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miR-448 在缺血和心力衰竭中调节钾电压门控通道亚家族 A 成员 4(KCNA4)。

miR-448 regulates potassium voltage-gated channel subfamily A member 4 (KCNA4) in ischemia and heart failure.

机构信息

Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.

Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.

出版信息

Heart Rhythm. 2023 May;20(5):730-736. doi: 10.1016/j.hrthm.2023.01.021. Epub 2023 Jan 21.


DOI:10.1016/j.hrthm.2023.01.021
PMID:36693615
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10149585/
Abstract

BACKGROUND: MicroRNA miR-448 mediates some of the effects of ischemia on arrhythmic risk. Potassium voltage-gated channel subfamily A member 4 (KCNA4) encodes a K1.4 current that opens in response to membrane depolarization and is essential for regulating the action potential duration in heart. KCNA4 has a miR-448 binding site. OBJECTIVE: We investigated whether miR-448 was involved in the regulation of KCNA4 messenger RNA expression in ischemia. METHODS: Quantitative real-time reverse-transcriptase polymerase chain reaction was used to investigate the expression of KCNA4 and miR-448. Pull-down assays were used to examine the interaction between miR-448 and KCNA4. miR-448 decoy and binding site mutation were used to examine the specificity of the effect for KCNA4. RESULTS: The expression of KCNA4 is diminished in ischemia and human heart failure tissues with ventricular tachycardia. Previously, we have shown that miR-448 is upregulated in ischemia and inhibition can prevent arrhythmic risk after myocardial infarction. The 3'-untranslated region of KCNA4 has a conserved miR-448 binding site. miR-448 bound to this site directly and reduced KCNA4 expression and the transient outward potassium current. Inhibition of miR-448 restored KCNA4. CONCLUSION: These findings showed a link between K1.4 downregulation and miR-448-mediated upregulation in ischemia, suggesting a new mechanism for the antiarrhythmic effect of miR-448 inhibition.

摘要

背景:微小 RNA miR-448 介导了部分缺血对心律失常风险的影响。钾电压门控通道亚家族 A 成员 4(KCNA4)编码 K1.4 电流,该电流在膜去极化时开放,对心脏动作电位持续时间的调节至关重要。KCNA4 有一个 miR-448 结合位点。

目的:我们研究了 miR-448 是否参与了缺血对 KCNA4 信使 RNA 表达的调节。

方法:采用实时定量逆转录聚合酶链反应检测 KCNA4 和 miR-448 的表达。采用下拉实验检测 miR-448 与 KCNA4 的相互作用。采用 miR-448 诱饵和结合位点突变来检验对 KCNA4 的作用的特异性。

结果:在缺血和伴有室性心动过速的人心力衰竭组织中,KCNA4 的表达减少。之前,我们已经表明 miR-448 在缺血时上调,抑制 miR-448 可以预防心肌梗死后的心律失常风险。KCNA4 的 3'非翻译区有一个保守的 miR-448 结合位点。miR-448 直接结合这个位点,减少 KCNA4 的表达和瞬时外向钾电流。抑制 miR-448 恢复了 KCNA4。

结论:这些发现表明,在缺血中,K1.4 下调与 miR-448 介导的上调之间存在联系,提示 miR-448 抑制的抗心律失常作用有一个新的机制。

相似文献

[1]
miR-448 regulates potassium voltage-gated channel subfamily A member 4 (KCNA4) in ischemia and heart failure.

Heart Rhythm. 2023-5

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
Molecular basis of transient outward potassium current downregulation in human heart failure: a decrease in Kv4.3 mRNA correlates with a reduction in current density.

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引用本文的文献

[1]
Mitochondrial dysfunction as a central hub linking Na/Ca homeostasis and inflammation in ischemic arrhythmias: therapeutic implications.

Front Cardiovasc Med. 2025-8-12

[2]
The Role of Infarct Border Zone Remodelling in Ventricular Arrhythmias: Bridging Basic Research and Clinical Applications.

J Cell Mol Med. 2025-4

[3]
Study on Potential Differentially Expressed Genes in Idiopathic Pulmonary Fibrosis by Bioinformatics and Next-Generation Sequencing Data Analysis.

Biomedicines. 2023-11-21

[4]
MicroRNAs: Midfielders of Cardiac Health, Disease and Treatment.

Int J Mol Sci. 2023-11-11

本文引用的文献

[1]
Three-Week-Old Rabbit Ventricular Cardiomyocytes as a Novel System to Study Cardiac Excitation and EC Coupling.

Front Physiol. 2021-11-18

[2]
Nucleoporin 50 mediates Kcna4 transcription to regulate cardiac electrical activity.

J Cell Sci. 2021-9-15

[3]
Inhibition of the unfolded protein response reduces arrhythmia risk after myocardial infarction.

J Clin Invest. 2021-9-15

[4]
Voltage-gated potassium channel dysfunction in dorsal root ganglia contributes to the exaggerated exercise pressor reflex in rats with chronic heart failure.

Am J Physiol Heart Circ Physiol. 2021-8-1

[5]
MIR448 antagomir reduces arrhythmic risk after myocardial infarction by upregulating the cardiac sodium channel.

JCI Insight. 2020-12-3

[6]
Fluconazole Represses Cytochrome P450 1B1 and Its Associated Arachidonic Acid Metabolites in the Heart and Protects Against Angiotensin II-Induced Cardiac Hypertrophy.

J Pharm Sci. 2020-7

[7]
Development of endomyocardial fibrosis model using a cell patterning technique: In vitro interaction of cell coculture of 3T3 fibroblasts and RL-14 cardiomyocytes.

PLoS One. 2020-2-24

[8]
Sudden Cardiac Death in Ischemic Heart Disease: From Imaging Arrhythmogenic Substrate to Guiding Therapies.

JACC Cardiovasc Imaging. 2020-10

[9]
Metabolic regulation of Kv channels and cardiac repolarization by Kvβ2 subunits.

J Mol Cell Cardiol. 2019-10-19

[10]
miRWalk: An online resource for prediction of microRNA binding sites.

PLoS One. 2018-10-18

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