中国临床解剖学杂志 ›› 2012, Vol. 30 ›› Issue (1): 84-86.

• 实验研究 • 上一篇    下一篇

离子硅对成骨细胞NF-kappa B核内转录因子活性的影响

邱小忠1, 王永魁1, 王乐禹1, 余 磊1, 王国保2   

  1. 1.南方医科大学人体解剖学教研室  广东省组织构建与检测重点实验室,  广州   510515;
    2.南方医科大学南方医院肾内科,  广州   510515
  • 收稿日期:2011-10-30 出版日期:2012-01-25 发布日期:2012-02-03
  • 通讯作者: 王国保,副主任医师,副教授,E-mail: wgbandyl@fimmu.com E-mail:qqiuxzh@yahoo.com.cn
  • 作者简介:共同第一作者:邱小忠(1968-),男,医学博士,副教授,研究方向:组织工程E - mail: qqiuxzh@yahoo. com. cn 王永魁(1985-),男,在读硕士,研究方向:组织工程E- mail:wyk8520586@126.com
  • 基金资助:

    广州市科技计划项目(11C32120736)

Effects of silicon on the activity of the nuclear transcription factor NF-kappa B in osteoblasts

QIU Xiao-zhong1,WANG Yong-kui1,WANG Le-yu1,YU Lei1, WANG Guo-bao2   

  1. 1.Department of Anatomy, Southern Medical University,Guangzhou 510515,China; 2. Department of Nephrology, Nanfang Hospital Affiliated to Southern Medical University, Guangzhou 510515, China
  • Received:2011-10-30 Online:2012-01-25 Published:2012-02-03

摘要:

目的 研究离子硅对体外培养的成骨细胞NF-kappa B核转录因子活性的影响。  方法 分别用终浓度为1 mmol/L和2 mmol/L离子硅(SiO32-)处理MC3T3-E1成骨细胞,处理时间分别为6、12、24和48 h,设置对照组(不加处理因素);采用流式细胞术检测细胞周期,计算细胞的增殖指数;Western blotting方法检测NF-kappa B信号通路的相关蛋白表达量及其变化。  结果 流式细胞术结果显示,与对照组相比,1 mmol/L浓度的离子硅处理24 h组和48 h组,MC3T3-E1细胞增殖明显;Western blot结果显示,1 mmol/L浓度的离子硅促进成骨细胞增殖与p-NF-kappa B表达上升密切相关。  结论 骨材料中释放的微量的硅不会引起成骨细胞损伤,相反,微量的硅酸盐可能通过激活NF-kappa B诱导成骨细胞增殖。

关键词: 硅, 生物材料, 骨修复, 成骨细胞, NF-kappa B

Abstract:

Objective To explore the effects of silicon on the activity of nuclear transcription factor NF-kappa B in osteoblasts cultured in vitro. Methods MC3T3-E1 osteoablasts were processed by sodium silicate solution (SiO32-) with the final concentration of 1mM and 2 mM for 6h, 12h, 24h and 48h, respectively. Untreated cells were taken as the control groups. Flow cytometry was used to detect the cell cycle and calculate cell proliferation index. Western blotting was used to detect the expressions and changes of NF-kappa B signaling pathway related proteins. Results Compared with the controls, significant proliferation of MC3T3-E1 cells was found in the 24h and 48h groups treated with 1 mM silicon. Western blot analysis showed that the pro-proliferation effect of 1 mM silicon on osteoblasts was closely related to the high-expression of p-NF-kappa B. Conclusions Trace amounts of silicon released from bone materials can not cause damage of osteoblasts, on contrary, trace amounts of silicate may induce proliferation of osteoblasts by activating NF-kappa B signaling pathway.

Key words: Silicon;   , Biomaterial; Bone repair; Osteoblast; NF-kappa B

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