首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Unequal Death in T Helper Cell (Th)1 and Th2 Effectors: Th1 but not Th2 Effectors Undergo Rapid Fas/FasL-mediated Apoptosis
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Unequal Death in T Helper Cell (Th)1 and Th2 Effectors: Th1 but not Th2 Effectors Undergo Rapid Fas/FasL-mediated Apoptosis

机译:T辅助细胞(Th)1和Th2效应子中的不平等死亡:Th1但非Th2效应子经历Fas / FasL介导的快速凋亡

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摘要

T helper cell (Th) 1, but not Th2, effectors undergo rapid Fas/Fas ligand (FasL)-mediated, activation-induced cell death upon restimulation with antigen. Unequal apoptosis is also observed without restimulation, after a longer lag period. Both effectors undergo delayed apoptosis induced by a non–Fas-mediated pathway. When Th1 and Th2 effectors are co-cultured, Th2 effectors survive preferentially, suggesting the responsible factor(s) is intrinsic to each population. Both Th1 and Th2 effectors express Fas and FasL, but only Th2 effectors express high levels of FAP-1, a Fas-associated phosphatase that may act to inhibit Fas signaling. The rapid death of Th1 effectors leading to selective Th2 survival provides a novel mechanism for differential regulation of the two subsets.
机译:T辅助细胞(Th)1,而不是Th2,效应子在用抗原再刺激后会经历快速的Fas / Fas配体(FasL)介导的激活诱导的细胞死亡。在较长的滞后时间后,在没有重新刺激的情况下也观察到不相等的凋亡。两种效应子均经历由非Fas介导的途径诱导的延迟凋亡。当共同培养Th1和Th2效应子时,Th2效应子优先存活,这表明每个种群固有的责任因子。 Th1和Th2效应子都表达Fas和FasL,但是只有Th2效应子表达高水平的FAP-1,FAP-1是Fas相关的磷酸酶,可抑制Fas信号转导。 Th1效应物的快速死亡导致选择性Th2存活,为差异调节这两个亚群提供了一种新颖的机制。

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