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机构地区:[1]南京军区南京总医院输血科,江苏南京210002 [2]南京医科大学,江苏南京210029
出 处:《中国血液流变学杂志》2013年第3期413-415,共3页Chinese Journal of Hemorheology
基 金:南京军区医学科技创新重点项目(112026),南京军区南京总医院科研基金(2011048,2011050)
摘 要:目的探讨定向诱导造血干细胞分化为巨核细胞和血小板的分子机制。方法将脐带造血干细胞培养后,分离巨核细胞,分别提取造血干细胞和巨核细胞总RNA,进行microRNA芯片分析。结果与造血干细胞相比,巨核细胞中表达上调超过2倍的microRNA有183个,下调超过2倍的microRNA有139个。结论造血干细胞和巨核细胞microRNA表达谱存在差异,尤其是多个microRNA与定向分化巨核细胞相关。Abstract: Objective To elucidate the mechanism of megakaryocyte development and platelet production from hematopoietic stem cells. Methods CD34+ cells were isolated from umbilical cord blood and cultivated. Megakaryocytes were purified from cultivated CD34+ cells.Total RNAs from CD34+ cells and megakaryocytes were extracted.Microarray analysis was performed to determine differential expressed microRNAs.Results Differential microRNAs were defined as a statistically significant difference with 2 fold or greater change. Compared with hematopoietic stem cells,183 microRNAs showed higher expression and 139 microRNAs were down-regulated in megakaryocytes.Conclnsion The differential expressed microRNAs between hematopoietic stem cells and megakaryocytes indicates that some microRNAs play an important role in regulating megakaryocytes differentiation from hematopoietic stem cells.
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