Monitoring cell line identity in collections of human induced pluripotent stem cells

The ability to reprogram somatic cells into induced pluripotent stem cells (hiPSCs) has led to the generation of large collections of cell lines from thousands of individuals with specific phenotypes, many of which will be shared among different research groups as invaluable tools for biomedical res...

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Main Authors: Raquel Sarafian, Mariana Morato-Marques, Juliana Borsoi, Lygia Veiga Pereira
Format: Article
Language:English
Published: Elsevier 2018-04-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506118300369
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spelling doaj-68852e2932e04483a79734b2a006e9c52020-11-24T21:13:36ZengElsevierStem Cell Research1873-50612018-04-01286670Monitoring cell line identity in collections of human induced pluripotent stem cellsRaquel Sarafian0Mariana Morato-Marques1Juliana Borsoi2Lygia Veiga Pereira3National Laboratory for Embryonic Stem Cells (LaNCE), Department of Genetics and Evolutionary Biology, Biosciences Institute, University of São Paulo, SP 05508-900, BrazilNational Laboratory for Embryonic Stem Cells (LaNCE), Department of Genetics and Evolutionary Biology, Biosciences Institute, University of São Paulo, SP 05508-900, BrazilNational Laboratory for Embryonic Stem Cells (LaNCE), Department of Genetics and Evolutionary Biology, Biosciences Institute, University of São Paulo, SP 05508-900, BrazilCorresponding author.; National Laboratory for Embryonic Stem Cells (LaNCE), Department of Genetics and Evolutionary Biology, Biosciences Institute, University of São Paulo, SP 05508-900, BrazilThe ability to reprogram somatic cells into induced pluripotent stem cells (hiPSCs) has led to the generation of large collections of cell lines from thousands of individuals with specific phenotypes, many of which will be shared among different research groups as invaluable tools for biomedical research. As hiPSC-based research involves extensive culture of many cell lines, the issue periodic cell line identification is particularly important to ensure that cell line identity remains accurate. Here we analyzed the different commercially available genotyping methods considering ease of in-house genotyping, cost and informativeness, and applied one of them in our workflow for hiPSC generation. We show that the chosen STR method was able to establish a unique DNA profile for each of the 35 individuals/hiPSC lines at the examined sites, as well as identify two discrepancies resulting from inadvertently exchanged samples. Our results highlight the importance of hiPSC line genotyping by an in-house method that allows periodic cell line identification and demonstrate that STR is a useful approach to supplement less frequent karyotyping and epigenetic evaluations. Keywords: Induced pluripotent stem cells, Genotyping, Cell line identification, Short tandem repeats, Quality controlhttp://www.sciencedirect.com/science/article/pii/S1873506118300369
collection DOAJ
language English
format Article
sources DOAJ
author Raquel Sarafian
Mariana Morato-Marques
Juliana Borsoi
Lygia Veiga Pereira
spellingShingle Raquel Sarafian
Mariana Morato-Marques
Juliana Borsoi
Lygia Veiga Pereira
Monitoring cell line identity in collections of human induced pluripotent stem cells
Stem Cell Research
author_facet Raquel Sarafian
Mariana Morato-Marques
Juliana Borsoi
Lygia Veiga Pereira
author_sort Raquel Sarafian
title Monitoring cell line identity in collections of human induced pluripotent stem cells
title_short Monitoring cell line identity in collections of human induced pluripotent stem cells
title_full Monitoring cell line identity in collections of human induced pluripotent stem cells
title_fullStr Monitoring cell line identity in collections of human induced pluripotent stem cells
title_full_unstemmed Monitoring cell line identity in collections of human induced pluripotent stem cells
title_sort monitoring cell line identity in collections of human induced pluripotent stem cells
publisher Elsevier
series Stem Cell Research
issn 1873-5061
publishDate 2018-04-01
description The ability to reprogram somatic cells into induced pluripotent stem cells (hiPSCs) has led to the generation of large collections of cell lines from thousands of individuals with specific phenotypes, many of which will be shared among different research groups as invaluable tools for biomedical research. As hiPSC-based research involves extensive culture of many cell lines, the issue periodic cell line identification is particularly important to ensure that cell line identity remains accurate. Here we analyzed the different commercially available genotyping methods considering ease of in-house genotyping, cost and informativeness, and applied one of them in our workflow for hiPSC generation. We show that the chosen STR method was able to establish a unique DNA profile for each of the 35 individuals/hiPSC lines at the examined sites, as well as identify two discrepancies resulting from inadvertently exchanged samples. Our results highlight the importance of hiPSC line genotyping by an in-house method that allows periodic cell line identification and demonstrate that STR is a useful approach to supplement less frequent karyotyping and epigenetic evaluations. Keywords: Induced pluripotent stem cells, Genotyping, Cell line identification, Short tandem repeats, Quality control
url http://www.sciencedirect.com/science/article/pii/S1873506118300369
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