RIP kinase-dependent necrosis drives lethal systemic inflammatory response syndrome
Linde Duprez, Nozomi Takahashi, Filip Van Hauwermeiren, Benjamin Vandendriessche, Vera Goossens, Tom Vanden Berghe, Wim Declercq, Claude Libert, Anje Cauwels, Peter Vandenabeele, Linde Duprez, Nozomi Takahashi, Filip Van Hauwermeiren, Benjamin Vandendriessche, Vera Goossens, Tom Vanden Berghe, Wim Declercq, Claude Libert, Anje Cauwels, Peter Vandenabeele
Abstract
Engagement of tumor necrosis factor receptor 1 signals two diametrically opposed pathways: survival-inflammation and cell death. An additional switch decides, depending on the cellular context, between caspase-dependent apoptosis and RIP kinase (RIPK)-mediated necrosis, also termed necroptosis. We explored the contribution of both cell death pathways in TNF-induced systemic inflammatory response syndrome (SIRS). Deletion of apoptotic executioner caspases (caspase-3 or -7) or inflammatory caspase-1 had no impact on lethal SIRS. However, deletion of RIPK3 conferred complete protection against lethal SIRS and reduced the amounts of circulating damage-associated molecular patterns. Pretreatment with the RIPK1 kinase inhibitor, necrostatin-1, provided a similar effect. These results suggest that RIPK1-RIPK3-mediated cellular damage by necrosis drives mortality during TNF-induced SIRS. RIPK3 deficiency also protected against cecal ligation and puncture, underscoring the clinical relevance of RIPK kinase inhibition in sepsis and identifying components of the necroptotic pathway that are potential therapeutic targets for treatment of SIRS and sepsis.
Copyright © 2011 Elsevier Inc. All rights reserved.
Source: PubMed