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DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation
Spermatogonial stem cell (SSC) transplantation into the testis of a germ cell (GC)-depleted surrogate allows transmission of donor genotype via donor-derived sperm produced by the recipient. Transplantation of gene-edited SSCs provides an approach to propagate gene-edited large animal models. DAZL i...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649044/ https://www.ncbi.nlm.nih.gov/pubmed/37947660 http://dx.doi.org/10.3390/cells12212582 |
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author | Lara, Nathalia L. M. Goldsmith, Taylor Rodriguez-Villamil, Paula Ongaratto, Felipe Solin, Staci Webster, Dennis Ganbaatar, Uyanga Hodgson, Shane Corbière, Stanislas M. A. S. Bondareva, Alla Carlson, Daniel F. Dobrinski, Ina |
author_facet | Lara, Nathalia L. M. Goldsmith, Taylor Rodriguez-Villamil, Paula Ongaratto, Felipe Solin, Staci Webster, Dennis Ganbaatar, Uyanga Hodgson, Shane Corbière, Stanislas M. A. S. Bondareva, Alla Carlson, Daniel F. Dobrinski, Ina |
author_sort | Lara, Nathalia L. M. |
collection | PubMed |
description | Spermatogonial stem cell (SSC) transplantation into the testis of a germ cell (GC)-depleted surrogate allows transmission of donor genotype via donor-derived sperm produced by the recipient. Transplantation of gene-edited SSCs provides an approach to propagate gene-edited large animal models. DAZL is a conserved RNA-binding protein important for GC development, and DAZL knockout (KO) causes defects in GC commitment and differentiation. We characterized DAZL-KO pigs as SSC transplantation recipients. While there were GCs in 1-week-old (wko) KO, complete GC depletion was observed by 10 wko. Donor GCs were transplanted into 18 DAZL-KO recipients at 10–13 wko. At sexual maturity, semen and testes were evaluated for transplantation efficiency and spermatogenesis. Approximately 22% of recipient seminiferous tubules contained GCs, including elongated spermatids and proliferating spermatogonia. The ejaculate of 89% of recipients contained sperm, exclusively from donor origin. However, sperm concentration was lower than the wild-type range. Testicular protein expression and serum hormonal levels were comparable between DAZL-KO and wild-type. Intratesticular testosterone and Leydig cell volume were increased, and Leydig cell number decreased in transplanted DAZL-KO testis compared to wild-type. In summary, DAZL-KO pigs support donor-derived spermatogenesis following SSC transplantation, but low spermatogenic efficiency currently limits their use for the production of offspring. |
format | Online Article Text |
id | pubmed-10649044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106490442023-11-06 DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation Lara, Nathalia L. M. Goldsmith, Taylor Rodriguez-Villamil, Paula Ongaratto, Felipe Solin, Staci Webster, Dennis Ganbaatar, Uyanga Hodgson, Shane Corbière, Stanislas M. A. S. Bondareva, Alla Carlson, Daniel F. Dobrinski, Ina Cells Article Spermatogonial stem cell (SSC) transplantation into the testis of a germ cell (GC)-depleted surrogate allows transmission of donor genotype via donor-derived sperm produced by the recipient. Transplantation of gene-edited SSCs provides an approach to propagate gene-edited large animal models. DAZL is a conserved RNA-binding protein important for GC development, and DAZL knockout (KO) causes defects in GC commitment and differentiation. We characterized DAZL-KO pigs as SSC transplantation recipients. While there were GCs in 1-week-old (wko) KO, complete GC depletion was observed by 10 wko. Donor GCs were transplanted into 18 DAZL-KO recipients at 10–13 wko. At sexual maturity, semen and testes were evaluated for transplantation efficiency and spermatogenesis. Approximately 22% of recipient seminiferous tubules contained GCs, including elongated spermatids and proliferating spermatogonia. The ejaculate of 89% of recipients contained sperm, exclusively from donor origin. However, sperm concentration was lower than the wild-type range. Testicular protein expression and serum hormonal levels were comparable between DAZL-KO and wild-type. Intratesticular testosterone and Leydig cell volume were increased, and Leydig cell number decreased in transplanted DAZL-KO testis compared to wild-type. In summary, DAZL-KO pigs support donor-derived spermatogenesis following SSC transplantation, but low spermatogenic efficiency currently limits their use for the production of offspring. MDPI 2023-11-06 /pmc/articles/PMC10649044/ /pubmed/37947660 http://dx.doi.org/10.3390/cells12212582 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lara, Nathalia L. M. Goldsmith, Taylor Rodriguez-Villamil, Paula Ongaratto, Felipe Solin, Staci Webster, Dennis Ganbaatar, Uyanga Hodgson, Shane Corbière, Stanislas M. A. S. Bondareva, Alla Carlson, Daniel F. Dobrinski, Ina DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation |
title | DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation |
title_full | DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation |
title_fullStr | DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation |
title_full_unstemmed | DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation |
title_short | DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation |
title_sort | dazl knockout pigs as recipients for spermatogonial stem cell transplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649044/ https://www.ncbi.nlm.nih.gov/pubmed/37947660 http://dx.doi.org/10.3390/cells12212582 |
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