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静磁场不同处理时间对体外培养成骨细胞增殖与分化的影响
Hits: 2125   Download times: 1179   Received:March 25, 2012    
作者Author单位UnitE-Mail
王嘉琪 WANG Jia-qi 兰州军区兰州总医院骨科研究所,甘肃 兰州 730050 Institute of Orthopaedics,Lanzhou General Hospital of PLA,Lanzhou 730050,Gansu,China  
葛宝丰 GE Bao-feng 兰州军区兰州总医院骨科研究所,甘肃 兰州 730050 Institute of Orthopaedics,Lanzhou General Hospital of PLA,Lanzhou 730050,Gansu,China  
马晓妮 MA Xiao-ni 兰州军区兰州总医院骨科研究所,甘肃 兰州 730050 Institute of Orthopaedics,Lanzhou General Hospital of PLA,Lanzhou 730050,Gansu,China  
周建 ZHOU Jian 兰州军区兰州总医院骨科研究所,甘肃 兰州 730050 Institute of Orthopaedics,Lanzhou General Hospital of PLA,Lanzhou 730050,Gansu,China  
郭晓宇 GUO Xiao-yu 兰州军区兰州总医院骨科研究所,甘肃 兰州 730050 Institute of Orthopaedics,Lanzhou General Hospital of PLA,Lanzhou 730050,Gansu,China  
陈克明 CHEN Ke-ming 兰州军区兰州总医院骨科研究所,甘肃 兰州 730050 Institute of Orthopaedics,Lanzhou General Hospital of PLA,Lanzhou 730050,Gansu,China chkeming@yahoo.com.cn 
期刊信息:《中国骨伤》2012年25卷,第11期,第931-936页
DOI:10.3969/j.issn.1003-0034.2012.11.013
基金项目:甘肃省科技重大专项资助项目(编号:09ZNKDA025)


目的:研究静磁场不同处理时间对体外培养成骨细胞增殖与分化成熟的影响.

方法:原代培养大鼠颅骨成骨细胞,传代后随机分为9组,用磁场强度为3.9 mT的静磁场,分别处理0(对照组)、0.5、1.0、1.5、2.0、2.5、3.0、3.5、4.0 h.倒置相差显微镜下观察细胞形态;48 h后检测细胞增殖情况;第3、6、9、12天测定碱性磷酸酶活性和钙盐沉积量;第8天进行碱性磷酸酶染色;第10天进行茜素红钙化结节染色;在SMFs(static magnetic fields)处理0、24、48、72 h后,Real-time PCR检测骨形态发生蛋白(bone morphogenetic protein-2,BMP-2),Runx-2,骨保护素(osteoprotegerin,Opg)的mRNA表达水平变化.

结果:与对照组相比,磁场组均促进细胞增殖(P<0.01或P<0.05),也能明显促进其分化成熟,表现为提高细胞的ALP 活性,促进钙盐沉积量,提高BMP-2、Runx-2和Opg的mRNA表达.

结论:磁感应强度为3.9 mT的静磁场处理体外培养成骨细胞2.5 h时,其对成骨细胞的增值与分化效果最为明显.
[关键词]:成骨细胞  电磁场  细胞增殖  细胞分化
 
Effects of static magnetic field at different times on the proliferation and differentiation of osteoblasts in vitro
Abstract:

Objective:To investigate the effect of exposure to static magnetic fields (SMFs) of 3.9 mT on proliferation and differentiation of osteoblasts in vitro.

Methods:The newborn rat calvarial osteoblasts were isolated by enzyme digestion and randomly divided into 9 groups after one passage. The intensity of the SMFs was 3.9 mT. The cells were exposed in the SMFs for 0 (control group),0.5,1.0,1.5,2.0,2.5,3,3.5 and 4.0 h groups respectively. They were observed under the contrast phase microscope each day. After 48 h,cell proliferation was assayed by MTT method. The alkaline phosphatase (Alkaline Phosphatase,ALP) activities and calcium content were measured after 3,6,9,and 12 days exposed with SMFs. The ALP positive colonies were histochemically stained after 8 days and the calcified nodules were stained by Alizarin Bordeaux after 10 days; BMP-2,Runx-2 and Opg mRNA expression were measured after SMFs treatment in 0,24,48 and 72 h.

Results:Contrast with control group,all SMFs groups enhanced cell proliferation (P<0.01 or P<0.05),and they promoted maturation and mineralization of the osteoblasts. The results showed that SMFs improved the ALP activity,promoted calcium content,boost BMP-2,Runx-2 and Opg mRNA expression.

Conclusion:The cells exposed to the SMFs of 3.9 mT at 2.5 h apparently promote proliferation and differentiation of osteoblasts in vitro.
KEYWORDS:Osteoblasts  Electromagnetic fields  Cell proliferation  Cell differentiation
 
引用本文,请按以下格式著录参考文献:
中文格式:王嘉琪,葛宝丰,马晓妮,周建,郭晓宇,陈克明.静磁场不同处理时间对体外培养成骨细胞增殖与分化的影响[J].中国骨伤,2012,25(11):931~936
英文格式:WANG Jia-qi,GE Bao-feng,MA Xiao-ni,ZHOU Jian,GUO Xiao-yu,CHEN Ke-ming.Effects of static magnetic field at different times on the proliferation and differentiation of osteoblasts in vitro[J].zhongguo gu shang / China J Orthop Trauma ,2012,25(11):931~936
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