• 1. Tuberculosis Department, Wuhan Medical Treatment Center, Wuhan 430023, P.R.China;
  • 2. Institute of Biology and Medicine, Wuhan University of Science and Technology, Wuhan 430065, P.R.China;
  • 3. Cardio-Thoracic Surgery Department, Wuhan Puren Hospital, Wuhan 430081, P.R.China;
TAO Lixuan, Email: 309464516@qq.com
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With the oxidative damage model established in rat myocardial cells by hydrogen peroxide (H2O2), the expression of myocardin and nuclear factor erythroid 2-related factor 2 (Nrf2) during oxidative damage and effect of myocardin on Nrf2 were preliminarily explored. The expression of the target gene was increased or decreased by transfection of plasmid DNA or shRNA, respectively. Cell proliferation was detected by sulforhodamine B (SRB) assay. The expression of myocardin mRNA and Nrf2 mRNA was detected by Real-time PCR, and their protein levels were detected by Western blot. The results showed that oxidative damage was induced by H2O2 with an optimized incubation condition of 200 μmol/L H2O2 for 24 hours. H2O2 inhibited expression of myocardin in mRNA and protein levels, and increased expression of Nrf2 in mRNA and protein levels. The overexpression of myocardin or the knockdown of Nrf2 significantly decreased cell viability compared with the control group, while the knockdown of myocardin or the overexpression of Nrf2 significantly increased cell viability. The overexpression of myocardin significantly down-regulated the expression of Nrf2 in mRNA and protein levels, while the knockdown of myocardin dramatically up-regulated the expression of Nrf2. Thus, it is deduced that myocardin may inhibit cell proliferation and Nrf2 may promote cell proliferation. Oxidative damage induced by H2O2 in rat myocardial cell might activate Nrf2-related signaling pathway through down-regulation of myocardin.

Citation: NIE Qi, TAO Lixuan, YU Chengxi, DAI Yuhuan, XIA Ying, LIU Yuting, XIA Zhidan, LI Jiapeng, DONG Jian. Effect of oxidative damage on expression of myocardin and NF-E2-related factor 2 in myocardial cells. Journal of Biomedical Engineering, 2017, 34(4): 585-590. doi: 10.7507/1001-5515.201603009 Copy

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