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...

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Veröffentlicht in:Cells (Basel, Switzerland) Switzerland), 2023-11, Vol.12 (21), p.2582
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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 knockout (KO) causes defects in GC commitment and differentiation. We characterized -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 -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 -KO and wild-type. Intratesticular testosterone and Leydig cell volume were increased, and Leydig cell number decreased in transplanted -KO testis compared to wild-type. In summary, -KO pigs support donor-derived spermatogenesis following SSC transplantation, but low spermatogenic efficiency currently limits their use for the production of offspring.
ISSN:2073-4409
2073-4409
DOI:10.3390/cells12212582