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作 者:王国栋[1] 吴少云[1] 韩金祥[2] 王世立[2] 李萍[1]
机构地区:[1]皖南医学院药学系,安徽芜湖241002 [2]山东省医药生物技术研究中心、国家卫生部生物技术药物重点实验室,山东济南250062
出 处:《细胞与分子免疫学杂志》2012年第10期1025-1028,共4页Chinese Journal of Cellular and Molecular Immunology
基 金:国家高技术研究发展计划(863)资助项目(2003AA2Z3532);安徽高校省级自然科学研究项目(KJ2009B154)
摘 要:目的:观察重组人骨形成蛋白-7(rhBMP-7)对小鼠骨髓间充质干细胞(BMSCs)向成骨细胞分化的影响。方法:采用密度梯度离心法分离骨髓,体外培养扩增,获得小鼠骨髓间充质干细胞,贴壁培养至第3代,向培养液中加入rhBMP-7,培养5 d后进行碱性磷酸酶(ALP)染色,ALP活性与骨钙素(OC)含量检测,并用RT-PCR法分析成骨细胞标志基因骨钙素(OC)与Ⅰ型胶原(Col-Ⅰ)表达情况,Western blot法检测Ⅰ型胶原(Col-Ⅰ)蛋白的分泌量。结果:rhBMP-7诱导组的骨髓间充质干细胞的ALP染色强度、ALP活性及OC含量明显升高,OC与Col-Ⅰ的mRNA表达水平以及Col-Ⅰ的蛋白表达水平均明显提高。结论:rhBMP-7可促进体外培养的小鼠BMSCs向成骨细胞方向分化。AIM: To study the effects of recombinant human bone morphogenetic protein-7 (rhBMP-7) on osteo- blast differentiation of murine bone marrow mesenchymal stem cells (BMSCs). METHODS: The BMSCs were collected from murine bone marrow by density gradient centrifugation. Cells were adherent cultured and expanded in vitro. RhBMP-7 was added into the culture medium of the 3rd passage BMSCs. Five days later, we performed alka- line phosphatase (ALP) staining and detected ALP activity and osteocalcin (OC) content. Osteoblast differentiation marker gene including OC and collage Ⅰ (Col-Ⅰ ) were assayed by RT-PCR. Total protein was isolated and the secretion of Col- Ⅰ in the cells was measured by Western blotting. RESULTS: The staining intensity of ALP in the group with rhBMP-7 was stronger than that in the negative control group. ALP activity and OC content of rhBMP-? group were obviously higher than that of the negative control group. The mRNA of OC and Col-Ⅰ and the protein of Col-Ⅰwere highly expressed in the group induced by rhBMP-7. CONCLUSION: RhBMP-7 can induce murine BMSCs to differentiate into osteoblast in vitro.
关 键 词:重组人骨形成蛋白-7 小鼠 骨髓间充质干细胞 成骨分化
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