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Donor-derived spermatogenesis following stem cell transplantation in sterile NANOS2 knockout males
Spermatogonial stem cell transplantation (SSCT) is an experimental technique for transfer of germline between donor and recipient males that could be used as a tool for biomedical research, preservation of endangered species, and dissemination of desirable genetics in food animal populations. To ful...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533891/ https://www.ncbi.nlm.nih.gov/pubmed/32929012 http://dx.doi.org/10.1073/pnas.2010102117 |
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author | Ciccarelli, Michela Giassetti, Mariana I. Miao, Deqiang Oatley, Melissa J. Robbins, Colton Lopez-Biladeau, Blanca Waqas, Muhammad Salman Tibary, Ahmed Whitelaw, Bruce Lillico, Simon Park, Chi-Hun Park, Ki-Eun Telugu, Bhanu Fan, Zhiqiang Liu, Ying Regouski, Misha Polejaeva, Irina A. Oatley, Jon M. |
author_facet | Ciccarelli, Michela Giassetti, Mariana I. Miao, Deqiang Oatley, Melissa J. Robbins, Colton Lopez-Biladeau, Blanca Waqas, Muhammad Salman Tibary, Ahmed Whitelaw, Bruce Lillico, Simon Park, Chi-Hun Park, Ki-Eun Telugu, Bhanu Fan, Zhiqiang Liu, Ying Regouski, Misha Polejaeva, Irina A. Oatley, Jon M. |
author_sort | Ciccarelli, Michela |
collection | PubMed |
description | Spermatogonial stem cell transplantation (SSCT) is an experimental technique for transfer of germline between donor and recipient males that could be used as a tool for biomedical research, preservation of endangered species, and dissemination of desirable genetics in food animal populations. To fully realize these potentials, recipient males must be devoid of endogenous germline but possess normal testicular architecture and somatic cell function capable of supporting allogeneic donor stem cell engraftment and regeneration of spermatogenesis. Here we show that male mice, pigs, goats, and cattle harboring knockout alleles of the NANOS2 gene generated by CRISPR-Cas9 editing have testes that are germline ablated but otherwise structurally normal. In adult pigs and goats, SSCT with allogeneic donor stem cells led to sustained donor-derived spermatogenesis. With prepubertal mice, allogeneic SSCT resulted in attainment of natural fertility. Collectively, these advancements represent a major step toward realizing the enormous potential of surrogate sires as a tool for dissemination and regeneration of germplasm in all mammalian species. |
format | Online Article Text |
id | pubmed-7533891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-75338912020-10-13 Donor-derived spermatogenesis following stem cell transplantation in sterile NANOS2 knockout males Ciccarelli, Michela Giassetti, Mariana I. Miao, Deqiang Oatley, Melissa J. Robbins, Colton Lopez-Biladeau, Blanca Waqas, Muhammad Salman Tibary, Ahmed Whitelaw, Bruce Lillico, Simon Park, Chi-Hun Park, Ki-Eun Telugu, Bhanu Fan, Zhiqiang Liu, Ying Regouski, Misha Polejaeva, Irina A. Oatley, Jon M. Proc Natl Acad Sci U S A Biological Sciences Spermatogonial stem cell transplantation (SSCT) is an experimental technique for transfer of germline between donor and recipient males that could be used as a tool for biomedical research, preservation of endangered species, and dissemination of desirable genetics in food animal populations. To fully realize these potentials, recipient males must be devoid of endogenous germline but possess normal testicular architecture and somatic cell function capable of supporting allogeneic donor stem cell engraftment and regeneration of spermatogenesis. Here we show that male mice, pigs, goats, and cattle harboring knockout alleles of the NANOS2 gene generated by CRISPR-Cas9 editing have testes that are germline ablated but otherwise structurally normal. In adult pigs and goats, SSCT with allogeneic donor stem cells led to sustained donor-derived spermatogenesis. With prepubertal mice, allogeneic SSCT resulted in attainment of natural fertility. Collectively, these advancements represent a major step toward realizing the enormous potential of surrogate sires as a tool for dissemination and regeneration of germplasm in all mammalian species. National Academy of Sciences 2020-09-29 2020-09-14 /pmc/articles/PMC7533891/ /pubmed/32929012 http://dx.doi.org/10.1073/pnas.2010102117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Ciccarelli, Michela Giassetti, Mariana I. Miao, Deqiang Oatley, Melissa J. Robbins, Colton Lopez-Biladeau, Blanca Waqas, Muhammad Salman Tibary, Ahmed Whitelaw, Bruce Lillico, Simon Park, Chi-Hun Park, Ki-Eun Telugu, Bhanu Fan, Zhiqiang Liu, Ying Regouski, Misha Polejaeva, Irina A. Oatley, Jon M. Donor-derived spermatogenesis following stem cell transplantation in sterile NANOS2 knockout males |
title | Donor-derived spermatogenesis following stem cell transplantation in sterile NANOS2 knockout males |
title_full | Donor-derived spermatogenesis following stem cell transplantation in sterile NANOS2 knockout males |
title_fullStr | Donor-derived spermatogenesis following stem cell transplantation in sterile NANOS2 knockout males |
title_full_unstemmed | Donor-derived spermatogenesis following stem cell transplantation in sterile NANOS2 knockout males |
title_short | Donor-derived spermatogenesis following stem cell transplantation in sterile NANOS2 knockout males |
title_sort | donor-derived spermatogenesis following stem cell transplantation in sterile nanos2 knockout males |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533891/ https://www.ncbi.nlm.nih.gov/pubmed/32929012 http://dx.doi.org/10.1073/pnas.2010102117 |
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