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中国应用生理学杂志 ›› 2017, Vol. 33 ›› Issue (6): 503-507.doi: 10.12047/j.cjap.5601.2017.120

• 研究论文 • 上一篇    下一篇

致心律失常性右室心肌病患者的诱导性多能干细胞系的建立

蒋彬, 王国卿, 李红霞, 蒋文平, 陈涛, 姜岩   

  1. 苏州大学, 江苏 苏州 215123
  • 收稿日期:2016-07-13 修回日期:2017-05-18 出版日期:2017-11-28 发布日期:2018-06-19
  • 基金资助:
    国家自然科学基金项目(81300143);中国博士后基金(2013M541718)

Generation of induced pluripotent stem cells from arrhythmogenic right ventricular disease patient

JIANG Bin, WANG Guo-qing, LI Hong-xia, JIANG Wen-ping, CHEN Tao, JIANG Yan   

  1. Soochow University, Suzhou 215123, China
  • Received:2016-07-13 Revised:2017-05-18 Online:2017-11-28 Published:2018-06-19
  • Contact: 姜岩,Tel:15950069815,18260195811;E-mail:Yjiang@suda.edu.cn;陈涛,E-mail:Tchen@suda.edu.cn E-mail:Yjiang@suda.edu.cn;Tchen@suda.edu.cn
  • Supported by:
    国家自然科学基金项目(81300143);中国博士后基金(2013M541718)

摘要: 目的:建立致心律失常性右室心肌病(ARVC)患者特异性的诱导性多能干细胞(iPSCs),为研究ARVC发病机制提供研究模型。方法:培养来源于ARVC患者皮肤成纤维细胞,并进行突变位点测序鉴定。通过仙台病毒转导入外源性多能转录因子,将ARVC患者皮肤细胞诱导为iPSCs,结合免疫荧光法,实时荧光定量PCR,以及体内外三胚层形成实验对iPS细胞全能型进行鉴定。通过调控Wnt信号通路诱导iPS细胞定向分化为心肌细胞。结果:ARVC患者来源的iPSCs显示碱性磷酸酶阳性,多能性相关基因高表达,胚胎干细胞标志物Oct4,SSEA4,TRA-1-81阳性。体外悬浮培养形成的拟胚体以及体内畸胎瘤形成实验均显示ARVC-iPSCs具有向3个胚层分化能力。经过体外心肌定向,ARVC-iPSC可诱导产生自主节律性搏动细胞团,免疫荧光显示cTnT阳性。结论:本研究使用仙台病毒,建立了无插入型ARVC患者特异的诱导性多能干细胞系,该细胞系具有多能分化特性,并可定向分化为心肌细胞,为研究ARVC的致病因素和药物筛选提供宝贵的实验模型。

关键词: 致心律失常性右室心肌病, 诱导性多能干细胞, 心肌定向分化

Abstract: Objective: To establish the induced pluripotent stem cells (iPSCs) from patients with arrhythmogenic right ventricular cardiomyopathy (ARVC).Methods: The fibroblasts were isolated from ARVC patient and DNA mutation sites were confirmed. We reprogrammed the patient fibroblasts to pluripotency by sendaiviral transduction with defined pluripotency factors. Then, we evaluated the pluripotency of ARVC-iPSCs by performing the immunofluorescence analysis, real-time PCR and 3 germ layer formation assay. We also induced the ARVC-iPSCs into cardiac specific differentiation by regulating Wnt signaling pathway.Results: Apart from alkaline phosphatase positive staining, iPSCs derived from ARVC patients expressed pluripotent related genes and embryonic stem cell marker OCT4, SSEA4 and TRA-1-81. Embryonic body formation in vitro and teratoma test in vivo demonstrated that ARVC-iPSCs could differentiate into all three germ layers. After in vitro cardiac differentiation, ARVC-iPSC could be successfully induced to spontaneously beating mass with cTNT staining positive.Conclusion: Induced pluripotent stem cell was successfully established by integration free sendai virus from dermal fibroblast of patients with ARVC. It would provide the valuable experimental model to study the molecular mechanism of ARVC.

Key words: arrhythmogenic right ventricular cardiomyopathy, induced pluripotent stem cells, cardiac differentiation

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