首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Cutting edge:cellular fas-associated death domain-like IL-1-converting enzyme-inhibitory protein protects germinal center B cells from apoptosis during germinal center reactions
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Cutting edge:cellular fas-associated death domain-like IL-1-converting enzyme-inhibitory protein protects germinal center B cells from apoptosis during germinal center reactions

机译:前沿:细胞Fas相关死亡域样IL-1转化酶抑制蛋白可保护生发中心B细胞在生发中心反应过程中免于凋亡

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摘要

During germinal center (GC) reactions, follicular dendritic cells are believed to select memory B lymphocytes by switching off apoptosis in the successfully binding B cells. The cellular signals involved in this process are largely unknown. Here, we show that GC B lymphocytes have a long isoform of the cel-lular homologue of the viral Fas-associated death domain-like Lb-i-converting enzyme-like inhibitory protein (cFLIPL), which is capable of inhibiting death receptor-induced caspase activation. In isolated GC B cells, cFLIPL decays rapidly even without Fas ligation, and this results in activation of caspase activity and apoptosis. Contact with follicular dendritic cells prevents cFLIPL degradation and blocks all signs of apoptosis, even in the presence of anti-Fas Abs. cFLIPL expression is sustained by CD4O ligation as well, suggesting that at least at some stage of the GC reaction activated T cells may help se-lected B cells to leave the follicular dendritic cell network with-out becoming apoptotic.
机译:在生发中心(GC)反应期间,滤泡树突状细胞被认为可以通过关闭成功结合的B细胞的凋亡来选择记忆B淋巴细胞。在此过程中涉及的细胞信号很大程度上未知。在这里,我们显示GC B淋巴细胞具有病毒Fas相关死亡域样Lb-i转换酶样抑制蛋白(cFLIPL)的细胞同源物的长同工型,它能够抑制死亡受体-诱导胱天蛋白酶激活。在分离的GC B细胞中,即使没有Fas连接,cFLIPL也会迅速衰减,这导致caspase活性激活和凋亡。与滤泡树突状细胞的接触可防止cFLIPL降解并阻止所有凋亡迹象,即使存在抗Fas抗体也是如此。 cFLIPL表达也可通过CD4O连接来维持,这表明至少在GC反应的某个阶段,活化的T细胞可能有助于选择的B细胞离开滤泡树突状细胞网络而不会凋亡。

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