Independently, production of reactive o ygen spe cies, e. g. by mitochondria or by the NADPH o idase No 1, lipid pero idation, enzymes of the energy meta bolism, the deubiquitinase CYLD and the Bcl 2 family member Bmf have been suggested as further mediators of necroptosis. In addition, our own group has pre viously identified the sphingolipid ceramide as a key effector of TNF induced necroptosis. Moreover, we have been able to show in a very recent study that, in contrast to previous assumptions, TNF induced necroptosis is not mediated by the PARP pathway. Rather, necroptosis induced by TNF and the PARP pathway represent two independent and distinct routes to pro grammed necrosis.

In contrast to apoptosis, which depends essentially on the proteolytic activity of caspases, the role of proteolytic events for both regulation and e ecution of Inhibitors,Modulators,Libraries necroptosis programmed necrosis is considerably less well charac terized. Aside from a negative regulation of necroptosis by caspase 8 via cleavage and inactivation of RIPK1, lysosomal proteases such as cathepsin B, D, calpains, granzymes and cys cathepsins can substitute for caspases in some, but not all forms of programmed necrosis. Also, the endoplasmic reticulum can induce pro grammed necrosis in response to cellular stress or un controlled release of calcium through calpain proteases. Several groups have inde pendently observed that serine protease inhibitors such as tosyl phenylalanyl chloromethyl ketone Inhibitors,Modulators,Libraries can in hibit both necroptosis programmed necrosis and apoptosis. For apoptosis, serine proteases have been found to complement or augment the function of cas pases, e.

g. granzyme B can stimulate apoptosis by cleavage of several procaspases, the pro apoptotic protein Bid, or inhibitor of caspase activated DNAse in cyto to ic T lymphocytes Cilengitide and natural killer cells. For necroptosis programmed necrosis, the identity of the relevant serine proteases and that of their substrates has remained largely obscure. Here, Inhibitors,Modulators,Libraries we have identified the serine protease HtrA2 Omi as a key protease that mediates TNF induced necroptosis. HtrA2 Omi is the mammalian homologue of the bacterial HtrA endoprotease and highly conserved from bacteria to mammalians. In the latter, HtrA2 Omi is involved in the degradation of misfolded proteins during conditions of cellular stress.

Deletion of HtrA2 Omi or mutations affecting its activity have been associated with neuro degeneration and Parkinsons disease in mouse models and patients. In response to apoptotic stimuli, HtrA2 Omi is released from mitochondria into the cyto plasm, where it promotes Inhibitors,Modulators,Libraries apoptosis by binding and inhibiting IAP proteins, thus releasing active caspases from their natural inhibitors. Independently, HtrA2 Omi degrades IAPs, the caspase 8 inhibitor Pea 15 and the anti apoptotic protein HA 1 through its serine protease activity, further promoting apoptosis.