Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.
Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.
Heart Rhythm. 2023 May;20(5):730-736. doi: 10.1016/j.hrthm.2023.01.021. Epub 2023 Jan 21.
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.
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。
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