The death receptors Fas and tumor necrosis factor receptor 1 (TNFR1) trigge
r apoptosis upon engagement by their cognate death ligands. Recently, resea
rchers 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 ligan
d binding. Further, mouse gene knockout studies have enabled researchers to
delineate some of the signaling pathways that connect death receptors to t
he cell's apoptotic machinery.