Gourley T S, Chang C H
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
J Immunol. 2001 Mar 1;166(5):2917-21. doi: 10.4049/jimmunol.166.5.2917.
The Fas:Fas ligand pathway is critical in regulating immune homeostasis by eliminating activated T cells that proliferated in response to an infection. Here, we show that the MHC class II transactivator (CIITA) can suppress this pathway by inhibiting transcription of the Fas ligand gene. CIITA can effectively repress transcription from the Fas ligand promoter in both T cell lines as well as primary cells. The repression appears to be at least partly due to interference of NFAT-mediated induction of Fas ligand gene transcription. T cells that express CIITA constitutively do not up-regulate Fas ligand on the cell surface after activation via the TCR. Consequently, these cells lack the ability to undergo activation-induced cell death, and to kill Fas-bearing target cells.
Fas:Fas配体途径在通过清除因感染而增殖的活化T细胞来调节免疫稳态方面至关重要。在此,我们表明MHC II类反式激活因子(CIITA)可通过抑制Fas配体基因的转录来抑制该途径。CIITA可有效抑制T细胞系和原代细胞中Fas配体启动子的转录。这种抑制似乎至少部分是由于NFAT介导的Fas配体基因转录诱导受到干扰。组成性表达CIITA的T细胞在通过TCR激活后,细胞表面的Fas配体不会上调。因此,这些细胞缺乏经历激活诱导的细胞死亡以及杀伤携带Fas的靶细胞的能力。