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作 者:肖新华[1] 周后德[1] 王运林[2] 张红[1] 袁凌青[1] 胡平安[1] 杨雅[1] 何玉玲[1] 隋国良[1] 翟木绪[1] 王敏[1] 廖二元[1]
机构地区:[1]中南大学湘雅二医院代谢内分泌研究所,长沙410011 [2]华中科技大学同济医院综合科
出 处:《中国骨质疏松杂志》2005年第2期151-155,共5页Chinese Journal of Osteoporosis
基 金:国家自然科学基金资助项目(30400218)
摘 要:目的观察小鼠的单核/巨噬细胞RAW264.7的一般生物学特征及在RANKL诱导下形成成熟破骨细胞的特征。方法 RANKL诱导RAW264.7细胞6d后,用抗酒石酸酸性磷酸酶(TRAP) 染色法观察TRAP阳性多核细胞,吖啶橙染色激光共聚焦显微镜(LCSM)观察多核细胞形态;诱导RAW264.7细胞9d后,RT-PCR检测RAW264.7细胞的破骨细胞表型和功能基因表达及其 RANKL诱导后变化;诱导RAW264.7细胞12d后,钙磷覆盖的破骨细胞活性分析板观察破骨细胞的骨吸收功能。结果 RAW264.7细胞TRAP染色阴性,单核或2个核,能表达破骨细胞表型和功能基因,无骨吸收功能。RANKL可诱导RAW264.7细胞形成TRAP阳性成熟的多核破骨细胞, 上调CathepsinK、CAⅡ、integrinβ3等基因。mRNA的表达。结论 RAW264.7具有破骨细胞特征性基因表达谱,是一种较好的破骨前体细胞模型。RANKL可诱导RAW264.7细胞形成成熟破骨细胞。Objective To observe the biologic characteristics of RAW264. 7 cell, monocyte/macro-phage cell origined from mouse, and to study the characteristics of mature osteoclast induced by RANKL from RAW264. 7. Methods RAW264. 7 cells were treated with or without RANKL for 6 days, and the morphological change was observed after TRAP staining and by LCSM. Osteoclast phenotypic and functional genes were detected with semiquantitative RT-PCR when RAW264. 7 cells were induced for 9 days. Osteoclastic absorption functions were evaluated by bone resorption pit formation on osteoclast activity analysis platelet when RAW264. 7 cells were induced for 12 days. Results RAW264. 7 cells show TRAP-negative with monocyte or 2 nucleus, expressing osteoclast phenotypic and functional genes without capability of absorbing bone tissue. RAW264. 7 cells could be induced to mature multiple nucleus osteoclasts, The expression of cathepsin K, CAII, integrin β 3 mRNA could be up - regulated by RANKL. Conclusions RAW264. 7 cell could be used as a preferable preoste-oclast model in respect of its osteoclast characteristic gene expression profile. RANKL could induce RAW264. 7 cell to mature osteoclast.
关 键 词:成熟破骨细胞 RANKL RAW264.7细胞 单核细胞 小鼠 抗酒石酸酸性磷酸酶 激光共聚焦显微镜 integrin 单核/巨噬细胞 骨吸收功能 分化 TRAP 多核破骨细胞 基因mRNA 细胞表型 细胞形成 生物学特征 吖啶橙染色 基因表达及
分 类 号:R336[医药卫生—人体生理学] R783.5[医药卫生—基础医学]
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