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Chinese Journal of Stomatological Research(Electronic Edition) ›› 2012, Vol. 6 ›› Issue (05): 405-409. doi: 10.3877/cma.j.issn.1674-1366.2012.05.003

• Original Articles • Previous Articles    

The expression of pluripotency markers in the subpopulations of human bone marrow stromal cells

Lu LIU1, Xi WEI1, Jun-qi LING1,(), Zheng-jun PENG1, Li-ping WU1   

  1. 1.Guanghua School of Stomatology,Hospital of Stomatology, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Stomatology,Guangzhou 510055, China
  • Received:2012-05-21 Online:2012-10-01 Published:2025-02-20
  • Contact: Jun-qi LING

Abstract:

Objective

The purpose of this study was to investigate theexpression of pluripotency markers Sox2, c-Myc and hTert in the subpopulations of human bone marrow stromal cells with in vitro culture.

Methods

Human BMSCs were culture with limiting dilution method, 3 samples were selected from fast-, slow-growing clones and mixed culture BMSCs respectively. The expression of Sox2, c-Myc and hTert was investigated by immunofluorescent staining and quantitative Realtime PCR analysis. Statistics analysis was applied.

Results

Sox2 showed positive nucleus expression in fastgrowing clones, and cytoplasm expression in other groups. Sox2 mRNA displayed significantly higher expression level compared with other groups (P<0.05). c-Myc and hTert showed similar expression pattern which demonstrated a nucleus location in fast-growing clones and mixed cultured BMSCs,albeit cytoplasm staining in slow-growing clones. Whereas the c-Myc and hTert mRNA showed no difference among three groups (P>0.05).

Conclusions

BMSCs from fast-growing clones demonstrated higher expression of reprogramming markers compared with slow-growing clones, indicating that colony forming efficiency may be related with the pluripotency and reprogramming capability of BMSCs. c-Myc and hTert may interact cooperatively during this process.

Key words: Bone marrow stromal cells, Subpopulations, Pluripotency markers

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