Voltage-dependent anion channel involved in the mitochondrial calcium cycle of cell lines carrying the mitochondrial DNA A4263G mutation

被引:11
作者
Liu, Yuqi [1 ]
Gao, Lei [1 ]
Xue, Qiao [1 ]
Li, Zongbin [1 ]
Wang, Lin [1 ]
Chen, Rui [1 ]
Liu, Mohan [1 ]
Wen, Yi [1 ]
Guan, Minxin [2 ]
Li, Yang [1 ]
Wang, Shiwen [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Inst Geriatr Cardiol, Beijing 100853, Peoples R China
[2] Cincinnati Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
关键词
Mitochondrial DNA (mtDNA); VDAC; Mitochondrial calcium cycle; Mitochondrial membrane potential; MATERNALLY INHERITED HYPERTENSION; PERMEABILITY TRANSITION; CARDIAC MYOCYTES; CYTOCHROME-C; INHIBITION; COMPLEXES; MECHANISM; RELEASE; DEATH;
D O I
10.1016/j.bbrc.2010.11.124
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
In this study, we investigated the effects of the voltage-dependent anion channel (VDAC) on the mitochondrial calcium cycle in cell lines carrying the mitochondrial DNA A4263G mutation. We established lymphoblastoid cell lines from three symptomatic individuals and one asymptomatic individual from the large Chinese Han family carrying the A4263G mutation; these were compared with three control cell lines. The mitochondrial Ca2+ concentration and membrane potential were detected by loading cells with Rhod-2 and JC-1, respectively. Confocal imagines showed the average Rhod-2 and JC-1 fluorescence levels of individuals carrying the tRNA(Ile) A4263G mutation were lower than those of the control group (P < 0.05). The baseline Rhod-2 fluorescence in the control group increased after exposure to atractyloside (an opener of the adenine nucleotide translocator, P < 0.05), but no significant change was detected in the cell line harboring the A4263G mutation (P > 0.05). The baseline JC-1 fluorescence in both the mutated and control cell lines decreased after subsequent exposure to atractyloside (P < 0.05), whereas this effect of atractyloside was inhibited by Cyclosporin A (CsA, a VDAC blocker). We conclude that the mitochondrial VDAC is involved in both the increase of mitochondrial permeability to Ca2+ and the decrease of mitochondrial membrane potential in cell lines carrying the mtDNA A4263G mutation. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:364 / 369
页数:6
相关论文
共 18 条
  • [1] Complexes between kinases, mitochondrial porin and adenylate translocator in rat brain resemble the permeability transition pore
    Beutner, G
    Ruck, A
    Riede, B
    Welte, W
    Brdiczka, D
    [J]. FEBS LETTERS, 1996, 396 (2-3) : 189 - 195
  • [2] Mitochondrial ADP/ATP carrier can be reversibly converted into a large channel by Ca2+
    Brustovetsky, N
    Klingenberg, M
    [J]. BIOCHEMISTRY, 1996, 35 (26) : 8483 - 8488
  • [3] Mitochondrial intermembrane junctional complexes and their involvement in cell death
    Crompton, M
    Barksby, E
    Johnson, N
    Capano, M
    [J]. BIOCHIMIE, 2002, 84 (2-3) : 143 - 152
  • [4] Calcium binding and translocation by the voltage-dependent anion channel: a possible regulatory mechanism in mitochondrial function
    Gincel, D
    Zaid, H
    Shoshan-Barmatz, V
    [J]. BIOCHEMICAL JOURNAL, 2001, 358 (358) : 147 - 155
  • [5] Prevalence, awareness, treatment, and control of hypertension in China
    Gu, DF
    Reynolds, K
    Wu, XG
    Chen, J
    Duan, XF
    Muntner, P
    Huang, GY
    Reynolds, RF
    Su, SY
    Whelton, PK
    He, J
    [J]. HYPERTENSION, 2002, 40 (06) : 920 - 927
  • [6] Mitochondrial calcium transport: mechanisms and functions
    Gunter, TE
    Buntinas, L
    Sparagna, G
    Eliseev, R
    Gunter, K
    [J]. CELL CALCIUM, 2000, 28 (5-6) : 285 - 296
  • [7] Opening of mitochondrial KATP channels attenuates the ouabain-induced calcium overload in mitochondria
    Ishida, H
    Hirota, Y
    Genka, C
    Nakazawa, H
    Nakaya, H
    Sato, T
    [J]. CIRCULATION RESEARCH, 2001, 89 (10) : 856 - 858
  • [8] The relationship between mitochondrial state, ATP hydrolysis, [Mg2+], and [Ca2+](i) studied in isolated rat cardiomyocytes
    Leyssens, A
    Nowicky, AV
    Patterson, L
    Crompton, M
    Duchen, MR
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1996, 496 (01): : 111 - 128
  • [9] Failures in Mitochondrial tRNAMet and tRNAGln Metabolism Caused by the Novel 4401A&gt;G Mutation Are Involved in Essential Hypertension in a Han Chinese Family
    Li, Ronghua
    Liu, Yuqi
    Li, Zongbin
    Yang, Li
    Wang, Shiwen
    Guan, Min-Xin
    [J]. HYPERTENSION, 2009, 54 (02) : 329 - 337
  • [10] Maternally inherited hypertension is associated with the mitochondrial tRNAIle A4295G mutation in a Chinese family
    Li, Zongbin
    Liu, Yuqi
    Yang, Li
    Wang, Shwen
    Guan, Min-Xin
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 367 (04) : 906 - 911