文利用几只c-FLIP表达量不同的转基因小鼠研究了c-FLIP在T细胞激活中的作用。在所有c-FLIP转基因小鼠中,Fas介导的细胞凋亡以及体外激活诱导的T细胞死亡均受到抑制,T细胞增殖和IL-2产生也受到抑制。c-FLIP转基因还促进了体内胸腺细胞死亡。较高的c-FLIP转基因表达与T细胞激活的更显著抑制以及成熟胸腺细胞发育的明显紊乱相关。在所检测的所有c-FLIP转基因T细胞中,均未发现激活和增殖增加的证据。相反,c-FLIP转基因T细胞中T细胞激活的抑制可能是FADD/caspase-8依赖性信号和c-FLIP特异性活性的联合作用。