Chinese Journal of Tissue Engineering Research ›› 2010, Vol. 14 ›› Issue (24): 4390-4392.doi: 10.3969/j.issn.1673-8225.2010.24.005

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Effect of estrogen on vascular endothelial growth factor expression in rat osteoblasts

Pan Jin-ping, Yin Yun-sheng, Li Peng-biao, Wen Wei-jing   

  1. Department of Orthopaedics, Second Clinical Hospital, Shanxi Medical University, Taiyuan   030001, Shanxi Province, China
  • Online:2010-06-11 Published:2010-06-11
  • Contact: Yin Yun-sheng, Chief physician, Master’s supervisor, Department of Orthopaedics, Second Clinical Hospital, Shanxi Medical University, Taiyuan 030001, Shanxi Province, China yunshengyin@hotmail.com
  • About author:Pan Jin-ping★, Studying for master’s degree, Department of Orthopaedics, Second Clinical Hospital, Shanxi Medical University, Taiyuan 030001, Shanxi Province, China ibmapple33@163.com

Abstract:

BACKGROUND: Vascular endothelial growth factor (VEGF) is a major angiogenesis factor, characterizing by promoting cell division, proliferation, cytoplasm calcification and aggregation, as well as inducing angiogenesis; on the other hand, it also adjusts proliferation, differentiation, and functional activity of osteoblast and osteoclast.
OBJECTIVE: To investigate the effect of estrogen on VEGF expression in rat osteoblasts.
METHODS: Calvaria osteoblasts derived from 48-hour-old rats were cultured to obtain osteoblast. RT-PCR was employed to detect the VEGF mRNA expression following induction of 17β-estradiol at concentrations of 10-10, 10-8, 10-6, and 10-4 mol/L.
RESULTS AND CONCLUSION: RT-PCR demonstrated that VEGF mRNA was stably expressed in primary cultured osteoblast. Semi-quantitative analysis demonstrated that VEGF mRNA expression was in a certain law following 17β-estradiol induction at varying concentrations, i.e., with the increasing concentration of 17β-estradiol, VEGF mRNA expression was increased. At 10-6 mol/L, the VEGF mRNA expression peaked, and when 17β-estradiol was over this dose, the expression was gradually decreased. This suggested that estrogen promoted VEGF mRNA expression, showing a dose-dependent manner.

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