实验动物与比较医学 ›› 2012, Vol. 32 ›› Issue (2): 105-110.DOI: 10.3969/j.issn.1674-5817.2012.02.005

• 论著 • 上一篇    下一篇

西藏小型猪骨髓间充质干细胞分离培养及慢病毒载体介导EGFP标记间充质干细胞

唐华1, 毕文浩2, 艾威2, 李德胜2, 潘光辉2, 史俊文3, 刘薇1, 黄威1, 肖东1, 顾为望1   

  1. 1.南方医科大学比较医学研究所暨实验动物中心, 广州 510515;
    2.广州医学院第二附属医院肾移植科, 广州 510260;
    3.南方医科大学肿瘤研究所, 广州 510515
  • 收稿日期:2011-12-05 出版日期:2012-04-25 发布日期:2012-04-25
  • 作者简介:唐华(1984-),男,硕士研究生,研究方向:干细胞与再生医学,E-mail:huacinth-t@163.com
  • 基金资助:
    广东省医学科学技术研究基金(A2007359)、南方医科大学优秀中青年科技人才库科研资助金和广州地区科学仪器协作共用网专用基金(2006176)、广东省科技计划项目(2009B060300009)、广东省科研条件建设项目(1021010200004)、广东省科技计划项目(2010A011200003)、广东省科技计划项目(2011B060300028)

Isolation and Culture of Bone Marrow Mesenchymal Stem Cells (MSCs) of Tibetan miniature pig, and Lentivirus-mediated EGFP Gene Transfer into MSCs

TANG Hua1, BI Wen-hao2, AI Wei2, LI De-sheng2, PAN Guang-hui2, SHI Jun-wen3, LIU Wei1, HUANG Wei1, XIAO Dong1, GU Wei-wang1   

  1. 1. Institute of Comparative Medicine & Center of Experimental Animals, Southern Medical University, Guangzhou 510515, China;
    2. Department of Kidney Transplantation, The Second Affiliated Hospital, Guangzhou Medical College, Guangzhou 510260, China;
    3. Cancer Research Institute, Southern Medical University, Guangzhou 510515, China
  • Received:2011-12-05 Online:2012-04-25 Published:2012-04-25

摘要: 目的 建立一种简便、有效的西藏小型猪骨髓间充质干细胞(BMSCs)体外分离培养及纯化方法,并基于BMSCs建立慢病毒介导的外源基因EGFP体外投递系统。方法 密度梯度离心法分离西藏小型猪BMSCs,差速贴壁法不断纯化,流式细胞仪检测第3代BMSCs CD45、CD90和CD105表达; 此外,用携带EGFP基因的慢病毒转染BMSCs以获得EGFP标记的BMSCs,倒置荧光显微镜下观察感染情况及流式细胞术检测感染效率。结果 ① 密度梯度分离法结合差速贴壁法所获得的细胞经鉴定符合MSCs的特性。② 借助慢病毒高效率将EGFP导入BMSCs,感染效率为84.1%。结论 利用密度梯度分离法结合差速贴壁法可获得高纯度的BMSCs,基于BMSCs建立了慢病毒介导的外源基因体外投递系统。

关键词: 西藏小型猪, 骨髓间充质干细胞(BMSCs), 慢病毒, 增强型绿色荧光蛋白(EGFP)

Abstract: Objective To establish a simple and effective method used to isolate and purify bone marrow mesenchymal stem cells (BMSCs) of Tibetan miniature pigs, and further set up the lentivirus-mediated in vitro gene delivery system for BMSCs of Tibetan miniature pigs. Methods ①MSCs of Tibetan miniature pigs were initially isolated by density gradient centrifugation, followed by purifying MSCs using differential attachment method, and further passage 3 BMSCs of Tibetan miniature pigs were characterized by CD45, CD90 and CD105. ②According to the standard protocol from Invitrogen, lentiviruses carrying EGFP gene were produced, and then infected MSCs, followed by EGFP assay under fluorescent stereo microscope and fluorescence activated cell sorting (FACS) for determining the infecting efficiency. Results BMSCs of Tibetan miniature pigs obtained by the combined use of density gradient centrifugation and differential attachment method were shown to enjoy the characteristics of MSCs. Additionally, the BMSCs of Tibetan miniature pigs were successfully and efficiently infected by lentivirus supernatant, and the infecting efficiency was 84.1%. Conclusion High purified BMSCs of Tibetan miniature pigs can be obtained by the combined use of density gradient centrifugation and differential attachment method, and lentivirus-mediated in vitro gene delivery systems for BMSCs of Tibetan miniature pigs were successfully established.

Key words: Tibetan miniature pigs, Bone marrow mesenchymal stem cells (BMSCs), Lentivirus, Enhanced green fluorescent protein (EGFP)

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