The Journal of Experimental Medicine · 1997 · 470 citations · 33 references
Life SciencesCell BiologyImmunologyApoptosisCell SignalingSignal TransductionApoptosis In Immune CellsApoptosis RegulationApoptotic SignalingCell DeathDeath ReceptorsIntrinsic Apoptotic PathwayActivation-induced Cell DeathApoptotic Signaling PathwaysCell ActivationFas LigandFas Ligand-mediated ApoptosisFas Receptor SignalingLag PhaseProgrammed Cell Death Regulation
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.
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bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death
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