Differences in atrial fibrillation‑associated proteins between the left and right atrial appendages from patients with rheumatic mitral valve disease: A comparative proteomic analysis

风湿性二尖瓣疾病患者左、右心耳房颤相关蛋白的差异:比较蛋白质组学分析

阅读:11
作者:Hai Liu, Guangxian Chen, Hongsheng Zheng, Han Qin, Mengya Liang, Kangni Feng, Zhongkai Wu

Abstract

The majority of proteomic studies have focused on identifying atrial fibrillation (AF)-associated proteins in the right atrium (RA), thus potential differences in AF‑associated proteins between the RA and left atrium (LA) remain unknown. The aim of the present study was to perform proteomic analysis to compare the potential differences in AF‑associated proteins between the right atrial appendage (RAA) and left atrial appendage (LAA) in patients with rheumatic mitral valve disease (RMVD). RAA and LAA tissues were obtained from 18 patients with RMVD (10 with AF) during mitral valve replacement surgery. Two‑dimensional fluorescence difference gel electrophoresis (2‑D DIGE) proteomics analysis was performed using these tissues to identify AF‑associated proteins in RAA and LAA. Subsequently, the proteomics data was validated using western blot analysis of nine selected proteins. In RAA, 32 AF‑associated proteins were significantly dysregulated (15 upregulated and 17 downregulated). In LAA, 31 AF‑associated proteins were significantly dysregulated (13 upregulated and 18 downregulated). Among these AF‑associated proteins, 17 were AF‑associated in both RAA and LAA, 15 were AF‑associated only in RAA, and 14 were AF‑associated only in LAA. Amongst the differentially expressed proteins, western blot analysis validated the results for 6 AF‑associated proteins, and demonstrated similar distributions in RAA and LAA compared with the 2‑D DIGE results. Of these proteins, 2 proteins were AF‑associated in both RAA and LAA, 2 were AF‑associated only in RAA, and 2 were AF‑associated only in LAA. Additionally, the different distributions of AF‑associated proteins in the RAA and LAA of patients with RMVD was analyzed, which may reflect the different regulatory mechanisms of the RA and LA in AF. These findings may provide new insights into the underlying molecular mechanisms of AF in patients with RMVD.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。