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两种重编程系统诱导人牙源性多潜能干细胞的对比研究

谭小兵 徐静舒 孙贵虎 宋俊呈 戴青原

重庆医学2017,Vol.46Issue(1):90-93,4.
重庆医学2017,Vol.46Issue(1):90-93,4.DOI:10.3969/j.issn.1671-8348.2017.01.021

两种重编程系统诱导人牙源性多潜能干细胞的对比研究

A comparative study of two reprogramming systems for inducing pluripotent stem cells from human dental origin

谭小兵 1徐静舒 1孙贵虎 2宋俊呈 2戴青原2

作者信息

  • 1. 云南省第一人民医院/昆明理工大学附属医院口腔内科,昆明 650032
  • 2. 昆明医科大学第一附属医院心内科,昆明 650032
  • 折叠

摘要

Abstract

Objective To comparatively study the features of two reprogramming systems of induced pluripotent stem cells (iPSCs)from human dental origin.Methods Two kinds of reprogramming system,i.e.STEMCCA lentivirus /feed layer and Sen-dai virus /matrigel were used to induce human stem cells from apical papilla(SCAP)into iPSCs,respectively.The induction efficien-cies,workload of generating iPSCs,aneuploidy karyotype ratio,complexities of eliminating exogenous transcription factors and spe-cific markers expression were compared between these two systems.Results The STEMCCA reprogramming system required to prepare the feeder cell MEF.The reprogramming efficiency was 0.1%.Transcription gene-free iPSCs cells were obtained by the Cre-loxp enzyme digestion technique at the later stage.Sendai virus reprogramming system was feeder-free and the preparation of matrigel was quite simple with unified standard.The reprogramming efficiency was 0.7%,which was much higher than that of STEMCCA system(P <0.05).The exogenous virus and transgenes could be gradually eliminated after several passages of natural subclone.Conclusion The Sendai virus/matrigle reprogramming system is much more applicable for the induction of iPSCs from dental origin than the STEMCCA system.

关键词

多潜能干细胞/乳头/干细胞/慢病毒属/人诱导性多潜能干细胞/根尖乳头干细胞/重编程/仙台病毒

Key words

pluripotent stem cells/nipples/stem cells/lentivirus/human induced pluripotent stem cells/stem cells from apical papilla/reprogramming/sendai virus

分类

医药卫生

引用本文复制引用

谭小兵,徐静舒,孙贵虎,宋俊呈,戴青原..两种重编程系统诱导人牙源性多潜能干细胞的对比研究[J].重庆医学,2017,46(1):90-93,4.

基金项目

国家自然科学基金资助项目(81360161);云南省教育厅基金资助项目(2015Y153)。 ()

重庆医学

1671-8348

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