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作 者:王丽[1,2,3] 范文斌[1,2,3] 吕立夏[1,2,3] 李鹏[1,2,3] 田海滨[1,2,3] 徐国彤[1,2,3]
机构地区:[1]同济大学医学院眼科研究所,上海200092 [2]同济大学医学院再生医学系,上海200092 [3]同济大学医学院干细胞研究中心,上海200092
出 处:《同济大学学报(医学版)》2015年第5期1-7,共7页Journal of Tongji University(Medical Science)
基 金:国家"九七三"重点基础研究发展计划(2013CB967501);国家自然科学基金(C120111)
摘 要:目的探讨采用关键转录因子将人脐带间充质干细胞(human umbilical cord mesenchymal stem cells,h UC-M SCs)转分化为视网膜色素上皮(retinal pigment epithelium,RPE)样细胞的方法。方法通过流式细胞技术鉴定h UC-MSCs的表面标记分子;通过诱导h UC-MSCs分化成为脂肪、骨和软骨细胞确定其多系分化能力;采用慢病毒包装系统获得分别含有11个转录因子Sox2、Pax6、Rax、Six6、Nr2e1、Otx2、Lhx2、Crx、Mitf-A、Klf4和c-Myc的病毒,并通过感染h UC-MSCs来诱导h UC-MSCs向RPE样细胞分化。结果 h UC-MSCs表达CD29、CD44、CD73、CD90和CD105,但不表达CD11b、CD34,CD45和HLA-DR等分子标记,在成脂、成骨、成软骨分化培养基中可分化为脂肪、骨和软骨细胞。视网膜及RPE发育相关的关键转录因子能够将h UC-MSCs直接转分化为RPE样的细胞,并表达ZO-1、RPE65、Bestrophin-1(Best-1)、CK8/18、Cralbp、Mertk、Tyrosinase(Tyr)、PEDF等RPE细胞的特征分子。结论视网膜及RPE发育相关的关键转录因子可直接将h UC-MSCs分化为RPE样细胞。Objective To investigate the transdifferentiation of human umbilical cord mesenchymal stem cells( h UC-M SCc) into retinal pigment epithelial( RPE) cells. Methods M SC specific markers were identified by flowcytometry in h UC-M SCs,and adipogenesis,osteogenesis and chondrogenesis were confirmed by culturing h UC-M SCsin differentiation media. Sox2,Pax6,Rax,Six6,Nr2e1,Otx2,Lhx2,Crx,M itf-A,Klf4 and c-M yc were co-infected into h UC-M SCs by lentivirus-mediated system. The h UC-M SCs derived RPE-like cells were characterized by detecting the expressions of specific markers by real-time quantitative-polymerase chain reaction( Q-PCR),immunostaining and Western blot. Results h UC-M SCs were positive for CD29,CD44,CD73,CD90, CD105 and negative for CD11 b,CD34,CD45,HLA-DR. After induction,h UC-M SCs were differentiate into adipocytes,osteoblasts and chondrocytes. Retina and RPE development related transcription factors directly transdifferentiated h UC-M SCs into RPE-like cells which expressed RPE specific markers ZO-1,RPE65,Bestrophin-1,CK8 /18,Cralbp,M ertk,Tyrosinase and PEDF. Conclusion h UC-M SCs could be directly transdifferentiated into RPE-like cells by key transcription factors.
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