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组织特异性肾上腺素调节 L 型钙通道 Ca1.2。

Tissue-specific adrenergic regulation of the L-type Ca channel Ca1.2.

机构信息

Department of Pharmacology, University of California, Davis, Davis, CA 95616, USA.

出版信息

Sci Signal. 2020 Dec 22;13(663):eabc6438. doi: 10.1126/scisignal.abc6438.

DOI:10.1126/scisignal.abc6438
PMID:33443233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7909005/
Abstract

Ca influx through the L-type Ca channel Cav1.2 triggers each heartbeat. The fight-or-flight response induces the release of the stress response hormone norepinephrine to stimulate β-adrenergic receptors, cAMP production, and protein kinase A activity to augment Ca influx through Ca1.2 and, consequently, cardiomyocyte contractility. Emerging evidence shows that Ca1.2 is regulated by different mechanisms in cardiomyocytes compared to neurons and vascular smooth muscle cells.

摘要

钙离子通过 L 型钙通道 Cav1.2 流入引发每次心跳。战斗或逃跑反应会诱导应激反应激素去甲肾上腺素的释放,以刺激β肾上腺素能受体、cAMP 的产生和蛋白激酶 A 的活性,从而增强钙离子通过 Ca1.2 的流入,进而增强心肌细胞的收缩力。新出现的证据表明,与神经元和血管平滑肌细胞相比,心肌细胞中 Ca1.2 的调节机制不同。

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Circ Res. 2021 Jan 8;128(1):76-88. doi: 10.1161/CIRCRESAHA.120.317839. Epub 2020 Oct 22.
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α-Actinin-1 promotes activity of the L-type Ca channel Ca 1.2.α-辅肌动蛋白-1 促进 L 型钙通道 Ca 1.2 的活性。
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β-Adrenergic Stimulation Compartmentalizes β Signaling Into Nanoscale Local Domains by Targeting the C-Terminus of β-Adrenoceptors.β-肾上腺素能刺激通过靶向β肾上腺素受体的 C 末端将β信号分隔到纳米级局部域中。
Circ Res. 2019 Apr 26;124(9):1350-1359. doi: 10.1161/CIRCRESAHA.118.314322.
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A G-coupled purinergic receptor boosts Ca influx and vascular contractility during diabetic hyperglycemia.G 蛋白偶联嘌呤能受体在糖尿病高血糖期间增强钙内流和血管收缩性。
Elife. 2019 Mar 1;8:e42214. doi: 10.7554/eLife.42214.
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Cardiac CaV1.2 channels require β subunits for β-adrenergic-mediated modulation but not trafficking.心肌 CaV1.2 通道需要β亚基来进行β肾上腺素能介导的调节,但不需要运输。
J Clin Invest. 2019 Feb 1;129(2):647-658. doi: 10.1172/JCI123878. Epub 2019 Jan 7.
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Functionally distinct and selectively phosphorylated GPCR subpopulations co-exist in a single cell.功能不同且选择性磷酸化的 G 蛋白偶联受体亚群存在于单个细胞中。
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