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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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.
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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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