CKIP-1 介导 CK2 转位以调节心肌细胞中的 Nav1.5 和 Kir2.1 通道复合物。

IF 3.2 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xinran Li, Yingzhu Zhao, Mei Xue, Hesheng Hu, Jie Yin, Wenjuan Cheng, Yugen Shi, Ye Wang, Suhua Yan
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引用次数: 0

摘要

钠和钾通道,尤其是 Nav1.5 和 Kir2.1,在心肌细胞动作电位的形成过程中发挥着关键作用。这些通道与突触相关蛋白 97(SAP97)相互作用并受其调控。然而,SAP97 在心肌细胞中的调控作用仍不完全清楚。在此,我们研究了 SAP97 磷酸化在调控 Nav1.5 和 Kir2.1 通道复合物中的功能以及 SAP97 的上游调控。我们发现 SAP97 在体外被酪蛋白激酶 II(CK2)磷酸化。此外,将酪蛋白激酶 2 交互蛋白-1(CKIP-1)转染到心肌细胞,使 CK2 从细胞核转移到细胞质,可增加 SAP97 磷酸化及 Nav1.5 和 Kir2.1 电流活性。这些研究结果表明,CKIP-1 可调节 CK2 的亚细胞转位,而 CK2 可调节心肌细胞中 Nav1.5 和 Kir2.1 通道复合物的形成和活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CKIP-1 mediates CK2 translocation to regulate Nav1.5 and Kir2.1 channel complexes in cardiomyocytes

CKIP-1 mediates CK2 translocation to regulate Nav1.5 and Kir2.1 channel complexes in cardiomyocytes

Sodium and potassium channels, especially Nav1.5 and Kir2.1, play key roles in the formation of action potentials in cardiomyocytes. These channels interact with, and are regulated by, synapse-associated protein 97 (SAP97). However, the regulatory role of SAP97 in myocyte remains incompletely understood. Here, we investigate the function of SAP97 phosphorylation in the regulation of Nav1.5 and Kir2.1 channel complexes and the upstream regulation of SAP97. We found that SAP97 is phosphorylated by casein kinase II (CK2) in vitro. In addition, transfection of casein kinase 2 interacting protein-1 (CKIP-1) into cardiomyocytes to drive CK2 from the nucleus to the cytoplasm, increased SAP97 phosphorylation and Nav1.5 and Kir2.1 current activity. These findings demonstrated that CKIP-1 modulates the subcellular translocation of CK2, which regulates Nav1.5 and Kir2.1 channel complex formation and activity in cardiomyocytes.

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来源期刊
CiteScore
5.80
自引率
2.80%
发文量
277
审稿时长
6-12 weeks
期刊介绍: The Journal of Biochemical and Molecular Toxicology is an international journal that contains original research papers, rapid communications, mini-reviews, and book reviews, all focusing on the molecular mechanisms of action and detoxication of exogenous and endogenous chemicals and toxic agents. The scope includes effects on the organism at all stages of development, on organ systems, tissues, and cells as well as on enzymes, receptors, hormones, and genes. The biochemical and molecular aspects of uptake, transport, storage, excretion, lactivation and detoxication of drugs, agricultural, industrial and environmental chemicals, natural products and food additives are all subjects suitable for publication. Of particular interest are aspects of molecular biology related to biochemical toxicology. These include studies of the expression of genes related to detoxication and activation enzymes, toxicants with modes of action involving effects on nucleic acids, gene expression and protein synthesis, and the toxicity of products derived from biotechnology.
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