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Compartmentalized cAMP signalling is important in the regulation of Ca(2+) cycling in the heart.

作者信息

Lygren B, Taskén K

机构信息

Biotechnology Centre of Oslo, University of Oslo, PO Box 1125 Blindern, N-0317 Oslo, Norway.

出版信息

Biochem Soc Trans. 2006 Aug;34(Pt 4):489-91. doi: 10.1042/BST0340489.

DOI:10.1042/BST0340489
PMID:16856840
Abstract

Co-ordinated myocyte handling of calcium is essential for efficient excitation-contraction coupling in the heart. The calcium cycling activity can be modulated by adrenergic stimulation and subsequent phosphorylation. Important functional consequences of phosphorylation include a greater influx of calcium through the voltage-dependent L-type Ca(2+) channel and a greater release of calcium from SR (sarcoplasmic reticulum) through the ryanodine R2 receptor. Furthermore, a more efficient reuptake through SERCA2 (sarcoplasmic/endoplasmic-reticulum Ca(2+)-ATPase 2) is a result of phosphorylation of its regulatory protein phospholamban. Compartmentalized signalling is important in this signalling cascade, and A-kinase-anchoring proteins play a central role by providing a high level of specificity.

摘要

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