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作 者:段德宇[1] 杨述华[1] 吴星火[1] 张志才[1] 陈超[1] 苏正兵[1] 方为志[1]
机构地区:[1]华中科技大学同济医学院附属协和医院骨科,武汉430022
出 处:《中华实验外科杂志》2013年第7期1339-1342,共4页Chinese Journal of Experimental Surgery
基 金:武汉市科技攻关计划资助项目(201161038340-04)
摘 要:目的观察脐带静脉内皮细胞(HUVEC)诱导去分化重编排脂肪干细胞成骨分化的效果并探讨其分子机制。方法分离人脂肪干细胞(hASCs),取第3代hASCs进行去分化重编排并标记为去分化重编排脂肪干细胞(De.hASCs)。分离人HUVEC,将hASCs与HUVEC以1:1比例进行共培养(hASCs组),将De—hASCs与HUVEC以1:1比例进行共培养(De—hASCs组)。并于共培养4d和7d后检测碱性磷酸酶(ALP)活性,Runt相关基因2(Runx2)和骨形态发生蛋白-2(BMP-2)的mRNA表达水平,骨钙素的mRNA表达水平。结果共培养4d后,De—hASCs组的ALP活性高于hASCs组,但差异无统计学意义(P〉0.05)。共培养7d后,De—hASCs组ALP活性高于hASCs组,且差异有统计学意义(P〈0.05)。共培养4d和7d后,De—hASCs组Runx2和BMP一2的mRNA表达水平均明显高于hASCs组,且差异有统计学意义(P〈0.05)。共培养4d和7d后,De-hASCs组骨钙素的mRNA表达水平高于hASCs组,但差异无统计学意义(P〈0.05)。结论去分化重编排hASCs与HUVEC共培养条件下具有比普通脂肪干细胞更强的成骨分化能力,且与其上调BMP一2基因表达相关。Objective To study the osteogenic differentiation and related molecular mechanisms of dedifferentiation reprogrammed hASCs (De-hASCs) induced by human umbilical vein endothelial cells (HUVECs). Methods HASCs were isolated from 6 volunteers. HASCs passaged three times were then selected to undergo the dedifferentiation reprogrammed process. These cells were denoted as the De-hASCs. Both De-hASCs and hASCs were then co-cultured with HUVECs for a total period of one week. Alkaline phosphatase (ALP) activity of cells cultured for 4 and 7 days were measured, runt related tran- scription factor-2 ( Runx2 ) and bone morphogenetic protein-2 (BMP-2) mRNA levels of cells cultured for 4 and 7 days were detected. Osteocalcin mRNA expression levels of cells cultured for 4 and 7 days were ex- amined. Results ALP activity of the De-hASCs measured 4 days after cell culture was stronger than that of hASCs, but there was no significant difference. ALP acitivty of the De-hASCs measured 7 days after cell culture was stronger than that of hASCs with significant difference. Runx2 and BMP-2 mRNA expression levels of the De-hASCs were higher than those of hASCs both 4 and 7 days after cell culture with siginificant difference. Osteocalcin mRNA expression levels of De-hASCs were higher than those of hASCs both 4 and 7 days after cell culture but without significant difference. Conclusion When co-cultured with HUVECs, De-hASCs possessed a stronger osteogenic differentiation capacity than hASCs by up-regulating the expres- sion of BMP-2.
关 键 词:去分化重编排 成骨分化 脂肪干细胞 脐带静脉内皮细胞 共培养
分 类 号:R329.2[医药卫生—人体解剖和组织胚胎学]
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