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首页> 外文期刊>Experimental and therapeutic medicine >Function of a novel plakophilin-2 mutation in the abnormal expression of connexin43 in a patient with arrhythmogenic right ventricular cardiomyopathy
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Function of a novel plakophilin-2 mutation in the abnormal expression of connexin43 in a patient with arrhythmogenic right ventricular cardiomyopathy

机译:新的plakophilin-2突变在心律失常性右室心肌病患者中connexin43异常表达中的作用

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摘要

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a desmosomal disease. Desmosomes and gap junctions are important structural components of cardiac intercalated discs. The proteins plakophilin-2 (PKP-2) and connexin43 (Cx43) are components of desmosomes and gap junctions, respectively. This study was conducted to determine whether Cx43 expression is affected by the mutation of the PKP-2 gene in patients with ARVC. A novel mutation was detected in a typical patient with ARVC. The mutated gene was transfected into rat mesenchymal stem cells expressing Cx43 through a pReversied-M-29 plasmid. Cx43 expression was detected using quantitative polymerase chain reaction analysis. Cx43 expression was significantly decreased in the mutant PKP-2 group compared with that in the wild-type PKP-2 group. In conclusion, PKP-2 affected Cx43 expression at the gene transcription level in the patient with ARVC.
机译:心律失常性右室心肌病(ARVC)是一种桥体疾病。桥粒和间隙连接是心脏嵌入盘的重要结构组成部分。蛋白质plakophilin-2(PKP-2)和connexin43(Cx43)分别是桥粒和间隙连接的组成部分。进行这项研究以确定在ARVC患者中Cx43表达是否受到PKP-2基因突变的影响。在典型的ARVC患者中检测到新的突变。突变的基因通过pReversied-M-29质粒转染到表达Cx43的大鼠间充质干细胞中。使用定量聚合酶链反应分析检测Cx43表达。与野生型PKP-2组相比,突变型PKP-2组的Cx43表达显着降低。总之,PKP-2在ARVC患者的基因转录水平上影响Cx43表达。

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