KMID : 0381120190410121467
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Genes and Genomics 2019 Volume.41 No. 12 p.1467 ~ p.1474
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Up-regulation of miR-27 extenuates lipopolysaccharide-induced injury in H9c2 cells via modulating ICAM1 expression
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Xiang Jing-Fang
Yu Jian-Chun Zhu Jian-You
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Abstract
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Background: MiR-27 has been found to present an overt myocardial expression during cardiogenesis. However, whether miR-27 involves in myocarditis development and the possible molecular mechanism remain unknown. The purpose of this study was to investigate the biological characteristic of miR-27 in LPS-damaged H9c2 cells.
Methods: H9c2 cells were treated with lipopolysaccharide (LPS, 10 ¥ìg/ml) for 12 h to form cell injury. MiR-27 mimic and inhibitor were used to up-regulate or down-regulate miR-27 expression. MTT assay and flow cytometry analysis were conducted to test cell viability and apoptosis. The relative RNA expression level of miR-27 and intercellular adhesion molecule 1 (ICAM1) was determined by qRT-PCR. Luciferase reporter gene assay was utilized to confirm the interaction between miR-27 and ICAM1. Western blot was used to determine the protein expression levels.
Results: We observed that LPS treatment significantly decreased the level of miR-27 in H9c2 cells. Moreover, LPS exposure suppressed cell viability, promoted cell apoptosis and increased the relative expression of p-NF-¥êB p65/NF-¥êB p65 and p-I¥êB¥á/I¥êB¥á. Up-regulation of miR-27 increased cell proliferation and reduced cell apoptosis, while down-regulation of miR-27 suppressed cell growth and promoted cell apoptosis. ICAM1 was predicted and verified as a target of miR-27, and the expression of ICAM1 is negatively regulated by miR-27. The relative expression of p-NF-¥êB p65/NF-¥êB p65 and p-I¥êB¥á/I¥êB¥á was dramatically decreased by miR-27 mimic and increased by miR-27 inhibitor.
Conclusion: Our study illustrated that up-regulation of miR-27 exhibits a protective effect on LPS-damaged H9c2 cells, which may be achieved by regulating ICAM1 and NF-¥êB signaling.
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KEYWORD
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Myocarditis, miR-27, NF-¥êB signaling pathway, ICAM1, Luciferase reporter gene assay
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