基础医学与临床 ›› 2011, Vol. 31 ›› Issue (6): 647-651.

• 研究论文 • 上一篇    下一篇

NR2F2促进小鼠MC3T3-E1前成骨细胞增殖

王崧,熊霞辉,朱宁,陈梅红   

  1. 中国医学科学院基础医学研究所
  • 收稿日期:2011-03-09 修回日期:2011-04-12 出版日期:2011-06-05 发布日期:2011-06-06
  • 通讯作者: 陈梅红 E-mail:chenmhxc@gmail.com
  • 基金资助:
    国家重点基础研究发展计划

NR2F2 accelerates mouse MC3T3-E1 pre-osteoblast proliferation

Song WANG1,Xia-hui XIONG2,Ning ZHU2,Mei-Hong CHEN1   

  1. 1. Institute of Basic Medical Sciences, CAMS&PUMC
    2.
  • Received:2011-03-09 Revised:2011-04-12 Online:2011-06-05 Published:2011-06-06
  • Contact: Mei-Hong CHEN E-mail:chenmhxc@gmail.com

摘要: 目的 探讨NR2F2基因对小鼠前成骨细胞增殖的影响。方法 用实时定量PCR检测mRNA表达量,MTS法检测细胞增殖,流式细胞术检测细胞周期,ELISA-Brdu法检测细胞DNA合成速度。结果 在小鼠MC3T3-E1前成骨细胞增殖速度加快时,NR2F2基因的表达增高至对照的4.57±0.30倍(p<0.01)。过表达NR2F2基因促使MC3T3-E1细胞增殖速度加快,细胞数量增加(p<0.01),细胞周期中S期细胞比例明显升高,为对照组的2倍,G2/M期比例也有增加(p<0.05)。过表达NR2F2基因使MC3T3-E1细胞的Brdu掺入率增高,DNA的合成加速(p<0.01)。结论NR2F2使S期细胞比例增加,促进小鼠前成骨细胞MC3T3-E1的增殖速度。

关键词: Nr2f2, MC3T3-E1细胞, 细胞增殖

Abstract: Objective To study the role of NR2F2 in murine pre-osteoblast proliferation. Methods Quantitative real-time PCR was used to measure the mRNA level, MTS assay was used to assess the cell proliferation rate, flow cytometry was used to figure out the cell cycle distribution, and ELISA-Brdu was used to check the rate of DNA synthesis. Results When murine pre-osteoblast MC3T3-E1 cell proliferation was accelerated, the expression level of NR2F2 remarkably increased to 4.57±0.30 (p<0.01) fold compared with that of the control. Over-expression of NR2F2 accelerated MC3T3-E1 cell proliferation (p<0.01), and the proportion of cells in S phase markedly increased to 2 fold compared with that of the control, and the proportion of cells in G2/M phase also went up (p<0.05). More Brdu was incorporated into NR2F2 over-expressing cells, indicating the increase of DNA replication rate (p<0.01). Conclusion NR2F2 accelerates murine pre-osteoblast MC3T3-E1 proliferation through increasing the proportion of cells in S phase.

Key words: Nr2f2, MC3T3-E1 cell, cell proliferation

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