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大鼠骨髓间充质干细胞体外诱导条件下的成骨特性
引用本文:陈东风,黎晖,周健洪,谢瑶,李伊为,杜少辉,张宜,黄洁,徐敏.大鼠骨髓间充质干细胞体外诱导条件下的成骨特性[J].中西医结合学报,2004,2(5):375-378.
作者姓名:陈东风  黎晖  周健洪  谢瑶  李伊为  杜少辉  张宜  黄洁  徐敏
作者单位:1. 广州中医药大学解剖学教研室,广东,广州,510405
2. 中山大学中山医学院解剖学教研室,广东,广州,510080
3. 深圳市中医院内科,广东,深圳,518000
4. 深圳市沙河医院,广东,深圳,518000
5. 深圳市人民医院,广东,深圳,518000
6. 香港浸会大学中医药学院
基金项目:国家自然科学基金,广东省自然科学基金
摘    要:目的:探讨大鼠骨髓间充质干细胞(mesenchymal stem cells,MSCs)在诱导条件下的成骨特性.方法:使用密度梯度法分离成年大鼠骨髓MSCs,以地塞米松、β-甘油磷酸钠、维生素C为成骨诱导剂.结果:形态学表明,MSCs贴壁细胞呈集落生长,有成纤维细胞外观.地塞米松低剂量组诱导7 d后碱性磷酸酶(alkalian phosphatase,ALP)表达明显升高,阳性细胞数为(15.1±2.6)个,而对照组ALP表达较弱,阳性细胞数为(12.0±3.5)个,两组比较P 《0.01.地塞米松成骨诱导剂低剂量组促进MSC成骨,在诱导7d时即出现钙化结节,而对照组未出现;地塞米松低剂量组诱导21 d钙化结节为(9.0±1.7)个,而对照组为(2.0±1.8)个,两组比较P《0.01.结论:低剂量地塞米松成骨诱导剂能诱导MSC向成骨细胞分化,可以为体内骨组织工程提供种子细胞.

关 键 词:干细胞  骨髓  成骨细胞  动物  实验
文章编号:1672-1977(2004)05-0375-04
修稿时间:2003年9月20日

Osteogenesis characteristics of cultured rat mesenchymal stem cells under bone induction condition
CHEN Dong-Feng,LI Hui,ZHOU Jian-Hong,XIE Yao,LI Yi-Wei,DU Shao-Hui,ZHANG Yi,HUANG Jie,XU Min.Osteogenesis characteristics of cultured rat mesenchymal stem cells under bone induction condition[J].Journal of Chinese Integrative Medicine,2004,2(5):375-378.
Authors:CHEN Dong-Feng  LI Hui  ZHOU Jian-Hong  XIE Yao  LI Yi-Wei  DU Shao-Hui  ZHANG Yi  HUANG Jie  XU Min
Institution:Department of Anatomy, Guangzhou University of Traditional Chinese Medicine, Guangzhou, Guangdong Province 510405, China. cdf27212@21cn.com
Abstract:OBJECTIVE: To investigate the osteogenesis characteristics of cultured rat mesenchymal stem cells (MSCs) under bone induction condition. METHODS: MSCs were isolated from adult rat by using density gradient separation method. The osteogenic inducers were compounds of Dexone, beta-glycerophosphate sodium and vitamin C. RESULTS: The MSC attachment formed soon after the seeding and grew into colonies with the appearance of fibroblastic cells. The osteogenic inducer with low dose of Dexone could promote the osteogenic differentiation of MSC. In the group of osteogenic inducer with low dose of Dexone, the expression of alkaline phosphatase (ALP) was remarkably increased after one week's induction, and the number of positive cells was (15.1 +/- 2.6), significantly higher than that of the control group (12.0 +/- 3.5) (P < 0.01). The calcified deposits began to appear in the group of osteogenic inducer with low dose of Dexone after one week's induction and was increased remarkably after three weeks, and the number of calcified deposits was (9.0 +/- 1.7), significantly higher than that of the control group (2.0 +/- 1.8) (P < 0.01). CONCLUSION: MSC can differentiate into osteogenesis by osteogenic induction and may be used to provide seed cells for bone tissue engineering.
Keywords:stem cell myeloid  osteoblasts  animal  laboratory
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