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Role of MicroRNA-34a in Anti-Apoptotic Effects of Granulocyte-Colony Stimulating Factor in Diabetic Cardiomyopathy

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Specialty Endocrinology
Date 2019 Jun 26
PMID 31237127
Citations 10
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Abstract

Background: Recent studies have shown that microRNAs (miRNAs) are involved in the process of cardiomyocyte apoptosis. We have previously reported that granulocyte-colony stimulating factor (G-CSF) ameliorated diastolic dysfunction and attenuated cardiomyocyte apoptosis in a rat model of diabetic cardiomyopathy. In this study, we hypothesized a regulatory role of cardiac miRNAs in the mechanism of the anti-apoptotic effect of G-CSF in a diabetic cardiomyopathy rat model.

Methods: Rats were given a high-fat diet and low-dose streptozotocin injection and then randomly allocated to receive treatment with either G-CSF or saline. H9c2 rat cardiomyocytes were cultured under a high glucose (HG) condition to induce diabetic cardiomyopathy . We examined the extent of apoptosis, miRNA expression, and miRNA target genes in the myocardium and H9c2 cells.

Results: G-CSF treatment significantly decreased apoptosis and reduced miR-34a expression in diabetic myocardium and H9c2 cells under the HG condition. G-CSF treatment also significantly increased B-cell lymphoma 2 (Bcl-2) protein expression as a target for miR-34a. In addition, transfection with an miR-34a mimic significantly increased apoptosis and decreased Bcl-2 luciferase activity in H9c2 cells.

Conclusion: Our results indicate that G-CSF might have an anti-apoptotic effect through down-regulation of miR-34a in a diabetic cardiomyopathy rat model.

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References
1.
Liu L, Zhang G, Liang Z, Liu X, Li T, Fan J . MicroRNA-15b enhances hypoxia/reoxygenation-induced apoptosis of cardiomyocytes via a mitochondrial apoptotic pathway. Apoptosis. 2013; 19(1):19-29. DOI: 10.1007/s10495-013-0899-2. View

2.
Pinti M, Hathaway Q, Hollander J . Role of microRNA in metabolic shift during heart failure. Am J Physiol Heart Circ Physiol. 2016; 312(1):H33-H45. PMC: 5283914. DOI: 10.1152/ajpheart.00341.2016. View

3.
Liu X, Liu S . Role of microRNAs in the pathogenesis of diabetic cardiomyopathy. Biomed Rep. 2017; 6(2):140-145. PMC: 5351040. DOI: 10.3892/br.2017.841. View

4.
Shin J, Lim Y, Song Y, So B, Park J, Fang C . Granulocyte-colony stimulating factor reduces cardiomyocyte apoptosis and ameliorates diastolic dysfunction in Otsuka Long-Evans Tokushima Fatty rats. Cardiovasc Drugs Ther. 2014; 28(3):211-20. DOI: 10.1007/s10557-014-6519-8. View

5.
Cai L, Li W, Wang G, Guo L, Jiang Y, Kang Y . Hyperglycemia-induced apoptosis in mouse myocardium: mitochondrial cytochrome C-mediated caspase-3 activation pathway. Diabetes. 2002; 51(6):1938-48. DOI: 10.2337/diabetes.51.6.1938. View