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.
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.
We investigated whether miR-448 was involved in the regulation of KCNA4 messenger RNA expression in ischemia.
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.
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.
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.
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。
我们研究了 miR-448 是否参与了缺血对 KCNA4 信使 RNA 表达的调节。
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。
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。
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。