Mitochondrial Ca2+ transport and permeability transition in zebrafish (Danio rerio)

被引:30
作者
Azzolin, Luca [1 ,2 ]
Basso, Emy [1 ,2 ]
Argenton, Francesco [3 ]
Bernardi, Paolo [1 ,2 ,4 ]
机构
[1] Univ Padua, Dept Biomed Sci, I-35121 Padua, Italy
[2] Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy
[3] Univ Padua, Dept Biol, I-35121 Padua, Italy
[4] Venetian Inst Mol Med, Padua, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2010年 / 1797卷 / 11期
关键词
Mitochondria; Permeability Transition; Cyclosporin A; Disease models; Drug screening; RAT-LIVER MITOCHONDRIA; CYCLOSPORINE-A; CYCLOPHILIN-D; CELL-DEATH; UBIQUINONE ANALOGS; HEART-MITOCHONDRIA; MUSCLE APOPTOSIS; OXIDATIVE STRESS; SKELETAL-MUSCLE; MYOPATHIC MICE;
D O I
10.1016/j.bbabio.2010.07.002
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
We have studied mitochondrial Ca2+ transport and the permeability transition (PT) in the teleost zebrafish (Danio rerio), a key model system for human diseases. Permeabilized zebrafish embryo cells displayed a mitochondria! energy-dependent Ca2+ uptake system that, like the Ca2+ uniporter of mammals, was inhibited by ruthenium red. Zebrafish mitochondria underwent a Ca2+-dependent PT that displayed Pi-dependent desensitization by cyclosporin A, and responded appropriately to key modulators of the mammalian PT pore (voltage, pH, ubiquinone 0, dithiol oxidants and cross linkers, ligands of the adenine nucleotide translocator, arachidonic acid). Opening of the pore was documented in intact cells, where it led to death that could largely be prevented by cyclosporin A. Our results represent a necessary step toward the use of zebrafish for the screening and validation of PTP inhibitors of potential use in human diseases, as recently shown for collagen VI muscular dystrophy [Telfer et al., 2010]. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1775 / 1779
页数:5
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