Literature DB >> 25809568

Cardioprotective Effect of MicroRNA-21 in Murine Myocardial Infarction.

Guo-Long Gu1, Xiao-Lin Xu2, Xiao-Tian Sun2,3, Ji Zhang4, Chang-Fa Guo3, Chun-Sheng Wang3, Bing Sun5, Gong-Liang Guo5, Ke Ma5, Yuan-Yuan Huang5, Li-Qun Sun5, Yi-Qing Wang2.   

Abstract

INTRODUCTION: To investigate the cardioprotective effect of MicroRNA-21 (miR-21) in murine myocardial infarction (MI).
METHODS: Forty C57BL/6 male mice were divided into sham group, MI group, LV-GFP group, and miR-21 group. Mice in the MI group, LV-GFP group, and miR-21 group were subjected to MI by left anterior descending artery (LAD) ligation, while chest was opened/closed without ligation in sham group. In MI group, expression of miR-21 in the MI area and its surrounding areas was detected at 1st, 2nd, and 4th week after experiment. Subsequently, lentivirus expressing miR-21 and lentivirus that did not express miR-21 were transfected into mice left ventricular cavity of miR-21 group and LV-GFP group, respectively. Cardiac function, MI size, miR-21 expression, collagen I level, fibronectin content, number of α-SMA-positive cells, number of apoptotic cells, apoptosis-related factors were compared between the three groups.
RESULTS: Compared with sham group, miR-21 levels in MI group were significantly decreased in the 1st week and 2nd week, but were almost the same in the 4th week. Left ventricular fractional shortening (LVFS) and left ventricular ejection fraction (LVEF) in the miR-21 group improved compared to the LV-GFP group. In miR-21 group, myocardial infarct size reduced by 36.9% in comparison with LV-GFP group. Compared to sham group, miR-21 expression in the miR-21 group and LV-GFP group decreased significantly. In the miR-21 group, collagen I level, fibronectin content and number of α-SMA-positive cells of miR-21 decreased significantly compared to the LV-GFP group. The number of apoptotic cells in the MI areas of the miR-21 group was significantly less than the LV-GFP group. Compared with the LV-GFP group, Bcl-2 level and the ratio of Bcl-2 to Bax were significantly increased, and the levels of Bax and Caspase-3 decreased.
CONCLUSIONS: Our results suggest miR-21 is an important regulatory molecule in the pathophysiology of MI.
© 2015 John Wiley & Sons Ltd.

Entities:  

Keywords:  Cardiac function; Cardioprotective effect; Cell apoptosis; MicroRNA-21; Myocardial infarction; Transfection

Mesh:

Substances:

Year:  2015        PMID: 25809568     DOI: 10.1111/1755-5922.12118

Source DB:  PubMed          Journal:  Cardiovasc Ther        ISSN: 1755-5914            Impact factor:   3.023


  20 in total

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6.  Serum-Derived Extracellular Vesicles Protect Against Acute Myocardial Infarction by Regulating miR-21/PDCD4 Signaling Pathway.

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8.  The microRNA miR-21 conditions the brain to protect against ischemic and traumatic injuries.

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Journal:  Cond Med       Date:  2017-12-15

9.  MicroRNA-199a acts as a potential suppressor of cardiomyocyte autophagy through targeting Hspa5.

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10.  A novel system-level approach using RNA-sequencing data identifies miR-30-5p and miR-142a-5p as key regulators of apoptosis in myocardial infarction.

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