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Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche

A major challenge in stem cell differentiation is the availability of bioassays to prove cell types generated in vitro are equivalent to cells in vivo. In the mouse, differentiation of primordial germ cell-like cells (PGCLCs) from pluripotent cells was validated by transplantation, leading to the ge...

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Autores principales: Sosa, Enrique, Chen, Di, Rojas, Ernesto J., Hennebold, Jon D., Peters, Karen A., Wu, Zhuang, Lam, Truong N., Mitchell, Jennifer M., Sukhwani, Meena, Tailor, Ramesh C., Meistrich, Marvin L., Orwig, Kyle E., Shetty, Gunapala, Clark, Amander T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297357/
https://www.ncbi.nlm.nih.gov/pubmed/30559363
http://dx.doi.org/10.1038/s41467-018-07740-7
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author Sosa, Enrique
Chen, Di
Rojas, Ernesto J.
Hennebold, Jon D.
Peters, Karen A.
Wu, Zhuang
Lam, Truong N.
Mitchell, Jennifer M.
Sukhwani, Meena
Tailor, Ramesh C.
Meistrich, Marvin L.
Orwig, Kyle E.
Shetty, Gunapala
Clark, Amander T.
author_facet Sosa, Enrique
Chen, Di
Rojas, Ernesto J.
Hennebold, Jon D.
Peters, Karen A.
Wu, Zhuang
Lam, Truong N.
Mitchell, Jennifer M.
Sukhwani, Meena
Tailor, Ramesh C.
Meistrich, Marvin L.
Orwig, Kyle E.
Shetty, Gunapala
Clark, Amander T.
author_sort Sosa, Enrique
collection PubMed
description A major challenge in stem cell differentiation is the availability of bioassays to prove cell types generated in vitro are equivalent to cells in vivo. In the mouse, differentiation of primordial germ cell-like cells (PGCLCs) from pluripotent cells was validated by transplantation, leading to the generation of spermatogenesis and to the birth of offspring. Here we report the use of xenotransplantation (monkey to mouse) and homologous transplantation (monkey to monkey) to validate our in vitro protocol for differentiating male rhesus (r) macaque PGCLCs (rPGCLCs) from induced pluripotent stem cells (riPSCs). Specifically, transplantation of aggregates containing rPGCLCs into mouse and nonhuman primate testicles overcomes a major bottleneck in rPGCLC differentiation. These findings suggest that immature rPGCLCs once transplanted into an adult gonadal niche commit to differentiate towards late rPGCs that initiate epigenetic reprogramming but do not complete the conversion into ENO2-positive spermatogonia.
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spelling pubmed-62973572018-12-19 Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche Sosa, Enrique Chen, Di Rojas, Ernesto J. Hennebold, Jon D. Peters, Karen A. Wu, Zhuang Lam, Truong N. Mitchell, Jennifer M. Sukhwani, Meena Tailor, Ramesh C. Meistrich, Marvin L. Orwig, Kyle E. Shetty, Gunapala Clark, Amander T. Nat Commun Article A major challenge in stem cell differentiation is the availability of bioassays to prove cell types generated in vitro are equivalent to cells in vivo. In the mouse, differentiation of primordial germ cell-like cells (PGCLCs) from pluripotent cells was validated by transplantation, leading to the generation of spermatogenesis and to the birth of offspring. Here we report the use of xenotransplantation (monkey to mouse) and homologous transplantation (monkey to monkey) to validate our in vitro protocol for differentiating male rhesus (r) macaque PGCLCs (rPGCLCs) from induced pluripotent stem cells (riPSCs). Specifically, transplantation of aggregates containing rPGCLCs into mouse and nonhuman primate testicles overcomes a major bottleneck in rPGCLC differentiation. These findings suggest that immature rPGCLCs once transplanted into an adult gonadal niche commit to differentiate towards late rPGCs that initiate epigenetic reprogramming but do not complete the conversion into ENO2-positive spermatogonia. Nature Publishing Group UK 2018-12-17 /pmc/articles/PMC6297357/ /pubmed/30559363 http://dx.doi.org/10.1038/s41467-018-07740-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sosa, Enrique
Chen, Di
Rojas, Ernesto J.
Hennebold, Jon D.
Peters, Karen A.
Wu, Zhuang
Lam, Truong N.
Mitchell, Jennifer M.
Sukhwani, Meena
Tailor, Ramesh C.
Meistrich, Marvin L.
Orwig, Kyle E.
Shetty, Gunapala
Clark, Amander T.
Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche
title Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche
title_full Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche
title_fullStr Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche
title_full_unstemmed Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche
title_short Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche
title_sort differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297357/
https://www.ncbi.nlm.nih.gov/pubmed/30559363
http://dx.doi.org/10.1038/s41467-018-07740-7
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