The mitochondrial permeability transition pore: a mystery solved?

被引:256
作者
Bernardi, Paolo [1 ]
机构
[1] Univ Padua, Dept Biomed Sci, I-35121 Padua, Italy
来源
FRONTIERS IN PHYSIOLOGY | 2013年 / 4卷
关键词
mitochondria; permeability transition; calcium; FoF1 ATP synthase; CA-2&-INDUCED MEMBRANE TRANSITION; ISOLATED LIVER-MITOCHONDRIA; CALCIUM-ION ACCUMULATION; DEPENDENT ANION CHANNEL; RAT-HEART MITOCHONDRIA; MALIC ENZYME-ACTIVITY; CYTOCHROME-C RELEASE; CYCLOSPORINE-A; CYCLOPHILIN-D; CELL-DEATH;
D O I
10.3389/fphys.2013.00095
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The permeability transition (PT) denotes an increase of the mitochondrial inner membrane permeability to solutes with molecular masses up to about 1500 Da. It is presumed to be mediated by opening of a channel, the permeability transition pore (PIP), whose molecular nature remains a mystery. Here I briefly review the history of the PIP discuss existing models, and present our new results indicating that reconstituted dimers of the FOF1 ATP synthase form a channel with properties identical to those of the mitochondrial megachannel (MMC), the electrophysiological equivalent of the PIP Open questions remain, but there is now promise that the PIP can be studied by genetic methods to solve the large number of outstanding problems.
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页数:12
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