首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Antigen-Dependent Release of IFN-#gamma# by Cytotoxic T Cells Up-Regulates Fas on Target Cells and Facilitates Exocytosis-Independent Specific Target Cell Lysis
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Antigen-Dependent Release of IFN-#gamma# by Cytotoxic T Cells Up-Regulates Fas on Target Cells and Facilitates Exocytosis-Independent Specific Target Cell Lysis

机译:细胞毒性T细胞的抗原依赖性释放IFN-#γ可上调靶细胞上的Fas,并促进不依赖胞吐作用的特异性靶细胞裂解

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摘要

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. Tec 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.
机译:缺乏胞吐作用介导的靶细胞裂解途径的效应细胞溶解性T(Tc)淋巴细胞在靶细胞上诱导Fas,进而通过Fas配体-Fas相互作用延迟细胞死亡和凋亡。 Fas的诱导可以被抗IFN-γγAbs阻断。最初Fas阴性靶细胞的这种Fas上调不是由TCR-MHC /肽信号传导本身介导的,而是由Ag结合后Tc细胞分泌的IFN-γ介导的。 Tc细胞的Fas上调可以通过用rIFN-γγ处理靶细胞来模拟。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。 Tec细胞介导的Fas在第三方,​​旁观者,靶细胞上的表达不会增强其对这些标称效应细胞裂解的敏感性。讨论了该结果与Tc细胞对病毒感染的反应效率和调节的可能相关性。

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