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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-6297357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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