cIAPs Block Ripoptosome Formation, a RIP1/Caspase-8 Containing Intracellular Cell Death Complex Differentially Regulated by cFLIP Isoforms
Heidelberg University · University Hospital Heidelberg · +5 more institutions
Abstract
The intracellular regulation of cell death pathways by cIAPs has been enigmatic. Here we show that loss of cIAPs promotes the spontaneous formation of an intracellular platform that activates either apoptosis or necroptosis. This 2 MDa intracellular complex that we designate "Ripoptosome" is necessary but not sufficient for cell death. It contains RIP1, FADD, caspase-8, caspase-10, and caspase inhibitor cFLIP isoforms. cFLIP(L) prevents Ripoptosome formation, whereas, intriguingly, cFLIP(S) promotes Ripoptosome assembly. When cIAPs are absent, caspase activity is the "rheostat" that is controlled by cFLIP isoforms in the Ripoptosome and decides if cell death occurs by RIP3-dependent necroptosis or…
Citation impact
- FWCI
- 34.98
- Percentile
- 100%
- References
- 60
Authors
10- MFMaria Feoktistova
Heidelberg University, University Hospital Heidelberg, University Medical Centre Mannheim, Otto-von-Guericke-Universität Magdeburg
- PGPeter Geserick
Heidelberg University, University Hospital Heidelberg, University Medical Centre Mannheim, Otto-von-Guericke-Universität Magdeburg
- BKBeate Kellert
Heidelberg University, University Hospital Heidelberg, University Medical Centre Mannheim
- DPDiana Panayotova Dimitrova
Heidelberg University, University Hospital Heidelberg, University Medical Centre Mannheim
- CLClaudia Langlais
University of Leicester, MRC Toxicology Unit
Topics & keywords
- Necroptosis
- FADD
- Biology
- Cell biology
- Intracellular
- Programmed cell death
- Caspase 8
- TRADD
- Good health and well-being