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DOI 10.1159/000453187

Медицинская библиотека · Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2016

MiR-22 may Suppress Fibrogenesis by Targeting TGFβR I in Cardiac Fibroblasts.

Hong Yuan, Cao Huaming, Wang Qiang, Ye Jianlin, Sui Lijun, Feng Jinhua, Cai Xiaojun, Song Huizhu, Zhang Xiuhong, Chen Xichuang

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Аннотация

BACKGROUND/AIMS: Cardiac fibrosis after myocardial infarction (MI) has been identified as a key factor in the development of heart failure, but the mechanisms undelying cardiac fibrosis remained unknown. microRNAs (miRNAs) are novel mechanisms leading to fibrotic diseases, including cardiac fibrosis. Previous studies revealed that miR-22 might be a potential target. However, the roles and mechanisms of miR-22 in cardiac fibrosis remained ill defined. The present study thus addressed the impact of miR-22 in cardiac fibrosis.

METHODS

After seven days following coronary artery occlusion in mice, tissues used for histology were collected and processed for Masson's Trichrome staining. In addition, cardiac fibroblasts were transfected with mimics and inhibitors of miR-22 using Lipofectamin 2000, and luciferase activity was measured in cell lysates using a luciferase assay kit. Western blotting was used to detect the expression of collagen1, α-SMA and TGFβRI proteins levels, and real time-PCR was employed to measure the Col1α1, Col3α1, miR-22 and TGFβRI mRNA levels.

RESULTS

In this study, we found that miR-22 was dynamically downregulated following MI induced by permanent ligation of the left anterior descending coronary artery for 7 days, an effect paralleled by significant collagen deposition. Inhibition of miR-22 with AMO-22 resulted in increased expression of Col1α1, Col3α1 and fibrogenesis in cultured cardiac fibroblasts. Conversely, overexpression of miR-22 in cultured cardiac fibroblasts significantly abrogated angiotensin II-induced collagen formation and fibrogenesis. Furthermore, we found that TGFβRI is a direct target for miR-22, and downregulation of TGFβR may have mediated the antifibrotic effect of miR-22.

CONCLUSION

Our data clearly demonstrate that miR-22 acts as a novel negative regulator of angiotensin II-induced cardiac fibrosis by suppressing the expression of TGFβRI in the heart and may represent a new potential therapeutic target for treating cardiac fibrosis.

Для цитирования: Hong Yuan, Cao Huaming, Wang Qiang, Ye Jianlin, Sui Lijun, Feng Jinhua, Cai Xiaojun, Song Huizhu, Zhang Xiuhong, Chen Xichuang. MiR-22 may Suppress Fibrogenesis by Targeting TGFβR I in Cardiac Fibroblasts.. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology. 2016. DOI: 10.1159/000453187.

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