Abstract
Various feeder layers have been extensively applied to support the prolonged growth of human pluripotent stem cells (hPSCs) for in vitro cultures. Among them, mouse embryonic fibroblast (MEF) and mouse fibroblast cell line (SNL) are most commonly used feeder cells for hPSCs culture. However, these feeder layers from animal usually cause immunogenic contaminations, which compromises the potential of hPSCs in clinical applications. In the present study, we tested human umbilical cord mesenchymal stem cells (hUC-MSCs) as a potent xeno-free feeder system for maintaining human induced pluripotent stem cells (hiPSCs). The hUC-MSCs showed characteristics of MSCs in xeno-free culture condition. On the mitomycin-treated hUC-MSCs feeder, hiPSCs maintained the features of undifferentiated human embryonic stem cells (hESCs), such as low efficiency of spontaneous differentiation, stable expression of stemness markers, maintenance of normal karyotypes, in vitro pluripotency and in vivo ability to form teratomas, even after a prolonged culture of more than 30 passages. Our study indicates that the xeno-free culture system may be a good candidate for growth and expansion of hiPSCs as the stepping stone for stem cell research to further develop better and safer stem cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Biomarkers / metabolism
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Cell Differentiation / drug effects
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Coculture Techniques
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Embryonic Stem Cells / cytology*
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Embryonic Stem Cells / metabolism
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Feeder Cells / cytology
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Feeder Cells / drug effects
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Feeder Cells / metabolism
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Fetal Blood / cytology*
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Fetal Blood / drug effects
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Fetal Blood / metabolism
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Gene Expression
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Homeodomain Proteins / genetics
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Homeodomain Proteins / metabolism
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Humans
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Induced Pluripotent Stem Cells / cytology*
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Induced Pluripotent Stem Cells / drug effects
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Induced Pluripotent Stem Cells / metabolism
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Karyotype
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Kruppel-Like Transcription Factors / genetics
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Kruppel-Like Transcription Factors / metabolism
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Mesenchymal Stem Cells / cytology*
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Mesenchymal Stem Cells / drug effects
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Mesenchymal Stem Cells / metabolism
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Mitomycin / pharmacology
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Nanog Homeobox Protein
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Nucleic Acid Synthesis Inhibitors / pharmacology
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Octamer Transcription Factor-3 / genetics
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Octamer Transcription Factor-3 / metabolism
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Proto-Oncogene Proteins c-myc / genetics
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Proto-Oncogene Proteins c-myc / metabolism
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SOXB1 Transcription Factors / genetics
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SOXB1 Transcription Factors / metabolism
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Teratoma / pathology
Substances
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Biomarkers
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Homeodomain Proteins
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Kruppel-Like Transcription Factors
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MYC protein, human
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NANOG protein, human
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Nanog Homeobox Protein
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Nucleic Acid Synthesis Inhibitors
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Octamer Transcription Factor-3
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POU5F1 protein, human
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Proto-Oncogene Proteins c-myc
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SOX2 protein, human
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SOXB1 Transcription Factors
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ZFP42 protein, human
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Mitomycin
Grants and funding
This study was funded from the National Basic Research Program of China (973 Program); No. 2015CB964902 (website:
http://www.most.gov.cn/eng/) and the Sichuan Provincial Science and Technology Planning Project Grants; No. 2014SZ0122 (website:
http://www.scst.gov.cn/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.