生物
受体
细胞凋亡
诱饵
程序性细胞死亡
细胞生物学
Fas受体
信号转导
Fas配体
肿瘤坏死因子α
癌症研究
免疫学
遗传学
作者
Avi Ashkenazi,Vishva M. Dixit
标识
DOI:10.1016/s0955-0674(99)80034-9
摘要
The death receptors Fas and tumor necrosis factor receptor 1 (TNFR1) trigger apoptosis upon engagement by their cognate death ligands. Recently, researchers have discovered several novel homologues of Fas and TNFR1: DR 3, 4, 5, and 6 function as death receptors that signal apoptosis, whereas DcR 1, 2, and 3 act as decoys that compete with specific death receptors for ligand binding. Further, mouse gene knockout studies have enabled researchers to delineate some of the signaling pathways that connect death receptors to the cell’s apoptotic machinery.
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