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作 者:陈海英[1,2] 高连如[1] 张宁坤[1] 杨明[3] 王志国[1]
机构地区:[1]海军总医院心脏中心,北京100048 [2]解放军第210医院内分泌科,辽宁大连116021 [3]海军总医院检验科,北京100048
出 处:《现代生物医学进展》2012年第4期645-648,共4页Progress in Modern Biomedicine
基 金:国家863计划资助课题(No:2006AA02Z469)
摘 要:目的:诱导脐带华通胶间充质干细胞向Flk1阳性细胞分化。方法:胶原酶法分离培养脐带华通胶间充质干细胞,第3代细胞以含2-巯基乙醇的分化培养基培养,应用RT-PCR和流式细胞仪从mRNA和蛋白水平检测Flk1阳性细胞分化水平。结果:脐带华通胶间充质干细胞Flk1mRNA及蛋白表达极低,分化培养基培养后表达上调,48h达高峰(P<0.05),之后表达降低。结论:2-巯基乙醇可诱导脐带华通胶间充质干细胞向Flk1阳性细胞分化,为从中分选Flk1阳性细胞进行进一步研究提供了依据。Objective: Induce mesenchymal stem cells from human umbilical cord Wharton’s jelly differentiate into Flk1-positive cells.Methods: Mesenchymal stem cells from human umbilical cord Wharton’s jelly(WJ-MSCs) were isolated by collagenase digestion and passage 3 cells were cultured by differentiation medium contained 2-mercaptoethanol,Flk1 mRNA were examined by RT-PCR,Flk1 protein were analyzed by flow cytometry.Results: Low expression of Flk1 mRNA and Flk1 protein were detected in WJ-MSCs.Flk1 expression increased after cultured by differentiation medium,and reached maximum after 48h culture,then declined.Conclusions: Mesenchymal stem cells from human umbilical cord Wharton’s jelly could be induced and differentiated into Flk1-positive cells by 2-mercaptoethanol,which can be used to select Flk1-positive cells in WJ-MSCs.
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