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Human-Mouse Chimerism Validates Human Stem Cell Pluripotency

Pluripotent stem cells are defined by their capacity to differentiate into all three tissue layers that comprise the body. Chimera formation, generated by stem cell transplantation to the embryo, is a stringent assessment of stem cell pluripotency. However, the ability of human pluripotent stem cell...

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Detalles Bibliográficos
Autores principales: Mascetti, Victoria L., Pedersen, Roger A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712187/
https://www.ncbi.nlm.nih.gov/pubmed/26712580
http://dx.doi.org/10.1016/j.stem.2015.11.017
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author Mascetti, Victoria L.
Pedersen, Roger A.
author_facet Mascetti, Victoria L.
Pedersen, Roger A.
author_sort Mascetti, Victoria L.
collection PubMed
description Pluripotent stem cells are defined by their capacity to differentiate into all three tissue layers that comprise the body. Chimera formation, generated by stem cell transplantation to the embryo, is a stringent assessment of stem cell pluripotency. However, the ability of human pluripotent stem cells (hPSCs) to form embryonic chimeras remains in question. Here we show using a stage-matching approach that human induced pluripotent stem cells (hiPSCs) and human embryonic stem cells (hESCs) have the capacity to participate in normal mouse development when transplanted into gastrula-stage embryos, providing in vivo functional validation of hPSC pluripotency. hiPSCs and hESCs form interspecies chimeras with high efficiency, colonize the embryo in a manner predicted from classical developmental fate mapping, and differentiate into each of the three primary tissue layers. This faithful recapitulation of tissue-specific fate post-transplantation underscores the functional potential of hPSCs and provides evidence that human-mouse interspecies developmental competency can occur.
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spelling pubmed-47121872016-02-11 Human-Mouse Chimerism Validates Human Stem Cell Pluripotency Mascetti, Victoria L. Pedersen, Roger A. Cell Stem Cell Brief Report Pluripotent stem cells are defined by their capacity to differentiate into all three tissue layers that comprise the body. Chimera formation, generated by stem cell transplantation to the embryo, is a stringent assessment of stem cell pluripotency. However, the ability of human pluripotent stem cells (hPSCs) to form embryonic chimeras remains in question. Here we show using a stage-matching approach that human induced pluripotent stem cells (hiPSCs) and human embryonic stem cells (hESCs) have the capacity to participate in normal mouse development when transplanted into gastrula-stage embryos, providing in vivo functional validation of hPSC pluripotency. hiPSCs and hESCs form interspecies chimeras with high efficiency, colonize the embryo in a manner predicted from classical developmental fate mapping, and differentiate into each of the three primary tissue layers. This faithful recapitulation of tissue-specific fate post-transplantation underscores the functional potential of hPSCs and provides evidence that human-mouse interspecies developmental competency can occur. Cell Press 2016-01-07 /pmc/articles/PMC4712187/ /pubmed/26712580 http://dx.doi.org/10.1016/j.stem.2015.11.017 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Mascetti, Victoria L.
Pedersen, Roger A.
Human-Mouse Chimerism Validates Human Stem Cell Pluripotency
title Human-Mouse Chimerism Validates Human Stem Cell Pluripotency
title_full Human-Mouse Chimerism Validates Human Stem Cell Pluripotency
title_fullStr Human-Mouse Chimerism Validates Human Stem Cell Pluripotency
title_full_unstemmed Human-Mouse Chimerism Validates Human Stem Cell Pluripotency
title_short Human-Mouse Chimerism Validates Human Stem Cell Pluripotency
title_sort human-mouse chimerism validates human stem cell pluripotency
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712187/
https://www.ncbi.nlm.nih.gov/pubmed/26712580
http://dx.doi.org/10.1016/j.stem.2015.11.017
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