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      https://www.ias.ac.in/article/fulltext/jbsc/046/0113

    • Keywords

       

      17 β -Estradiol; miR-320/RUNX2 axis; osteoporosis; oxidative stress

    • Abstract

       

      The aim of this study is to investigate the effect and mechanism of 17 beta-estradiol (E2) on oxidative stress in theosteoblasts. An oxidative stress-induced damage model was established using H2O2 in MC3T3-E1 cells, andH2O2-induced cells were treated with E2. The results indicated that E2 attenuated oxidative stress in H2O2-induced MC3T3-E1 cells. In addition, H2O2 upregulated the expression of miR-320-3p and downregulated thatof RUNX2, but these changes were counteracted by E2. Thereafter, we verified the interactive relationshipbetween miR-320-3p and RUNX2. Then, H2O2-induced MC3T3-E1 cells were transfected with miR-320-3pmimics or inhibitors and treated with E2. The results indicated that miR-320-3p inhibition suppressed H2O2-induced inflammation, apoptosis, and oxidative stress and promoted the osteogenic differentiation of MC3T3-E1 cells by regulating RUNX2, ALP, and OCN, and this effect was further strengthened by E2. In conclusion,the findings suggest that E2 alleviates oxidative damage in osteoblasts by regulating the miR-320/RUNX2signaling.

    • Author Affiliations

       

      YANYAN XU1 HAO XU1 XIUPING YIN1 XIANLI LIU1 ZHONGXI MA1 ZHIGANG ZHAO1

      1. Department of Orthopaedics, Wuhan Fourth Hospital, Puai Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430033, China
    • Dates

       
  • Journal of Biosciences | News

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