Chinese Journal of Tissue Engineering Research ›› 2023, Vol. 27 ›› Issue (1): 66-71.doi: 10.12307/2022.984

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miR-31 promotes the proliferation and migration of bone marrow mesenchymal stem cells

Zhang Yujuan1, Yuan Yitong1, Du Ruochen1, Tian Feng1, Fu Yuan2, Wang Chunfang1   

  1. 1Experimental Animal Center, Shanxi Medical University, Taiyuan 030001, Shanxi Province, China; 2Department of Pharmacology, College of Basic Medical Sciences, Shanxi Medical University, Jinzhong 030619, Shanxi Province, China
  • Received:2021-12-18 Accepted:2022-02-16 Online:2023-01-08 Published:2022-06-02
  • Contact: Wang Chunfang, MD, Professor, Experimental Animal Center, Shanxi Medical University, Taiyuan 030001, Shanxi Province, China
  • About author:Zhang Yujuan, Master candidate, Experimental Animal Center, Shanxi Medical University, Taiyuan 030001, Shanxi Province, China
  • Supported by:
    the National Natural Science Foundation of China, No. 81371384 (to WCF); the National Natural Science Youth Foundation of China, No. 82001326 (to YYT); the Applied Basic Research Program Project of Shanxi Province, No. 201901D211319 (to YYT)

Abstract: BACKGROUND: Bone marrow mesenchymal stem cells have been widely used in the clinical treatment of neurodegenerative-related diseases, but their efficacy is reduced by low cell survival and migration rates at the site of injury. 
OBJECTIVE: To investigate whether miR-31 can enhance the migration and proliferation of bone marrow mesenchymal stem cells. 
METHODS: Bone marrow mesenchymal stem cells from C57BL/6 mice were cultured and identified, and the cells were divided into control, miR-31 agomir, and miR-31 antagomir groups. Bone marrow mesenchymal stem cells at passage 3 were inoculated in six-well plates (1×105/well). When the cells reached 50%-80% fusion, miR-31 agomir and miR-31 antagomir were added to the six-well plates after dilution with serum-free DMEM/F12. After 24 hours of transfection, the proliferation level of cells was analyzed by CCK-8 assay as well as the migration ability of cells was analyzed by Transwell assay. Protein expression of matrix metalloproteinase 2 and CXC chemokine receptor 4 was detected by western blot assay. 
RESULTS AND CONCLUSION: (1) miR-31 was successfully transfected with bone marrow mesenchymal stem cells without transfection reagents and emitted red fluorescence. (2) After transfection, the proliferation ability of cells in the miR-31 agomir group was enhanced compared with the control group, which increased proportionally with time (P < 0.05). Compared with the control group, miR-31 promoted the migratory ability of bone marrow mesenchymal stem cells in the miR-31 agomir group (P < 0.05) and also upregulated protein expression of matrix metalloproteinase 2 and CXC chemokine receptor 4 (P < 0.05). (3) The results indicated that miR-31 could improve the proliferation ability of bone marrow mesenchymal stem cells and promote the migration of bone marrow mesenchymal stem cells, which provides a basic study for efficient targeting of mesenchymal stem cell migration to the site of injury. 

Key words: mesenchymal stem cell, bone marrow mesenchymal stem cell, microRNA, miR-31, cell migration, spinal cord injury, CXC chemokine receptor 4, matrix metalloproteinase 2

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