[1]孙一,李大伟,张海宁.hIGF-1基因改良修饰人脐血间充质细胞的研究[J].中华老年骨科与康复电子杂志,2018,(06):346-351.[doi:10.3877/cma.j.issn.2096-0263.2018.06.006]
　Sun Yi,Li Dawei,Zhang Haining.The study on modification of human umbilical cord blood mesenchymal cells by hIGF-1 gene[J].Chin J Geriatr Orthop Rehabil(Electronic Edition),2018,(06):346-351.[doi:10.3877/cma.j.issn.2096-0263.2018.06.006]
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hIGF-1基因改良修饰人脐血间充质细胞的研究()
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中华老年骨科与康复电子杂志[ISSN:1674-3911/CN:11-9292/R]

卷:
期数:
2018年06期
页码:
346-351
栏目:
基础研究
出版日期:
2018-11-23

文章信息/Info

Title:
The study on modification of human umbilical cord blood mesenchymal cells by hIGF-1 gene
作者:
孙一; 李大伟; 张海宁
266000 青岛大学附属医院关节外科
Author(s):
Sun Yi;  Li Dawei;  Zhang Haining
Department of Joint Surgery, the Affiliated Hospital of Qingdao University, Qingdao 266000, China
关键词:
胰岛素样生长因子1;  脂质体;  间充质干细胞;  基因转染
Keywords:
Insulin-like growth factor 1;  Liposomes;  Gene transfection;  Mesenchymal stem cells
DOI:
10.3877/cma.j.issn.2096-0263.2018.06.006
文献标志码:
A
摘要:
目的 研究hIGF-1基因改良修饰人脐血间充质干细胞的方法，为关节软骨组织工程修复提供良好的种子细胞。方法 综合应用密度梯度离心法和细胞贴壁法分离培养人脐血间充质干细胞，流式细胞仪进行细胞鉴定。通过X-tremen HP介导将含hIGF-1基因全长的真核表达载体pIRES2-EGFP-hIGF-I转染人脐血间充质干细胞，倒置荧光显微镜检测转染后荧光蛋白的表达，计算转染效率，ELISA检测转染后细胞上清液中hIGF-1的含量变化，免疫荧光与RT-PCR检测hIGF-1在细胞中的表达，免疫组化检测Ⅱ型胶原表达。结果 人脐血间充质干细胞表面表达CD105（99.93%）、CD90（99.85%）、CD146（73.63%），不表达Anti-HLA-DR（1.38%）、CD45（0.13%）、CD34（0.11%）。hIGF-1基因可在X-tremen HP介导下转染人脐血间充质干细胞，48 h转染效率为（29±8）%。转染后48 h分泌的hIGF-1最多，为（34.89±0.38）ng/ml，且与对照组相比，差异具有统计学意义（P＜0.01）。转染后细胞可检测到hIGF-1 mRNA、蛋白以及Ⅱ型胶原表达。结论 hIGF-1基因可通过X-tremen HP介导改良修饰人脐血间充质干细胞，促进hIGF-1和Ⅱ型胶原的表达与分泌。
Abstract:
Objective To study the modification of human umbilical cord blood mesenchymal stem cells (hUCB-MSCs) by hIGF-1 gene, and provide good seed cells for tissue engineering repair of articular cartilage. Methods hUCB-MSCs were isolated and cultured by density gradient centrifugation and cell adherence method, and cell identification was performed by flow cytometry. The eukaryotic expression vector, pIRES2-EGFP-hIGF-I, containing the full length of hIGF-1 gene was transfected into hUCB-MSCs via X-tremen HP. After transfection, the expression of fluorescent protein was detected by reverse fluorescence microscope and the transfection efficiency was calculated. ELISA was used to detect the content of hIGF-1 in the cell supernatant after transfection, and the immunofluorescence and RT-PCR were used to detect hIGF-1 in the hUCB-MSCs. The expression of the typeⅡ collagen was detected by immunohistochemistry. Results Flow cytometry showed that the hUCB-MSCs expressed CD90, CD105 and CD146 positively, and CD34, CD45, Anti-HLA-DR negatively. hIGF-1 gene was introduced into hUCB-MSCs with X-treme GENE HP DNA transfection reagent, and the transfection efficiency is (29+8)%. The hIGF-1 protein concentration in the supernatants determined by ELISA had significant difference between transfection group and control group (P<0.01). ELISA result showed that the hIGF-1 protein concentration in the supernatants determined after transfection at high level [(35±0.4)ng/ml] at 48 h point. The expression of hIGF-1 was detected by immunofluorescence and RT-PCR identification. Immunohistochemistry showed positive expression of type Ⅱcollagen after transfection. Conclusions hIGF-1 gene can modify human umbilical cord blood mesenchymal stem cells through X-tremen HP mediated modification, and promote the expression and secretion of hIGF-1 and type Ⅱ collagen.

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备注/Memo

备注/Memo:
基金项目：国家自然科学基金（81672197）
更新日期/Last Update: 2018-11-23