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Role of heterogeneity of Kir2.1 channel protein expression in the genesis and stability of cardiac arrhythmias.

机译:Kir2.1通道蛋白表达的异质性在心律不齐的发生和稳定性中的作用。

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摘要

Previous studies have postulated an important role for the inwardly rectifying potassium current (IK1) in controlling the dynamics of electrophysiological spiral waves responsible for ventricular tachycardia and fibrillation. In this study, we developed a novel tissue model of cultured neonatal rat ventricular myocytes (NRVMs) with uniform or heterogeneous Kir2.1 expression achieved by lentiviral transfer to elucidate the role of IK1 in cardiac arrhythmogenesis. Immunohistochemistry, Trypan Blue exclusion, Annexin V binding followed by flow cytometry, and Terminal transferase dUTP Nick End Labeling (TUNEL) assays revealed that lentiviral transduction had no adverse cytotoxic effects on NRVM cultures. Using immunohistochemistry and Western blot, we characterized our cultures for Kir2.1, cardiac troponin I, actin and connexin43 expression levels. Whole-cell patch clamping of Kir2.1-overexpressed NRVMs showed increased IK1 density, hyperpolarized resting membrane potential and increased action potential upstroke velocity compared with GFP-transduced NRVMs. Opposite results were observed in Kir2.1-suppressed NRVMs. Optical mapping of uniformly Kir2.1 gene-modified monolayers showed changes in conduction velocity (CV) and action potential duration (APD) compared with non-transduced and empty vector-transduced monolayers, but functional reentrant waves could not be induced. In monolayers with islands of altered Kir2.1 expression, CV and APD of the transduced and non-transduced regions were similar to those of the uniformly transduced and non-transduced monolayers, respectively. Functional reentrant waves could be induced in monolayers with heterogeneous IK1 expression. The waves were anchored to regions of Kir2.1 overexpression and remained stable, but dropped in frequency and meandered away from regions of Kir2.1 suppression. In monolayers with an inverse pattern of IK1 heterogeneity, stable high frequency spiral waves were present with IK1 overexpression, whereas lower frequency, meandering spiral waves were observed with IK1 suppression. Our study provides direct evidence for the contribution of IK1 heterogeneity to the genesis and stability of spiral waves and highlights the potential importance of IK1 as an anti-arrhythmia target.
机译:先前的研究假设内向整流钾电流(IK1)在控制负责室性心动过速和心律颤动的电生理螺旋波的动力学中起重要作用。在这项研究中,我们开发了一种新型的培养的新生大鼠心室肌细胞(NRVM)组织模型,该蛋白通过慢病毒转移来阐明IK1在心律失常中的作用,具有均匀或异质的Kir2.1表达。免疫组织化学,锥虫蓝排除,膜联蛋白V结合,流式细胞仪和终端转移酶dUTP缺口末端标记(TUNEL)分析表明,慢病毒转导对NRVM培养没有不利的细胞毒性作用。使用免疫组化和蛋白质印迹,我们表征了我们的培养物的Kir2.1,心肌肌钙蛋白I,肌动蛋白和连接蛋白43表达水平。与GFP转导的NRVM相比,Kir2.1过表达的NRVM的全细胞膜片钳夹显示出增加的IK1密度,超极化的静息膜电位和升高的动作电位上风速度。在Kir2.1抑制的NRVM中观察到相反的结果。与未转导和空载体转导的单层相比,均匀地Kir2.1基因修饰的单层的光学作图显示了传导速度(CV)和动作电位持续时间(APD)的变化,但不能诱导功能性折返波。在具有改变的Kir2.1表达的岛的单层中,转导和非转导区域的CV和APD分别类似于均匀转导和非转导的单层的CV和APD。功能性折返波可在具有异质IK1表达的单层中诱导。这些波锚定在Kir2.1过表达区域,并保持稳定,但频率下降,并远离Kir2.1抑制区域。在具有IK1异质性反向模式的单层中,存在IK1过表达的稳定高频螺旋波,而在IK1抑制下观察到较低频率的曲折螺旋波。我们的研究为IK1异质性对螺旋波的发生和稳定性的贡献提供了直接证据,并强调了IK1作为抗心律不齐目标的潜在重要性。

著录项

  • 作者

    Sekar, Rajesh Babu.;

  • 作者单位

    The Johns Hopkins University.;

  • 授予单位 The Johns Hopkins University.;
  • 学科 Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 79 p.
  • 总页数 79
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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