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[Screening of the Optimum Medium for Rat Mesenchymal Stem Cells].
Wang, Jing-Ge; Yu, Xiao-Qin; Wen, Ji-Rui; Zhu, Guang-Guang; Bao, Ming-Yue; He, Xue-Ling; Li, Liang.
Affiliation
  • Wang JG; Institute of Biomedical Engineering, West China School of Basic Medical Science & Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Yu XQ; Institute of Biomedical Engineering, West China School of Basic Medical Science & Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Wen JR; Institute of Biomedical Engineering, West China School of Basic Medical Science & Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Zhu GG; Institute of Biomedical Engineering, West China School of Basic Medical Science & Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Bao MY; Institute of Biomedical Engineering, West China School of Basic Medical Science & Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • He XL; Institute of Biomedical Engineering, West China School of Basic Medical Science & Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Li L; Institute of Biomedical Engineering, West China School of Basic Medical Science & Forensic Medicine, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban ; 50(6): 891-895, 2019 Dec.
Article in Zh | MEDLINE | ID: mdl-31880123
ABSTRACT

OBJECTIVE:

To investigate the effect of three different cell culture mediums, DMEM-LG, α-MEM and DMEM/F12, on the growth of rat bone marrow mesenchymal stem cells (BMSCs) in vitro, and so that to screen out the most suitable medium for in vitro culturing the rat BMSCs.

METHODS:

BMSCS were isolated from the femur and tibia of SD rats by whole bone marrow differential adherence method. The isolated cells were then cultured with three culture mediums, DMEM-LG, α-MEM and DMEM/F12. The rat BMSCs morphology, adhesion, proliferation, the time of passage and the number the colony at day 14 in three mediums respectively were observed with inverted phase contrast microscopy and compared. Flow cytometry was used to identify and observe the effects of different mediums on the surface antigen expression of rats BMSCs.

RESULTS:

Compared with the other two groups of media, BMSCs cultured in DMEM-LG had shorter colony formation time, shorter first passage time, more clone formation (14±2) and showed uniform morphology and the highest attachment efficiency (47.0±2.8)%. Meanwhile, BMSCs cultured with DMEM-LG entered logarithmic growth phase after only 4 days of culturing and showed the highest average specific growth rate and the largest average number of propagations per unit time. The total number of cells reached about (2.2-2.7)×105 mL-1 within three days. The cells cultured with 3 mediums were all identified as rat BMSCs, and the expression of surface antigen in BMSCs was not significantly affected by different media.

CONCLUSION:

DMEM-LG is more suitable for proliferation of rat BMSCs in vitro.
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Collection: 01-internacional Database: MEDLINE Main subject: Mesenchymal Stem Cells Type of study: Diagnostic_studies / Screening_studies Limits: Animals Language: Zh Journal: Sichuan Da Xue Xue Bao Yi Xue Ban Year: 2019 Type: Article Affiliation country: China
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Mesenchymal Stem Cells Type of study: Diagnostic_studies / Screening_studies Limits: Animals Language: Zh Journal: Sichuan Da Xue Xue Bao Yi Xue Ban Year: 2019 Type: Article Affiliation country: China