机构：[1]Cardiovascular Center, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China首都医科大学附属北京同仁医院首都医科大学附属同仁医院[2]Department of Pathology, Beijing Tongren Hospital, Capital Medical University, Beijing, China医技科室病理科首都医科大学附属北京同仁医院首都医科大学附属同仁医院[3]Core Facility for Protein Research, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China[4]National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China[5]Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool, UK[6]Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark[7]Department of Endocrinology, Beijing Key Laboratory of Diabetes Research and Care, Beijing Diabetes Institute, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China临床科室内分泌科研究所糖尿病研究所首都医科大学附属北京同仁医院首都医科大学附属同仁医院[8]Department of Cardiac Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China首都医科大学附属安贞医院[9]Beijing Key Laboratory of Diabetes Research and Care, Beijing Diabetes Institute, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China首都医科大学附属北京同仁医院研究所糖尿病研究所
BackgroundAtrial fibrillation (AF) is associated with increased risk of stroke and mortality. It has been reported that the process of atrial fibrosis was regulated by beta-catenin in rats with AF. However, pathophysiological mechanisms of this process in human with AF remain unclear. This study aims to investigate the possible mechanisms of beta-catenin in participating in the atrial fibrosis using human right atrial appendage (hRAA) tissues .MethodsWe compared the difference of beta-catenin expression in hRAA tissues between the patients with AF and sinus rhythm (SR). The possible function of beta-catenin in the development of AF was also explored in mice and primary cells.ResultsFirstly, the space between the membrane of the gap junctions of cardiomyocytes was wider in the AF group. Secondly, the expression of the gap junction function related proteins, Connexin40 and Connexin43, was decreased, while the expression of beta-catenin and its binding partner E-cadherin was increased in hRAA and cardiomyocytes of the AF group. Thirdly, beta-catenin colocalized with E-cadherin on the plasma membrane of cardiomyocytes in the SR group, while they were dissociated and accumulated intracellularly in the AF group. Furthermore, the expression of glycogen synthase kinase 3 beta (GSK-3 beta) and Adenomatous Polyposis Coli (APC), which participated in the degradation of beta-catenin, was decreased in hRAA tissues and cardiomyocytes of the AF group. Finally, the development of atrial fibrosis and AF were proved to be prevented after inhibiting beta-catenin expression in the AF model mice.ConclusionsBased on human atrial pathological and molecular analyses, our findings provided evidence that beta-catenin was associated with atrial fibrosis and AF progression.
基金：
National Natural Science Foundation of China; Qing Bian from Center for Biological Imaging
第一作者机构：[1]Cardiovascular Center, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China
通讯作者：
推荐引用方式(GB/T 7714)：
Bai Ying,Li Rui,Hao Jun-Feng,et al.Accumulated β-catenin is associated with human atrial fibrosis and atrial fibrillation[J].JOURNAL OF TRANSLATIONAL MEDICINE.2024,22(1):doi:10.1186/s12967-024-05558-0.
APA：
Bai, Ying,Li, Rui,Hao, Jun-Feng,Chen, Lian-Wan,Liu, Si-Tong...&Wang, Hao.(2024).Accumulated β-catenin is associated with human atrial fibrosis and atrial fibrillation.JOURNAL OF TRANSLATIONAL MEDICINE,22,(1)
MLA：
Bai, Ying,et al."Accumulated β-catenin is associated with human atrial fibrosis and atrial fibrillation".JOURNAL OF TRANSLATIONAL MEDICINE 22..1(2024)
医学