The sarcoplasmic reticulum luminal thiol oxidase ERO1 regulates cardiomyocyte excitation-coupled calcium release and response to hemodynamic load

被引:49
作者
Chin, King-Tung [2 ]
Kang, Guoxin [1 ]
Qu, Jiaxiang
Gardner, Lawrence B.
Coetzee, William A. [4 ]
Zito, Ester [2 ]
Fishman, Glenn I.
Ron, David [2 ,3 ,5 ]
机构
[1] NYU, Sch Med, Leon H Charney Div Cardiol, Dept Med, New York, NY 10016 USA
[2] NYU, Sch Med, Kimmel Ctr Biol & Med, Skirball Inst, New York, NY 10016 USA
[3] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
[4] NYU, Sch Med, Dept Pediat, New York, NY 10016 USA
[5] Univ Cambridge, Inst Metab Sci, Cambridge, England
基金
美国国家卫生研究院;
关键词
disulfide bonds; endoplasmic reticulum; heart failure; OXIDATIVE STRESS; PROTEIN; GENE; HOMEOSTASIS; MECHANISMS; PATHWAYS; HYPOXIA; CELLS; HEART; SERCA;
D O I
10.1096/fj.11-184622
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Two related ER oxidation 1 (ERO1) proteins, ERO1 alpha and ERO1 beta, dynamically regulate the redox environment in the mammalian endoplasmic reticulum (ER). Redox changes in cysteine residues on intralumenal loops of calcium release and reuptake channels have been implicated in altered calcium release and reuptake. These findings led us to hypothesize that altered ERO1 activity may affect cardiac functions that are dependent on intracellular calcium flux. We established mouse lines with loss of function insertion mutations in Ero1l and Ero1lb encoding ERO1 alpha and ERO1 beta. The peak amplitude of calcium transients in homozygous Ero1 alpha mutant adult cardiomyocytes was reduced to 42.0 +/- 2.2% (n = 10, P <= 0.01) of values recorded in wild-type cardiomyocytes. Decreased ERO1 activity blunted cardiomyocyte inotropic response to adrenergic stimulation and sensitized mice to adrenergic blockade. Whereas all 12 wild-type mice survived challenge with 4 mg/kg esmolol, 6 of 8 compound Ero1l and Ero1lb mutant mice succumbed to this level of beta adrenergic blockade (P <= 0.01). In addition, mice lacking ERO1 alpha were partially protected against progressive heart failure in a transaortic constriction model [at 10 wk postprocedure, fractional shortening was 0.31 +/- 0.02 in the mutant (n = 20) vs. 0.23 +/- 0.03 in the wild type (n = 18); P <= 0.01]. These findings establish a role for ERO1 in calcium homeostasis and suggest that modifying the lumenal redox environment may affect the progression of heart failure.Chin, K. T., Kang, G., Qu, J., Gardner, L. B., Coetzee, W. A., Zito, E., Fishman, G. I., Ron, R. The sarcoplasmic reticulum luminal thiol oxidase ERO1 regulates cardiomyocyte excitation-coupled calcium release and response to hemodynamic load. FASEB J. 25, 2583-2591 (2011). www.fasebj.org
引用
收藏
页码:2583 / 2591
页数:9
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