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