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蛋白磷酸酶2A调节亚基的缺失与应激诱导的心律失常发生率增加有关。

Loss of protein phosphatase 2A regulatory subunit is associated with increased incidence of stress-induced proarrhythmia.

作者信息

Pluteanu Florentina, Glaser Dennis, Massing Fabian, Schulte Jan S, Kirchhefer Uwe

机构信息

Department of Anatomy, Animal Physiology and Biophysics, University of Bucharest, Bucharest, Romania.

Institut für Pharmakologie und Toxikologie, Universitätsklinikum Münster, Universität Münster, Münster, Germany.

出版信息

Front Cardiovasc Med. 2024 May 28;11:1419597. doi: 10.3389/fcvm.2024.1419597. eCollection 2024.

Abstract

BACKGROUND

Protein phosphatase 2A (PP2A) is a serine/threonine-selective holoenzyme that controls Ca homeostasis and contractility of the heart via dephosphorylation of regulatory proteins. In some genetically modified mouse models with increased arrhythmogenicity, a reduced expression of the regulatory subunit B56α of PP2A was found as a concomitant effect. Whether there is a general correlation between the abundance of B56α and the promotion of cardiac arrhythmogenesis remains unclear.

METHODS

The aim of this study was therefore to investigate the role of PP2A-B56α in the propensity for arrhythmic activity in the heart. The experimental analysis of this question has been addressed by using a mouse model with deletion of the PP2A-B56α gene, (KO), in comparison to wild-type animals (WT). Evidence for arrhythmogenicity was investigated in whole animal, isolated heart and cardiomyocytes by ECG, recording of monophasic action potential (MAP) induced by programmed electrical stimulation (PES), measurement of Ca transients under increased pacing frequencies and determination of total K channel currents ( ).

RESULTS

ECG measurements showed a prolongation of QT time in KO vs. WT. KO mice exhibited a higher rate of premature ventricular contractions in the ECG. MAP measurements in Langendorff-perfused KO hearts showed increased episodes of ventricular tachyarrhythmia induced by PES. However, the KO hearts showed values for MAP duration that were similar to those in WT hearts. In contrast, KO showed more myocardial cells with spontaneous arrhythmogenic Ca transient events compared to WT. The whole-cell patch-clamp technique applied to ventricular cardiomyocytes revealed comparable peak potassium channel current densities between KO and WT.

CONCLUSION

These findings support the assumption that a decrease or even the loss of PP2A-B56α leads to an increased propensity of triggered arrhythmias. This could be based on the increased spontaneous Ca tansients observed.

摘要

背景

蛋白磷酸酶2A(PP2A)是一种丝氨酸/苏氨酸选择性全酶,通过对调节蛋白进行去磷酸化来控制心脏的钙稳态和收缩性。在一些致心律失常性增加的基因修饰小鼠模型中,发现PP2A的调节亚基B56α表达降低是伴随效应。B56α的丰度与心脏心律失常发生的促进之间是否存在普遍相关性仍不清楚。

方法

因此,本研究的目的是探讨PP2A-B56α在心脏心律失常活动倾向中的作用。通过使用PP2A-B56α基因缺失的小鼠模型(KO)与野生型动物(WT)进行比较,对这个问题进行了实验分析。通过心电图(ECG)在整体动物、离体心脏和心肌细胞中研究心律失常性的证据,记录程序性电刺激(PES)诱导的单相动作电位(MAP),在增加起搏频率下测量钙瞬变,并测定总钾通道电流( )。

结果

ECG测量显示,与WT相比,KO的QT时间延长。KO小鼠在ECG中表现出更高的室性早搏发生率。在Langendorff灌注的KO心脏中进行的MAP测量显示,PES诱导的室性快速心律失常发作增加。然而,KO心脏的MAP持续时间值与WT心脏相似。相比之下,与WT相比,KO显示出更多具有自发性心律失常性钙瞬变事件的心肌细胞。应用于心室心肌细胞的全细胞膜片钳技术显示,KO和WT之间的峰值钾通道电流密度相当。

结论

这些发现支持以下假设,即PP2A-B56α的减少甚至丧失会导致触发心律失常的倾向增加。这可能基于观察到的自发性钙瞬变增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf69/11165201/f49fef88aa13/fcvm-11-1419597-g001.jpg

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