Suppr超能文献

[利用尿液细胞建立血友病A患者特异性诱导多能干细胞]

[Establishment of hemophilia A patient-specific inducible pluripotent stem cells with urine cells].

作者信息

Hu Zhiqing, Hu Xuyun, Pang Jialun, Wang Xiaolin, Lin Peng Siyuan, Li Zhuo, Wu Yong, Wu Lingqian, Liang Desheng

机构信息

State Key Laboratory of Medical Genetics, Central South University, Changsha, Hunan 410078, P.R. China. Email:

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Oct;32(5):609-14. doi: 10.3760/cma.j.issn.1003-9406.2015.05.001.

Abstract

OBJECTIVE To generate hemophilia A (HA) patient-specific inducible pluripotent stem cells (iPSCs) and induce endothelial differentiation. METHODS Tubular epithelial cells were isolated and cultured from the urine of HA patients. The iPSCs were generated by forced expression of Yamanaka factors (Oct4, Sox2, c-Myc and Klf4) using retroviruses and characterized by cell morphology, pluripotent marker staining and in vivo differentiation through teratoma formation. Induced endothelial differentiation of the iPSCs was achieved with the OP9 cell co-culture method. RESULTS Patient-specific iPSCs were generated from urine cells of the HA patients, which could be identified by cell morphology, pluripotent stem cell surface marker staining and in vivo differentiation of three germ layers. The teratoma experiment has confirmed that such cells could differentiate into endothelial cells expressing the endothelial-specific markers CD144, CD31 and vWF. CONCLUSION HA patient-specific iPSCs could be generated from urine cells and can differentiate into endothelial cells. This has provided a new HA disease modeling approach and may serve as an applicable autologous cell source for gene correction and cell therapy studies for HA.

摘要

目的 生成血友病A(HA)患者特异性诱导多能干细胞(iPSC)并诱导其向内皮细胞分化。方法 从HA患者尿液中分离并培养肾小管上皮细胞。使用逆转录病毒通过强制表达山中因子(Oct4、Sox2、c-Myc和Klf4)来生成iPSC,并通过细胞形态、多能性标志物染色以及通过畸胎瘤形成进行体内分化来进行表征。采用OP9细胞共培养方法实现iPSC的诱导内皮分化。结果 从HA患者的尿液细胞中生成了患者特异性iPSC,可通过细胞形态、多能干细胞表面标志物染色以及三个胚层的体内分化来鉴定。畸胎瘤实验证实,此类细胞可分化为表达内皮特异性标志物CD144、CD31和vWF的内皮细胞。结论 可从尿液细胞中生成HA患者特异性iPSC,且其可分化为内皮细胞。这为HA疾病建模提供了一种新方法,并可能作为HA基因校正和细胞治疗研究的适用自体细胞来源。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验