摘要
生产转基因人类胚胎干细胞(胚胎干细胞)存在一定难度,因而其应用研究受到限制。转基因病毒用于临床并不安全,而非病毒DNA研究方法效率也不高且不安全,但基于mRNA的基因操控方法很有效。在这项研究中,我们通过PCR很容易获取大量多种类体外合成的mRNA 。利用流式细胞技术检测不同转染方法的效率,利用生物发光成像系统研究不同基因修饰方法对蛋白质的翻译效率和荧光素酶基因表达动力学的影响。应用免疫荧光研究转染后人胚胎干细胞的多能性,利用体外合成的胰十二指肠同源盒1(PDX1)mRNA来诱导胚胎干细胞分化为胰岛素分泌细胞。我们发现,电穿孔转染法是最有效的方法之一,并产生超过95%多个胚胎干细胞系的基因表达。合成的mRNA结合多聚腺苷酸的尾,上盖和底座类似物比单个mRNA能更有效地转换成蛋白。通过酶消化成单细胞悬液的细胞mRNA转染方式对胚胎干细胞多能性没有影响,且在胚胎干细胞中多种mRNA均可得到高效转染。我们发现PDX-1 mRNA转染能明显改善β细胞相关基因的表达水平与分化的细胞表达胰岛素和C肽。酶联免疫分析法验证胰岛样细胞群胰岛素分泌对葡萄糖刺激的响应。研究结果表明,体外合成的mRNA电穿孔法用于人胚胎干细胞的基因操纵和胚胎干细胞分化成特定的细胞类型非常有用,这一发现将为该方法的临床应用提供参考。
关键词: 基因操纵,基因治疗,人胚胎干细胞,修饰,mRNA合成
Current Gene Therapy
Title:Gene Manipulation of Human Embryonic Stem Cells by In Vitro-Synthesized mRNA for Gene Therapy
Volume: 15 Issue: 4
Author(s): Xiao Li Wang, Li Yu, Yan Ding, Xing Rong Guo, Ya Hong Yuan and Dong Sheng Li
Affiliation:
关键词: 基因操纵,基因治疗,人胚胎干细胞,修饰,mRNA合成
摘要: The difficulty in producing genetically modified human embryonic stem cells (hESCs) limits research on their applications. Virus-based gene transfer is not safe for clinical use, whereas DNAbased non-viral methods are not efficient or safe, and mRNA-based methods are useful for genetic manipulation. In this study, we easily obtained multiple types and large amounts of in vitrosynthesized mRNA by PCR. The efficiency of different transfection methods was studied by flow cytometry. The effect of different mRNA modifications on protein translation efficiency and dynamics of luciferase mRNA expression in hESCs were studied using a bioluminescence imaging system. The pluripotency of hESCs after transfection was studied by immunofluorescence. In vitro-synthesized pancreatic-duodenal homeobox 1 (PDX1) mRNA was used to induce the differentiation of hESCs into insulin-producing cells. We found that electroporation is the most efficient transfection method, and it produces more than 95% transgene expression in multiple hESC lines. Synthesized mRNA with a combination of a polyA tail, cap and base analogues is more efficiently translated into protein in hESCs compared with single-modified mRNA. Transfection of mRNA into hESCs by trypsinizing the cells into single-cell suspensions did not affect their pluripotency, and multiple types of mRNAs can be transfected into hESCs efficiently. We found that PDX-1 mRNA transfection significantly improved the expression level of genes related to beta cells and differentiated cells that express insulin and C-peptide. ELISA analysis validate the insulin secretion of islet-like cell clusters in response to glucose stimulation. Our results indicate that electroporation of in vitro-synthesized mRNA is useful for genetic manipulation of hESCs and differentiation of hESCs into particular cell types, and this finding will pave the way for clinical applications of this method.
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Xiao Li Wang, Li Yu, Yan Ding, Xing Rong Guo, Ya Hong Yuan and Dong Sheng Li , Gene Manipulation of Human Embryonic Stem Cells by In Vitro-Synthesized mRNA for Gene Therapy, Current Gene Therapy 2015; 15 (4) . https://dx.doi.org/10.2174/1566523215666150515144533
DOI https://dx.doi.org/10.2174/1566523215666150515144533 |
Print ISSN 1566-5232 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5631 |
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