DAZL Knockout Pigs as Recipients for Spermatogonial Stem Cell Transplantation.
Nathalia L M LaraTaylor GoldsmithPaula Rodriguez-VillamilFelipe OngarattoStaci SolinDennis WebsterUyanga GanbaatarShane HodgsonStanislas M A S CorbièreAlla BondarevaDaniel F CarlsonIna DobrinskiPublished in: Cells (2023)
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.
Keyphrases
- wild type
- cell therapy
- germ cell
- stem cell transplantation
- stem cells
- high dose
- crispr cas
- binding protein
- kidney transplantation
- gas chromatography
- genome wide
- skeletal muscle
- randomized controlled trial
- mental health
- copy number
- transcription factor
- metabolic syndrome
- high resolution
- clinical trial
- mesenchymal stem cells
- genome wide identification
- bone marrow
- mass spectrometry
- polycystic ovary syndrome
- tandem mass spectrometry
- insulin resistance
- cell fate
- genome wide analysis