| Literature DB >> 11911831 |
Thi Sau Migone1, Jun Zhang, Xia Luo, Li Zhuang, Cecil Chen, Bugen Hu, June S Hong, James W Perry, Su Fang Chen, Joe X H Zhou, Yun Hee Cho, Stephen Ullrich, Palanisamy Kanakaraj, Jeffrey Carrell, Ernest Boyd, Henrik S Olsen, Gang Hu, Laurie Pukac, Ding Liu, Jian Ni, Sunghee Kim, Reiner Gentz, Ping Feng, Paul A Moore, Steve M Ruben, Ping Wei.
Abstract
DR3 is a death domain-containing receptor that is upregulated during T cell activation and whose overexpression induces apoptosis and NF-kappaB activation in cell lines. Here we show that an endothelial cell-derived TNF-like factor, TL1A, is a ligand for DR3 and decoy receptor TR6/DcR3 and that its expression is inducible by TNF and IL-1alpha. TL1A induces NF-kappaB activation and apoptosis in DR3-expressing cell lines, while TR6-Fc protein antagonizes these signaling events. Interestingly, in T cells, TL1A acts as a costimulator that increases IL-2 responsiveness and secretion of proinflammatory cytokines both in vitro and in vivo. Our data suggest that interaction of TL1A with DR3 promotes T cell expansion during an immune response, whereas TR6 has an opposing effect.Entities:
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Year: 2002 PMID: 11911831 DOI: 10.1016/s1074-7613(02)00283-2
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745