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Rapid and Efficient Generation of Transgene-Free iPSC from a Small Volume of Cryopreserved Blood

Human peripheral blood and umbilical cord blood represent attractive sources of cells for reprogramming to induced pluripotent stem cells (iPSCs). However, to date, most of the blood-derived iPSCs were generated using either integrating methods or starting from T-lymphocytes that have genomic rearra...

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Autores principales: Zhou, Hongyan, Martinez, Hector, Sun, Bruce, Li, Aiqun, Zimmer, Matthew, Katsanis, Nicholas, Davis, Erica E., Kurtzberg, Joanne, Lipnick, Scott, Noggle, Scott, Rao, Mahendra, Chang, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493720/
https://www.ncbi.nlm.nih.gov/pubmed/25951995
http://dx.doi.org/10.1007/s12015-015-9586-8
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author Zhou, Hongyan
Martinez, Hector
Sun, Bruce
Li, Aiqun
Zimmer, Matthew
Katsanis, Nicholas
Davis, Erica E.
Kurtzberg, Joanne
Lipnick, Scott
Noggle, Scott
Rao, Mahendra
Chang, Stephen
author_facet Zhou, Hongyan
Martinez, Hector
Sun, Bruce
Li, Aiqun
Zimmer, Matthew
Katsanis, Nicholas
Davis, Erica E.
Kurtzberg, Joanne
Lipnick, Scott
Noggle, Scott
Rao, Mahendra
Chang, Stephen
author_sort Zhou, Hongyan
collection PubMed
description Human peripheral blood and umbilical cord blood represent attractive sources of cells for reprogramming to induced pluripotent stem cells (iPSCs). However, to date, most of the blood-derived iPSCs were generated using either integrating methods or starting from T-lymphocytes that have genomic rearrangements thus bearing uncertain consequences when using iPSC-derived lineages for disease modeling and cell therapies. Recently, both peripheral blood and cord blood cells have been reprogrammed into transgene-free iPSC using the Sendai viral vector. Here we demonstrate that peripheral blood can be utilized for medium-throughput iPSC production without the need to maintain cell culture prior to reprogramming induction. Cell reprogramming can also be accomplished with as little as 3000 previously cryopreserved cord blood cells under feeder-free and chemically defined Xeno-free conditions that are compliant with standard Good Manufacturing Practice (GMP) regulations. The first iPSC colonies appear 2–3 weeks faster in comparison to previous reports. Notably, these peripheral blood- and cord blood-derived iPSCs are free of detectable immunoglobulin heavy chain (IGH) and T cell receptor (TCR) gene rearrangements, suggesting they did not originate from B- or T- lymphoid cells. The iPSCs are pluripotent as evaluated by the scorecard assay and in vitro multi lineage functional cell differentiation. Our data show that small volumes of cryopreserved peripheral blood or cord blood cells can be reprogrammed efficiently at a convenient, cost effective and scalable way. In summary, our method expands the reprogramming potential of limited or archived samples either stored at blood banks or obtained from pediatric populations that cannot easily provide large quantities of peripheral blood or a skin biopsy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12015-015-9586-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-44937202015-07-08 Rapid and Efficient Generation of Transgene-Free iPSC from a Small Volume of Cryopreserved Blood Zhou, Hongyan Martinez, Hector Sun, Bruce Li, Aiqun Zimmer, Matthew Katsanis, Nicholas Davis, Erica E. Kurtzberg, Joanne Lipnick, Scott Noggle, Scott Rao, Mahendra Chang, Stephen Stem Cell Rev Article Human peripheral blood and umbilical cord blood represent attractive sources of cells for reprogramming to induced pluripotent stem cells (iPSCs). However, to date, most of the blood-derived iPSCs were generated using either integrating methods or starting from T-lymphocytes that have genomic rearrangements thus bearing uncertain consequences when using iPSC-derived lineages for disease modeling and cell therapies. Recently, both peripheral blood and cord blood cells have been reprogrammed into transgene-free iPSC using the Sendai viral vector. Here we demonstrate that peripheral blood can be utilized for medium-throughput iPSC production without the need to maintain cell culture prior to reprogramming induction. Cell reprogramming can also be accomplished with as little as 3000 previously cryopreserved cord blood cells under feeder-free and chemically defined Xeno-free conditions that are compliant with standard Good Manufacturing Practice (GMP) regulations. The first iPSC colonies appear 2–3 weeks faster in comparison to previous reports. Notably, these peripheral blood- and cord blood-derived iPSCs are free of detectable immunoglobulin heavy chain (IGH) and T cell receptor (TCR) gene rearrangements, suggesting they did not originate from B- or T- lymphoid cells. The iPSCs are pluripotent as evaluated by the scorecard assay and in vitro multi lineage functional cell differentiation. Our data show that small volumes of cryopreserved peripheral blood or cord blood cells can be reprogrammed efficiently at a convenient, cost effective and scalable way. In summary, our method expands the reprogramming potential of limited or archived samples either stored at blood banks or obtained from pediatric populations that cannot easily provide large quantities of peripheral blood or a skin biopsy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12015-015-9586-8) contains supplementary material, which is available to authorized users. Springer US 2015-05-08 2015 /pmc/articles/PMC4493720/ /pubmed/25951995 http://dx.doi.org/10.1007/s12015-015-9586-8 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Zhou, Hongyan
Martinez, Hector
Sun, Bruce
Li, Aiqun
Zimmer, Matthew
Katsanis, Nicholas
Davis, Erica E.
Kurtzberg, Joanne
Lipnick, Scott
Noggle, Scott
Rao, Mahendra
Chang, Stephen
Rapid and Efficient Generation of Transgene-Free iPSC from a Small Volume of Cryopreserved Blood
title Rapid and Efficient Generation of Transgene-Free iPSC from a Small Volume of Cryopreserved Blood
title_full Rapid and Efficient Generation of Transgene-Free iPSC from a Small Volume of Cryopreserved Blood
title_fullStr Rapid and Efficient Generation of Transgene-Free iPSC from a Small Volume of Cryopreserved Blood
title_full_unstemmed Rapid and Efficient Generation of Transgene-Free iPSC from a Small Volume of Cryopreserved Blood
title_short Rapid and Efficient Generation of Transgene-Free iPSC from a Small Volume of Cryopreserved Blood
title_sort rapid and efficient generation of transgene-free ipsc from a small volume of cryopreserved blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493720/
https://www.ncbi.nlm.nih.gov/pubmed/25951995
http://dx.doi.org/10.1007/s12015-015-9586-8
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