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白细胞介素-2调节Fas介导的T细胞凋亡的生化机制。

Biochemical mechanisms of IL-2-regulated Fas-mediated T cell apoptosis.

作者信息

Refaeli Y, Van Parijs L, London C A, Tschopp J, Abbas A K

机构信息

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Immunity. 1998 May;8(5):615-23. doi: 10.1016/s1074-7613(00)80566-x.

Abstract

Activation-induced cell death (AICD) of lymphocytes is an important mechanism of self-tolerance. In CD4+ T cells, AICD is mediated by the Fas pathway and is enhanced by IL-2. To define the mechanisms of this pro-apoptotic action of IL-2, we analyzed CD4+ T cells from wild-type and IL-2-/- mice expressing a transgenic T cell receptor. T cells become sensitive to AICD after activation by antigen and IL-2. IL-2 increases transcription and surface expression of Fas ligand (FasL) and suppresses transcription and expression of FLIP, the inhibitor of apoptosis. The ability of IL-2 to enhance expression of a pro-apoptotic molecule, FasL, and to suppress an inhibitor of Fas signaling, FLIP, likely accounts for the role of this cytokine in potentiating T cell apoptosis.

摘要

淋巴细胞的活化诱导细胞死亡(AICD)是自身耐受的重要机制。在CD4+ T细胞中,AICD由Fas途径介导,并被白细胞介素-2(IL-2)增强。为了确定IL-2这种促凋亡作用的机制,我们分析了表达转基因T细胞受体的野生型和IL-2基因敲除小鼠的CD4+ T细胞。T细胞在被抗原和IL-2激活后对AICD变得敏感。IL-2增加Fas配体(FasL)的转录和表面表达,并抑制凋亡抑制剂FLIP的转录和表达。IL-2增强促凋亡分子FasL的表达并抑制Fas信号抑制剂FLIP的能力,可能解释了这种细胞因子在增强T细胞凋亡中的作用。

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