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作 者:高杰[1,2] 韩建伟[2] 关凯[1] 杨彤涛[2] 李放[1]
机构地区:[1]北京军区总医院骨科,北京100700 [2]第四军医大学唐都医院骨科,陕西西安710038
出 处:《现代生物医学进展》2013年第30期5855-5859,共5页Progress in Modern Biomedicine
基 金:国家自然科学基金面上项目(81072194)
摘 要:目的:研究miRNAs在人骨髓来源间充质干细胞软骨诱导分化过程中的表达情况。方法:以从骨髓中分离培养的MSCs及软骨诱导培养后的细胞为实验对象,利用基因芯片检测miRNAs的表达情况,由SAM分析得到MSCs较其诱导培养细胞中差异表达的miRNAs,再进行生物信息学分析。结果:①分离培养出的MSCs经软骨诱导培养21天后,已具有软骨细胞特性,经芯片检测并SAM分析,软骨诱导培养的细胞较MSCs高表达的miRNAs有6个:hsa-miR-572、hsa-miR-130b、hsa-miR-193b、hsa-miR-28、hsa-miR-152、hsa-miR-560;软骨诱导培养的细胞较MSCs低表达的miRNAs有2个:hsa-miR-424、hsa-miR-122a。②利用TargetScan预测其靶基因,并行生物信息学分析,其中hsa-miR-130b、hsa-miR-193b、hsa-miR-152及hsa-miR-424的预测靶基因中多为参与细胞分化、骨形成、软骨形成及干细胞表型相关的基因。结论:hsa-miR-130b、hsa-miR-193b、hsa-miR-152和hsa-miR-424等对人骨髓来源间充质干细胞的软骨分化起着重要调控作用。Objective: To identify miRNA expression during chondrogenic differentiation of human bone marrow-derived mesenchymal stem cells. Methods: MSCs were isolated by density centrifugation from bone marrow, and induced to differentiate into chondroblast. miRNA expression in MSCs and chondroblast cells was tested by miRNA microarray with single-channel fluorescence chip and analyzed using SAM software. The potential targets of the miRNAs were analyzed by bioinformatics. Results: MSCs were isolated from bone marrow and induced to differentiate into chondroblast in vitro and miRNA expression of MSCs and chondroblast were investigated using microarrays. Upon differentiation, 6 miRNAs(hsa-miR-572, hsa-miR-130b, hsa-miR-193b, hsa-miR-28, hsamiR-152, and hsa-miR-560) were up-regulated and 2 miRNAs(hsa-miR-424 and hsa-miR-122a) were down-regulated. Among the potential targets, several genes have been evidenced to play a role in osteogenic or chondrogenic differentiation and stemness maintaining. Conclusion: These finding indicate that miRNAs are likely important regulators for chondrogenic differentiation of MSCs.
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