4.8 Review

Necroptosis and its role in inflammation

Journal

NATURE
Volume 517, Issue 7534, Pages 311-320

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nature14191

Keywords

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Funding

  1. European Research Council [2012-ADG_20120314]
  2. German Research Foundation [SFB670, SFB829, SPP1656]
  3. European Commission [223404, 223151]
  4. Deutsche Krebshilfe
  5. Else Kroner-Fresenius-Stiftung
  6. Helmholtz Alliance (PCCC)
  7. Belgian grants (Interuniversity Attraction Poles) [IAP 7/32]
  8. Flemish grants (Research Foundation Flanders) [FWO G.0875.11, FWO G.0973.11 N, FWO G.0A45.12 N, FWO G.0172.12, FWO G.0787.13N, G0C3114N, FWO KAN 31528711, 2012-188]
  9. Gent University grants (MRP, GROUP-ID consortium)
  10. Flanders Institute for Biotechnology (VIB)
  11. Flemish Government [B0F09/01M00709]

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Regulated cell death has essential functions in development and in adult tissue homeostasis. Necroptosis is a newly discovered pathway of regulated necrosis that requires the proteins RIPK3 and MLKL and is induced by death receptors, interferons, toll-like receptors, intracellular RNA and DNA sensors, and probably other mediators. RIPK1 has important kinase-dependent and scaffolding functions that inhibit or trigger necroptosis and apoptosis. Mouse-model studies have revealed important functions for necroptosis in inflammation and suggested that it could be implicated in the pathogenesis of many human inflammatory diseases. We discuss the mechanisms regulating necroptosis and its potential role in inflammation and disease.

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