Atrial overexpression of microRNA-27b attenuates angiotensin II-induced atrial fibrosis and fibrillation by targeting ALK5

• Published in: Human cell : official journal of Human Cell Research Society 2018-07, Vol.31 (3), p.251-260
• Main Authors: Wang, Yanshan, Cai, Heng, Li, Hongmei, Gao, Zhisheng, Song, Kunqing
• Format: Article
• Language: English
• Subjects: Actin; Angiotensin; Angiotensin II; Angiotensin II - pharmacology; Animals; Atrial Fibrillation - chemically induced; Atrial Fibrillation - genetics; Atrial Fibrillation - metabolism; Atrial Fibrillation - therapy; Atrium; Biomedical and Life Sciences; Cell Biology; Collagen (type I); Collagen (type III); Collagen - metabolism; Conduction; Fibrillation; Fibrosis; Gene Expression - genetics; Gynecology; Heart Atria - metabolism; Heart Atria - pathology; Heart diseases; Life Sciences; Male; Mice, Inbred C57BL; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; miRNA; Molecular Targeted Therapy; mRNA; Oncology; Phosphorylation; Phosphorylation - genetics; Plasminogen Activator Inhibitor 1 - metabolism; Plasminogen activator inhibitors; Protein-Serine-Threonine Kinases - genetics; Protein-Serine-Threonine Kinases - metabolism; Receptors, Transforming Growth Factor beta - genetics; Receptors, Transforming Growth Factor beta - metabolism; Reproductive Medicine; Research Article; Signal Transduction - genetics; Smad protein; Smad2 Protein - metabolism; Smooth muscle; Stem Cells; Surgery; Therapeutic applications; Transforming growth factor-b1
• ISSN: 1749-0774; 0914-7470; 1749-0774
• DOI: 10.1007/s13577-018-0208-z

Atrial fibrosis influences atrial fibrillation (AF) development by transforming growth factor beta 1 (TGF-β1)/Smad pathway. Although microRNAs are implicated in the pathogenesis of various diseases, information regarding the functional role of microRNAs in atrial dysfunction is limited. In the present study, we found that microRNA-27b (miR-27b) was the dominant member of miR-27 family expressed in left atrium. Moreover, the expression of miR-27b was significantly reduced after angiotensin II (AngII) infusion. Masson’s trichrome staining revealed that delivery of miR-27b adeno-associated virus to left atrium led to a decrease in atrial fibrosis induced by AngII. The increased expression of collagen I, collagen III, plasminogen activator inhibitor type 1 and alpha smooth muscle actin was also inhibited after miR-27b upregulation. In isolated perfused hearts, miR-27b restoration markedly attenuated AngII-induced increase in interatrial conduction time, AF incidence and AF duration. Furthermore, our data evidence that miR-27b is a novel miRNA that targets ALK5, a receptor of TGF-β1, through binding to the 3′ untranslated region of ALK5 mRNA. Ectopic miR-27b suppressed luciferase activity and expression of ALK5, whereas inhibition of miR-27b increased ALK5 luciferase activity and expression. Additionally, miR-27b inhibited AngII-induced Smad-2/3 phosphorylation without altering Smad-1 activity. Taken together, our study demonstrates that miR-27b ameliorates atrial fibrosis and AF through inactivation of Smad-2/3 pathway by targeting ALK5, suggesting miR-27b may play an anti-fibrotic role in left atrium and function as a novel therapeutic target for the treatment of cardiac dysfunction.