Regulation of the ryanodine receptor in heart failure

被引:0
|
作者
Steven O. Marx
Andrew R. Marks
机构
[1] Center for Molecular Cardiology,
[2] Division of Cardiology,undefined
[3] Departments of Medicine and Pharmacology,undefined
[4] Columbia University College of Physicians,undefined
[5] and Surgeons,undefined
[6] Rm 9-401,undefined
[7] 630 West 168th Street,undefined
[8] New York,undefined
[9] NY 10032,undefined
[10] USA,undefined
[11] Tel.: +1-212/305-0270,undefined
[12] Fax: +1-212/305-3690,undefined
[13] E-Mail: arm42@columbia.edu,undefined
关键词
Key words Ryanodine receptor – calcium – heart failure – ion channel – phosphorylation;
D O I
10.1007/s003950200029
中图分类号
学科分类号
摘要
In the heart, calcium (Ca2+) regulates muscle contraction and electrical signals that determine cardiac rhythm and cell growth pathways. The ryanodine receptor (RyR), an intracellular Ca2+ release channel, is required for excitation-contraction coupling. The cardiac RyR has a large cytoplasmic structure that serves as a scaffold for modulatory proteins that regulate the function of the channel. Protein kinase A (PKA) phosphorylation of RyR2 dissociates the regulatory protein FKBP 12.6 and regulates the open probability of the channel. In failing hearts, RyR2 is PKA hyperphosphorylated resulting in defective channel function due to increased sensitivity to Ca2+ induced activation.
引用
收藏
页码:I49 / I51
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