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过表达人肝细胞生长因子的人毛囊间充质干细胞的建立

Establishment of human hair follicle mesenchymal stem cells with overexpressed human hepatocyte growth factor.

作者信息

Zhou Dan, Cheng Hongjing, Liu Jinyu, Zhang Lei

机构信息

Department of Pediatrics, The Second Hospital of Jilin University, Changchun 130041, China.

Department of Gastroenterology, The First Hospital of Jilin University, Changchun 130041, China.

出版信息

Iran J Basic Med Sci. 2017 Jun;20(6):662-675. doi: 10.22038/IJBMS.2017.8834.

DOI:10.22038/IJBMS.2017.8834
PMID:28702144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5501929/
Abstract

OBJECTIVES

Chronic liver disease has become a major health problem that causes serious damage to human health. Since the existing treatment effect was not ideal, we need to seek new treatment methods.

MATERIALS AND METHODS

We utilized the gene recombination technology to obtain the human hair mesenchymal stem cells which overexpression of human hepatocyte growth factor (hHGF). Furthermore, we verified the property of transfected cells through detecting surface marker by flow cytometry.

RESULTS

We show here establishment of the hHGF-overexpressing lentivirus vector, and successfully transfection to human hair follicle mesenchymal stem cells. The verified experiments could demonstrate the human hair follicle mesenchymal stem cells which have been transfected still have the properties of stem cells.

CONCLUSION

We successfully constructed human hair follicle mesenchymal stem cells which overexpression hHGF, and maintain the same properties compared with pro-transfected cells.

摘要

目的

慢性肝病已成为严重损害人类健康的主要健康问题。由于现有治疗效果不理想,我们需要寻找新的治疗方法。

材料与方法

我们利用基因重组技术获得过表达人肝细胞生长因子(hHGF)的人毛囊间充质干细胞。此外,我们通过流式细胞术检测表面标志物来验证转染细胞的特性。

结果

我们在此展示了hHGF过表达慢病毒载体的构建,并成功转染到人毛囊间充质干细胞。验证实验可以证明已转染的人毛囊间充质干细胞仍具有干细胞特性。

结论

我们成功构建了过表达hHGF的人毛囊间充质干细胞,且与转染前细胞相比保持相同特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/c2cce7d70b3c/IJBMS-20-662-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/4dc80d831adc/IJBMS-20-662-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/d5eee2d0a239/IJBMS-20-662-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/a7da1e15767e/IJBMS-20-662-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/22a07cebdad8/IJBMS-20-662-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/c2cce7d70b3c/IJBMS-20-662-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/4dc80d831adc/IJBMS-20-662-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/22a07cebdad8/IJBMS-20-662-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/2cd96cafcbd1/IJBMS-20-662-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/1df3603b01e9/IJBMS-20-662-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/a75861c68493/IJBMS-20-662-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/7db2bf93601c/IJBMS-20-662-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/7fd754b910f0/IJBMS-20-662-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/c21efc4eebe2/IJBMS-20-662-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/c784e70530b2/IJBMS-20-662-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/3f7429d9695b/IJBMS-20-662-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/5ed3fed6a778/IJBMS-20-662-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/6cb02aaba868/IJBMS-20-662-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/4f3faede7a8a/IJBMS-20-662-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/ab7f58c1188f/IJBMS-20-662-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c8/5501929/c2cce7d70b3c/IJBMS-20-662-g020.jpg

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New Tools in Experimental Cellular Therapy for the Treatment of Liver Diseases.用于治疗肝脏疾病的实验性细胞疗法中的新工具
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