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RIP kinases initiate programmed necrosis Free
Lorenzo Galluzzi1,2,3, Oliver Kepp1,2,3, and Guido Kroemer1,2,3,*
1INSERM, U848, F-94805 Villejuif, France
2Institut Gustave Roussy, F-94805 Villejuif, France
3Université Paris-Sud/Paris XI, F-94270 Le Kremlin Bicêtre, France

*Correspondence to:Guido Kroemer, Tel: +33-1-4211-6046; Fax: +33-1-4211-6047; E-mail: kroemer@orange.fr
J Mol Cell Biol, Volume 1, Issue 1, October 2009, 8-10,  https://doi.org/10.1093/jmcb/mjp007

Some lethal stimuli can induce either apoptosis or necrosis, depending on the cell type and/or experimental setting. Until recently, the molecular bases of this phenomenon were largely unknown. Now, two members of the receptor-interacting serine-threonine kinase (RIP) family, RIP1 and RIP3, have been demonstrated to control the switch between apoptotic and necrotic cell death. Some mechanistic details, however, remain controversial.