Identity, structure, and function of the mitochondrial permeability transition pore: controversies, consensus, recent advances, and future directions
University of Padua · Protein Research Foundation · +10 more institutions
Abstract
Abstract The mitochondrial permeability transition (mPT) describes a Ca 2+ -dependent and cyclophilin D (CypD)-facilitated increase of inner mitochondrial membrane permeability that allows diffusion of molecules up to 1.5 kDa in size. It is mediated by a non-selective channel, the mitochondrial permeability transition pore (mPTP). Sustained mPTP opening causes mitochondrial swelling, which ruptures the outer mitochondrial membrane leading to subsequent apoptotic and necrotic cell death, and is implicated in a range of pathologies. However, transient mPTP opening at various sub-conductance states may contribute several physiological roles such as alterations in mitochondrial bioenergetics and rapid Ca 2+…
Citation impact
- FWCI
- 54.62
- Percentile
- 100%
- References
- 283
Authors
9Topics & keywords
- Mitochondrial permeability transition pore
- Permeability (electromagnetism)
- Function (biology)
- Identity (music)
- Chemistry
- Biophysics
- Computational biology
- Cell biology
Funding
- JAJapan Agency for Medical Research and DevelopmentAwards: JP22ama121001j0001, JP16K07266, 17H03647, JP 17H03647
- FLFondation LeducqAwards: 16CVD04, GGP17092
- MOMinistry of Education, Culture, Sports, Science and TechnologyAward: JP 17H03647
- AIAssociazione Italiana per la Ricerca sul CancroAward: IG23129
- AAIRIcercaAward: IG23129
- NINational Institutes of HealthAwards: R37NS045876, R01HL122124, R01HL142864, R35GM139615, R01HL093671, R01AG058256, RF1AG072484, K01AG054734, R01HL137266
- NINational Institute on AgingAwards: R56AG078384, R01AG058256, RF1AG072484, 7K01AG054734, K01AG054734
- NHNational Heart, Lung, and Blood InstituteAwards: 5 R01 HL093671, R01HL122124, R01HL137266, HL150031, R01HL142864, R01HL093671
- NINational Institute of General Medical SciencesAward: R35GM139615
- NINational Institute of Neurological Disorders and StrokeAward: 2R37NS045876-18
- COCenter of Innovation ProgramAward: JP 17H03647