The mitochondrial permeability transition from in vitro artifact to disease target

被引:520
作者
Bernardi, P
Krauskopf, A
Basso, E
Petronilli, V
Blalchy-Dyson, E
Di Lisa, F
Forte, MA
机构
[1] Univ Padua, Dept Biomed Sci, I-35121 Padua, Italy
[2] Univ Padua, Inst Neurosci, CNR, I-35121 Padua, Italy
[3] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97201 USA
[4] Univ Padua, Dept Biol Chem, I-35100 Padua, Italy
[5] Univ Padua, CNR, Inst Neurosci, I-35100 Padua, Italy
关键词
apoptosis; calcium; cancer; cell death; degenerative diseases; drugs; mitochondria; necrosis; permeability transition;
D O I
10.1111/j.1742-4658.2006.05213.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mitochondrial permeability transition pore is a high conductance channel whose opening leads to an increase of mitochondrial inner membrane permeability to solutes with molecular masses up to approximate to 1500 Da. In this review we trace the rise of the permeability transition pore from the status of in vitro artifact to that of effector mechanism of cell death. We then cover recent results based on genetic inactivation of putative permeability transition pore components, and discuss their meaning for our understanding of pore structure. Finally, we discuss evidence indicating that the permeability transition pore plays a role in pathophysiology, with specific emphasis on in vivo models of disease.
引用
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页码:2077 / 2099
页数:23
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