免疫學研究所CHIA, HUANG SHIHHUANG SHIHCHIATSAI, HWEI-FANGHWEI-FANGTSAITZENG, HORNG-TAYHORNG-TAYTZENGLIAO, HSIU-JUNGHSIU-JUNGLIAOHSU, PING-NINGPING-NINGHSU2012-07-092018-07-092012-07-092018-07-092011http://ntur.lib.ntu.edu.tw//handle/246246/240945The TNF-related apoptosis-inducing ligand was shown to provide a costimulatory signal that cooperates with the TCR/ CD3 complex to induce T cell proliferation and cytokine production. Although a number of signaling pathways were linked to the TCR/CD3 complex, it is not known how these two receptors cooperate to induce T cell activation. In this study, we show that TRAIL-induced costimulation of T cells depends on activation of the NF- B pathway. TRAIL induced the NF- B pathway by phosphorylation of inhibitor of B factor kinase and protein kinase C in conjunction with anti-CD3. Furthermore, we demonstrated that TRAIL costimulation induced phosphorylation of the upstream TCR- proximal tyrosine kinases, Lck and ZAP70. Ligation of the TRAIL by its soluble receptor, DR4-Fc, alone was able to induce the phosphorylation of Lck and ZAP70 and to activate the NF- B pathway; however, it was insufficient to fully activate T cells to support T cell proliferation. In contrast, TRAIL engagement in conjunction with anti-CD3, but not TRAIL ligation alone, induced lipid raft assembly and recruitment of Lck and PKC . These results demonstrate that TRAIL costimulation mediates NF- B activation and T cell proliferation by lipid raft assembly and recruitment of Lck. Our results suggest that in TRAIL costimulation, lipid raft recruitment of Lck integrates mitogenic NF- B–dependent signals from the TCR and TRAIL in T lymphocytes.en-US