Physical interaction between calcineurin and Cav3.2 T-type Ca2+ channel modulates their functions

被引:17
|
作者
Huang, Ching-Hui [1 ,2 ]
Chen, Yong-Cyuan [2 ]
Chen, Chien-Chang [1 ,2 ]
机构
[1] Natl Def Med Ctr, Grad Inst Life Sci, Taipei 11490, Taiwan
[2] Acad Sinica, Inst Biomed Sci, Taipei 11529, Taiwan
关键词
Calcium channel; Calcineurin; NFAT transcription factor; Cardiac hypertrophy; CARDIAC-HYPERTROPHY; CALCIUM-CHANNELS; ACTIVATION; HEART; PEPTIDE; DOMAINS; COMPLEX; BINDING; CLONING; MEMBER;
D O I
10.1016/j.febslet.2013.04.040
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
Ca(v)3.2 T-type Ca2+ channel is required for the activation of calcineurin/NFAT signaling in cardiac hypertrophy. We aimed to investigate how Ca(v)3.2 and calcineurin interact. We found that Ca2+ and calmodulin modulate the Ca(v)3.2/calcineurin interaction. Calcineurin binding to Ca(v)3.2 decreases the enzyme's phosphatase activity and diminishes the channel's current density. Phenylephrine-induced hypertrophy in neonatal cardiac myocytes is reduced by a cell-permeable peptide with the calcineurin binding site sequence. These data suggest that Ca(v)3.2 regulates calcineurin/NFAT pathway through both the Ca2+ influx and calcineurin binding. Our findings unveiled a reciprocal regulation of Ca2+ signaling which contributes to our understanding of cardiac hypertrophy. Structured summary of protein interactions: Ca(v)3.2 physically interacts with cn by anti tag coimmunoprecipitation (View interaction) (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1723 / 1730
页数:8
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