Calcium signaling dysfunction in heart disease

被引:12
作者
Cartwright, Elizabeth J. [1 ]
Mohamed, Tamer [1 ]
Oceandy, Delvac [1 ]
Neyses, Ludwig [1 ]
机构
[1] Univ Manchester, Manchester Acad Hlth Sci Ctr, Cardiovasc Med Res Grp, Manchester M13 9PT, Lancs, England
基金
英国医学研究理事会;
关键词
calcium signaling; cardiac hypertrophy; heart failure; genetically encoded calcium indicators; NITRIC-OXIDE SYNTHASE; GREEN FLUORESCENT PROTEINS; MEMBRANE CA2+ ATPASE; PLASMA-MEMBRANE; ENDOPLASMIC-RETICULUM; CARDIAC-HYPERTROPHY; IN-VIVO; INOSITOL TRISPHOSPHATE; PUMP; CA2+-ATPASE;
D O I
10.1002/biof.149
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 the heart, Ca2+ is crucial for the regulation of contraction and intracellular signaling, processes, which are vital to the functioning of the healthy heart. Ca2+-activated signaling pathways must function against a background of large, rapid, and tightly regulated changes in intracellular free Ca2+ concentrations during each contraction and relaxation cycle. This review highlights a number of proteins that regulate signaling Ca2+ in both normal and pathological conditions including cardiac hypertrophy and heart failure, and discusses how these pathways are not regulated by the marked elevation in free intracellular calcium ([Ca2+](i)) during contraction but require smaller sustained increases in Ca2+ concentration. In addition, we present published evidence that the pool of Ca2+ that regulates signaling is compartmentalized into distinct cellular microdomains and is thus distinct from that regulating contraction. (C) 2011 International Union of Biochemistry and Molecular Biology, Inc.
引用
收藏
页码:175 / 181
页数:7
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