ps1145 and Hepatitis

Tumor necrosis factor (TNF) is a key signaling molecule orchestrating immune and inflammatory responses and possesses the capacity to trigger apoptotic as well as necroptotic cell death. Apoptotic cell death elicited by TNF has been demonstrated to engage pro-apoptotic Bcl-2 family proteins, most prominently the BH3-only protein Bid, a key substrate of caspase-8, the key effector protease downstream of TNF receptor I. Most recently, the BH3 domain-containing protein Bad (Bcl-2-antagonist of cell death) has been shown to be rate limiting for TNF-mediated cell death, suggesting possible synergy with Bid, but genetic analyses presented here demonstrate that it is dispensable for this process.

Topics: Animals; bcl-Associated Death Protein; Cell Death; Embryo, Mammalian; Fibroblasts; Hepatitis; Heterocyclic Compounds, 3-Ring; Humans; I-kappa B Kinase; Mice, Inbred C57BL; Pyridines; Thymocytes; Tumor Necrosis Factor-alpha