4.7 Article

Necroptosis, necrosis and secondary necrosis converge on similar cellular disintegration features

期刊

CELL DEATH AND DIFFERENTIATION
卷 17, 期 6, 页码 922-930

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/cdd.2009.184

关键词

necrosis; time-lapse; RIP1; Fenton reactions; lysosomes

资金

  1. Flanders Institute for Biotechnology (VIB)
  2. FWO (Fonds Wetenschappelijk Onderzoek Vlaanderen)
  3. BOF, Ghent University
  4. Flemish Government
  5. European Union [MRTN-CT-035624]
  6. EC [LSHB-CT-2005-019067, HEALTH-F4-2007-200767)]
  7. Fonds voor Wetenschappelijk Onderzoek - Vlaanderen [G.0133.05, 3G.0218.06]
  8. Ghent University

向作者/读者索取更多资源

Necroptosis, necrosis and secondary necrosis following apoptosis represent different modes of cell death that eventually result in similar cellular morphology including rounding of the cell, cytoplasmic swelling, rupture of the plasma membrane and spilling of the intracellular content. Subcellular events during tumor necrosis factor (TNF)-induced necroptosis, H(2)O(2)-induced necrosis and anti-Fas-induced secondary necrosis were studied using high-resolution time-lapse microscopy. The cellular disintegration phase of the three types of necrosis is characterized by an identical sequence of subcellular events, including oxidative burst, mitochondrial membrane hyperpolarization, lysosomal membrane permeabilization and plasma membrane permeabilization, although with different kinetics. H(2)O(2)-induced necrosis starts immediately by lysosomal permeabilization. In contrast, during TNF-mediated necroptosis and anti-Fas-induced secondary necrosis, this is a late event preceded by a defined signaling phase. TNF-induced necroptosis depends on receptor-interacting protein-1 kinase, mitochondrial complex I and cytosolic phospholipase A(2) activities, whereas H(2)O(2)-induced necrosis requires iron-dependent Fenton reactions.

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