Chinese Journal of Tissue Engineering Research ›› 2013, Vol. 17 ›› Issue (1): 92-97.doi: 10.3969/j.issn.2095-4344.2013.01.015

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Effects of drynaria total flavonoid on osteogenic differentiation of rat dental pulp stem cells via PI3K/Akt pathway

Huang Xiao-fei1, Yuan Su-jian1, Yang Cheng2   

  1. 1 Department of Stomatology, General Hospital of the Yangtze River Shipping, Wuhan  430010, Hubei Province, China
    2 Department of Stomatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan  430022, Hubei Province, China
  • Received:2012-03-21 Revised:2012-05-16 Online:2013-01-01 Published:2013-01-01
  • Contact: Yang Cheng, M.D., Professor, Chief physician, Doctoral supervisor, Department of Stomatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China yangc715@126.com
  • About author:Huang Xiao-fei★, Master, Physician, Department of Stomatology, General Hospital of the Yangtze River Shipping, Wuhan 430010, Hubei Province, China huangxf84@yahoo.com.cn

Abstract:

BACKGROUND: PI3K/Akt pathway may play an important regulative role in osteogenic differentiation of dental pulp stem cells induced by drynaria total flavonoid.  
OBJECTIVE: To explore the effects of total flavonoids of drynaria on osteogenic differentiation of rat dental pulp stem cells and investigate the role of PI3K/Akt pathway in the induced differentiation of rat dental pulp stem cells.
METHODS: Rat dental pulp stem cells were harvested by enzymatic digestion, cultured and identified by immunohistochemical staining. The dental pulp stem cells were cultured in media with different concentrations of drynaria total flavonoid (0.01 g/L, 0.05 g/L and 0.1 g/L). Alkaline phosphatase activities and formation of calcified tubercles in cells were determined in each group. Phosphorylated Akt expression in cells was detected by western blot method in each group.
RESULTS AND CONCLUSION: Dental pulp stem cells were positive for CD44 and CD29 expression, but they were negative for CD34. Compared to the blank control group, alkaline phosphatase activities, formation of calcified tubercles and phosphorylated Akt expression were significantly increased in the drynaria total flavonoid group in a dose- and time-dependent manner. These findings suggest that drynaria total flavonoid can promote the osteogenic differentiation of rat dental pulp stem cells, and this effect is likely mediated by PI3K/Akt pathway.

Key words: stem cells, stem cells and traditional Chinese medicine, dental pulp stem cells, drynaria total flavonoid, PI3K/Akt pathway, osteogenic differentiation, stem cell photographs-containing paper

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