检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:赵艳威[1] 李宗旻[2] 宋光明[1] 王越[2] 谢文利[1]
机构地区:[1]武警后勤学院药理学教研室,天津300309 [2]武警后勤学院病原生物与免疫学教研室,天津300309
出 处:《中草药》2014年第4期536-540,共5页Chinese Traditional and Herbal Drugs
基 金:国家自然科学基金资助项目(81273520);天津市自然科学基金资助项目(12JCZDJC26300);天津市自然科学基金资助项目(13JCYBJC24400);武警后勤学院科学技术研究项目(WHZ201202)
摘 要:目的探讨植物雌激素葛根素促进人成骨样MG-63细胞分化的分子机制。方法选择兼有2种雌激素受体(estrogen receptor,ER)亚型表达的人成骨样MG-63细胞为研究模型,采用磷酸苯二钠法、ELISA法及小RNA干扰等技术,探讨葛根素对人成骨细胞分化的作用及作用机制。结果葛根素可通过提高MG-63细胞中碱性磷酸酶(ALP)活性和I型胶原蛋白分泌促进成骨细胞分化成熟,该作用可被纯ER阻断剂ICI 182,780完全阻断,应用小RNA干扰技术进一步证实葛根素对成骨细胞ALP活性、I型胶原蛋白分泌的调节作用是由ERα和ERβ共同介导的。结论葛根素对成骨细胞分化的调节是经ER途径,由ERα和ERβ共同介导。Objective To investigate the molecular mechanism for promotion of puerarin on the differentiation in human osteoblast-like MG-63 cells. Methods Human osteoblast-like MG-63 cells containing two estrogen receptor (ER) isoforms were selected as the suitable model for this study. Disodium phenyl phosphate method, enzyme-linked immnosorbent assay (ELISA), and small interfering double-stranded RNAs (siRNA) technologies were performed to investigate the effect of puerarin on the differentiation in human osteoblast-like MG-63 cells and its molecular mechanism. Results The promotion of puerarin on osteoblastic differentiation could be performed by increasing alkaline phosphatase (ALP) activity and type I collagen protein secretion in human osteoblastic MG-63 cells. The above effect of puerarin on osteoblast-derived cells could be completely blocked by ER antagonist ICI 182, 780. Using siRNA technology, it was further demonstrated that the effects of puerarin on ALP activity and type I collagen protein secretion were mediated by both ERα and ERβ. Conclusion The promotion of puerarin on osteoblastic differentiation is through the ER pathway and is mediated via both ER isotypes, ERα and ERβ.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.219