Proliferation in vitro of bone marrow-derived mesenchymal stem cells in different culture meeia in rabbits.
Linwei Xin, Lingyun Wei, Qiang Li, Jicun Tang
Abstract
Linwei Xin, Lingyun Wei, Qiang Li, Jicun Tang
Abstract
Objective To investigate the effects of different culture media on the proliferation in vitro of bone marrow-derived mesenchymal stem cells.Methods Bone marrow was Abstracted from the intertrochanter of the femur of 2-month New Zealand rabbits and purification of mesenchymal stem cells was determined by a density gradient centrifugation method.The cells were cultured in 4 kinds of culture media:DMEM-high glucose(10%FBS),DMEM-low glucose(10%FBS),DMEM-low glucose(15%FBS)and DMEM-low glucose(20%FBS).Cells of passage one were detected the expansion multiple and cells of passage two measured the growth and mineralization of cells.Results The expansion multiple was 16.20±1.60 and the colony-forming number(CFN)was 6.11±1.17 in the DMEM-low glucose(15%FBS)group,which were significantly higher than those in the other three groups.Conclusion DMEM-low glucose(15%FBS)is more suitable for cultivation of MSCs than the other three media.
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Objective To investigate the effects of different culture media on the proliferation in vitro of bone marrow-derived mesenchymal stem cells.Methods Bone marrow was Abstracted from the intertrochanter of the femur of 2-month New Zealand rabbits and purification of mesenchymal stem cells was determined by a density gradient centrifugation method.The cells were cultured in 4 kinds of culture media:DMEM-high glucose(10%FBS),DMEM-low glucose(10%FBS),DMEM-low glucose(15%FBS)and DMEM-low glucose(20%FBS).Cells of passage one were detected the expansion multiple and cells of passage two measured the growth and mineralization of cells.Results The expansion multiple was 16.20±1.60 and the colony-forming number(CFN)was 6.11±1.17 in the DMEM-low glucose(15%FBS)group,which were significantly higher than those in the other three groups.Conclusion DMEM-low glucose(15%FBS)is more suitable for cultivation of MSCs than the other three media.
Key concepts: Mesenchymal stem cell, In vitro, Bone marrow, Stem cell, Andrology, Centrifugation, Differential centrifugation, Cell culture