Müllbacher Arno, Lobigs Mario, Hla Ron Tha, Tran Thao, Stehle Thomas, Simon Markus M
Division of Immunology and Cell Biology, John Curtin School of Medical Research, Australian National University, Canberra, Australia.
J Immunol. 2002 Jul 1;169(1):145-50. doi: 10.4049/jimmunol.169.1.145.
Effector cytolytic T (Tc) lymphocytes, deficient in the exocytosis-mediated pathway of target cell lysis, induce Fas on target cells and, in turn, delayed cell death and apoptosis via the Fas ligand-Fas interaction. The induction of Fas can be blocked by anti- IFN-gamma Abs. This Fas up-regulation on initially Fas-negative target cells is not mediated by TCR-MHC/peptide signaling per se, but by secreted IFN-gamma from Tc cells after Ag engagement. The Fas up-regulation by Tc cells can be mimicked by treatment of target cells with rIFN-gamma. Tc cells from IFN-gamma knockout mice do not induce Fas expression on target cells. Tc cell-mediated Fas expression on third party, bystander, target cells does not enhance their susceptibility to lysis by these nominal effector cells. The results are discussed as to the possible relevance of the phenomenon in efficiency and regulation of the Tc cell response to infections by viruses.
效应性细胞毒性T(Tc)淋巴细胞缺乏通过胞吐作用介导的靶细胞裂解途径,它们在靶细胞上诱导Fas表达,进而通过Fas配体与Fas的相互作用导致延迟性细胞死亡和凋亡。Fas的诱导可被抗IFN-γ抗体阻断。最初Fas阴性的靶细胞上Fas的上调并非由TCR-MHC/肽信号本身介导,而是由抗原激活后Tc细胞分泌的IFN-γ介导。用重组IFN-γ处理靶细胞可模拟Tc细胞引起的Fas上调。来自IFN-γ基因敲除小鼠的Tc细胞不会在靶细胞上诱导Fas表达。Tc细胞介导的第三方旁观者靶细胞上的Fas表达不会增强这些名义上的效应细胞对其裂解的敏感性。讨论了该现象与Tc细胞对病毒感染反应的效率和调节的可能相关性。