Hamostaseologie 2023; 43(04): 271-280
DOI: 10.1055/a-2013-0336
Original Article

Inhibition of MicroRNA-122-5p Relieves Myocardial Ischemia-Reperfusion Injury via SOCS1

Authors

  • Jun Zhang

    1   Department of Cardiology, Chengdu First People's Hospital, Chengdu, Sichuan, People's Republic of China
  • Li Fu

    1   Department of Cardiology, Chengdu First People's Hospital, Chengdu, Sichuan, People's Republic of China
  • Jing Zhang

    1   Department of Cardiology, Chengdu First People's Hospital, Chengdu, Sichuan, People's Republic of China
  • Bo Zhou

    1   Department of Cardiology, Chengdu First People's Hospital, Chengdu, Sichuan, People's Republic of China
  • Yanrong Tang

    1   Department of Cardiology, Chengdu First People's Hospital, Chengdu, Sichuan, People's Republic of China
  • Zhenzhen Zhang

    1   Department of Cardiology, Chengdu First People's Hospital, Chengdu, Sichuan, People's Republic of China
  • Tongqing Gu

    2   School of Foreign Languages, Chengdu University of Information Technology, Chengdu, Sichuan, People's Republic of China

Funding This study was supported by the National Natural Science Foundation of China (no. 81270220).
Preview

Abstract

Objective Evidence has shown that microRNA (miR)-122–5p is a diagnostic biomarker of acute myocardial infarction. Here, we aimed to uncover the functions of miR-122–5p in the pathological process of myocardial ischemia-reperfusion injury (MI/RI).

Methods An MI/RI model was established by left anterior descending coronary artery ligation in mice. The levels of miR-122–5p, suppressor of cytokine signaling-1 (SOCS1), phosphorylation of Janus kinase 2 (p-JAK2), and signal transducers and activators of transcription (p-STAT3) in the myocardial tissues of mice were measured. Downregulated miR-122–5p or upregulated SOCS1 recombinant adenovirus vectors were injected into mice before MI/RI modeling. The cardiac function, inflammatory response, myocardial infarction area, pathological damage, and cardiomyocyte apoptosis in the myocardial tissues of mice were evaluated. Cardiomyocytes were subjected to hypoxia/reoxygenation (H/R) injury and cardiomyocyte biological function was tested upon transfection of miR-122–5p inhibitor. The target relation between miR-122–5p and SOCS1 was evaluated.

Results miR-122–5p expression and p-JAK2 and p-STAT3 expression were high, and SOCS1 expression was low in the myocardial tissues of MI/RI mice. Decreasing miR-122–5p or increasing SOCS1 expression inactivated the JAK2/STAT3 pathway to alleviate MI/RI by improving cardiac function and reducing inflammatory reaction, myocardial infarction area, pathological damage, and cardiomyocyte apoptosis in mice. Silencing of SOCS1 reversed depleted miR-122–5p-induced cardioprotection for MI/RI mice. In vitro experiments revealed that the downregulation of miR-122–5p induced proliferative, migratory, and invasive capabilities of H/R cardiomyocytes while inhibiting apoptosis. Mechanically, SOCS1 was a target gene of miR-122–5p.

Conclusion Our study summarizes that inhibition of miR-122–5p induces SOCS1 expression, thereby relieving MI/RI in mice.

Ethical Statement

Experimental approval was signed by the Ethics Committee of Chengdu First People's Hospital. Animal suffering was minimized as much as possible.


Supplementary Material



Publication History

Received: 26 August 2022

Accepted: 11 January 2023

Article published online:
07 March 2023

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