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靶向脐带间充质干细胞的构建及其在小鼠脾脏内的定位
引用本文:秦力维,张宁坤,路平,彭秀军,王桂琴,高原,曹利群,崔蓓,郭建巍.靶向脐带间充质干细胞的构建及其在小鼠脾脏内的定位[J].中国比较医学杂志,2015,25(6):32-35.
作者姓名:秦力维  张宁坤  路平  彭秀军  王桂琴  高原  曹利群  崔蓓  郭建巍
作者单位:海军总医院 眼科, 北京 100048;海军总医院 心脏中心, 北京 100048;海军总医院 病理科, 北京 100048;海军总医院 眼科, 北京 100048;海军总医院 眼科, 北京 100048;海军总医院 眼科, 北京 100048;海军总医院 眼科, 北京 100048;海军总医院 眼科, 北京 100048;海军总医院 检验科, 北京 100048
基金项目:国家自然科学基金(30872394)及海军总医院创新培育基金资助(CXPY201312)。
摘    要:目的 构建含小分子肽P1-GFP融合基因慢病毒载体, 用携带P1-GFP融合基因的慢病毒感染MSC, 使MSC具有靶向性, 将靶向MSC注入小鼠体内后观察MSC在小鼠脾脏的定位及与淋巴细胞的关系。方法 用组织片贴壁法培养健康人脐带间充质干细胞, 用基因工程技术构建含小分子肽P1-GFP融合基因慢病毒载体并感染人脐带间充质干细胞, 通过尾静脉将转入P1-GFP融合基因的MSC注入小鼠体内, 18 h后免疫组化染色观察GFP在小鼠脾脏的定位。 结果 培养的健康人脐带间充质干细胞生长良好, MSC感染含P1-GFP融合基因的慢病毒18 h后MSC开始出现绿色荧光, 随着培养时间的延长, 荧光强度逐渐增强, 72 h达高峰。靶向MSC表达髓系干细胞的表面标记 CD105(90.0%)/CD44(98%),CD73(85.0%)/CD90(98.5%)。将靶向MSC经尾静脉注入小鼠体内, 18 h后小鼠脾脏出现大量GFP阳性细胞, 并与脾脏淋巴细胞密切接触。结论 本研究成功构建了含P1-GFP融合基因的靶向MSC, 靶向MSC成功定向脾脏, 并与脾脏淋巴细胞密切接触, 可用于后续的实验研究。

关 键 词:靶向  脐带间充质干细胞  慢病毒  脾脏
修稿时间:2015/4/25 0:00:00

Construction of targeted umbilical cord derived mesenchymal stem cells and their distribution in the mouse spleen
QIN Li-wei,ZHAMG Ning-kun,LU Ping,PENG Xiu-jun,WANG Gui-qin,GAO Yuan,CAO Li-qun,CUI Bei and GUO Jian-wei.Construction of targeted umbilical cord derived mesenchymal stem cells and their distribution in the mouse spleen[J].Chinese Journal of Comparative Medicine,2015,25(6):32-35.
Authors:QIN Li-wei  ZHAMG Ning-kun  LU Ping  PENG Xiu-jun  WANG Gui-qin  GAO Yuan  CAO Li-qun  CUI Bei and GUO Jian-wei
Institution:Department of Ophthalmology, Chinese PLA Navy General Hospital, Beijing 100048, China;Heart Center, Chinese PLA Navy General Hospital, Beijing 100048, China;Department of Pathology, Chinese PLA Navy General Hospital, Beijing 100048, China;Department of Ophthalmology, Chinese PLA Navy General Hospital, Beijing 100048, China;Department of Ophthalmology, Chinese PLA Navy General Hospital, Beijing 100048, China;Department of Ophthalmology, Chinese PLA Navy General Hospital, Beijing 100048, China;Department of Ophthalmology, Chinese PLA Navy General Hospital, Beijing 100048, China;Department of Ophthalmology, Chinese PLA Navy General Hospital, Beijing 100048, China;Department of Clinical Laboratory, Chinese PLA Navy General Hospital, Beijing 100048, China
Abstract:Objective To construct lentiviral vectors containing peptide P1-GFP fusion genes. Umbilical cord derived mesenchymal stem cells were infected with lentivirus carrying peptide P1 and GFP fusion genes. To inject the targeted umbilical cord derived mesenchymal stem cells into mice and to detect GFP expression in the spleen. Methods Umbilical cord derived mesenchymal stem cells were cultured with adhered tissues of umbilical cord smaller than 1 mm3. Lentiviral vector containing P1-GFP fusion genes with engineering technology was constructed and infected the umbilical cord derive mesenchymal stem cells. Targeted umbilical cord derived mesenchymal stem cells were intravenously injected in the mouse tail vein and after 18 hours GFP expression was detected with immunohistochamical staining of the spleen tissues. Results Harvested umbilical cord derived mesenchymal stem cells grew well in culture medium. Green fluorescence on umbilical cord derived mesenchymal stem cells were observed under fluorescence microscope at 18 hours after infected with lentivirus. Green fluorescence intensity of umbilical cord derived mesenchymal stem cells was increasing over time and reached a peak at 72 hours. Umbilical cord derived mesenchymal stem cells highly expressed CD105 (90.0%)/CD44 (98%) and CD73 (85.0%)/CD90 (98.5%) molecules. GFP expression was detected in the spleen after intravenous injection of targeted umbilical cord derived mesenchymal stem cells in the mice 18 hours later. GFP expressing cells intimately contacted with lymphocytes. Conclusions Targeted umbilical cord derived mesenchymal stem cells contain P1-GFP fusion genes are constructed. Targeted umbilical cord derived mesenchymal stem cells can be targeted to mouse spleen and intimately contact with lymphocytes after intravenous injection. Our results lay the groundwork for further studies.
Keywords:Targeted umbilical cord derived mesenchymal stem cells  Lentivirus  Spleen  Mice
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