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Exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells
Blastocyst complementation denotes a technique that aims to generate organs, tissues, or cell types in animal chimeras via injection of pluripotent stem cells (PSCs) into genetically compromised blastocyst-stage embryos. Here, we report on successful complementation of the male germline in adult chi...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481912/ https://www.ncbi.nlm.nih.gov/pubmed/35931077 http://dx.doi.org/10.1016/j.stemcr.2022.07.005 |
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author | Zvick, Joel Tarnowska-Sengül, Monika Ghosh, Adhideb Bundschuh, Nicola Gjonlleshaj, Pjeter Hinte, Laura C. Trautmann, Christine L. Noé, Falko Qabrati, Xhem Domenig, Seraina A. Kim, Inseon Hennek, Thomas von Meyenn, Ferdinand Bar-Nur, Ori |
author_facet | Zvick, Joel Tarnowska-Sengül, Monika Ghosh, Adhideb Bundschuh, Nicola Gjonlleshaj, Pjeter Hinte, Laura C. Trautmann, Christine L. Noé, Falko Qabrati, Xhem Domenig, Seraina A. Kim, Inseon Hennek, Thomas von Meyenn, Ferdinand Bar-Nur, Ori |
author_sort | Zvick, Joel |
collection | PubMed |
description | Blastocyst complementation denotes a technique that aims to generate organs, tissues, or cell types in animal chimeras via injection of pluripotent stem cells (PSCs) into genetically compromised blastocyst-stage embryos. Here, we report on successful complementation of the male germline in adult chimeras following injection of mouse or rat PSCs into mouse blastocysts carrying a mutation in Tsc22d3, an essential gene for spermatozoa production. Injection of mouse PSCs into Tsc22d3-Knockout (KO) blastocysts gave rise to intraspecies chimeras exclusively embodying PSC-derived functional spermatozoa. In addition, injection of rat embryonic stem cells (rESCs) into Tsc22d3-KO embryos produced interspecies mouse-rat chimeras solely harboring rat spermatids and spermatozoa capable of fertilizing oocytes. Furthermore, using single-cell RNA sequencing, we deconstructed rat spermatogenesis occurring in a mouse-rat chimera testis. Collectively, this study details a method for exclusive xenogeneic germ cell production in vivo, with implications that may extend to rat transgenesis, or endangered animal species conservation efforts. |
format | Online Article Text |
id | pubmed-9481912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94819122022-09-18 Exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells Zvick, Joel Tarnowska-Sengül, Monika Ghosh, Adhideb Bundschuh, Nicola Gjonlleshaj, Pjeter Hinte, Laura C. Trautmann, Christine L. Noé, Falko Qabrati, Xhem Domenig, Seraina A. Kim, Inseon Hennek, Thomas von Meyenn, Ferdinand Bar-Nur, Ori Stem Cell Reports Article Blastocyst complementation denotes a technique that aims to generate organs, tissues, or cell types in animal chimeras via injection of pluripotent stem cells (PSCs) into genetically compromised blastocyst-stage embryos. Here, we report on successful complementation of the male germline in adult chimeras following injection of mouse or rat PSCs into mouse blastocysts carrying a mutation in Tsc22d3, an essential gene for spermatozoa production. Injection of mouse PSCs into Tsc22d3-Knockout (KO) blastocysts gave rise to intraspecies chimeras exclusively embodying PSC-derived functional spermatozoa. In addition, injection of rat embryonic stem cells (rESCs) into Tsc22d3-KO embryos produced interspecies mouse-rat chimeras solely harboring rat spermatids and spermatozoa capable of fertilizing oocytes. Furthermore, using single-cell RNA sequencing, we deconstructed rat spermatogenesis occurring in a mouse-rat chimera testis. Collectively, this study details a method for exclusive xenogeneic germ cell production in vivo, with implications that may extend to rat transgenesis, or endangered animal species conservation efforts. Elsevier 2022-08-04 /pmc/articles/PMC9481912/ /pubmed/35931077 http://dx.doi.org/10.1016/j.stemcr.2022.07.005 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Zvick, Joel Tarnowska-Sengül, Monika Ghosh, Adhideb Bundschuh, Nicola Gjonlleshaj, Pjeter Hinte, Laura C. Trautmann, Christine L. Noé, Falko Qabrati, Xhem Domenig, Seraina A. Kim, Inseon Hennek, Thomas von Meyenn, Ferdinand Bar-Nur, Ori Exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells |
title | Exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells |
title_full | Exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells |
title_fullStr | Exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells |
title_full_unstemmed | Exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells |
title_short | Exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells |
title_sort | exclusive generation of rat spermatozoa in sterile mice utilizing blastocyst complementation with pluripotent stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481912/ https://www.ncbi.nlm.nih.gov/pubmed/35931077 http://dx.doi.org/10.1016/j.stemcr.2022.07.005 |
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