Biological Activity of Cryopreserved Bovine Spermatogonial Stem Cells During In Vitro Culture

• Published in: Biology of reproduction Vol. 71; no. 3; pp. 942 - 947
• Main Authors: OATLEY, Jon M, REEVES, Jerry J, MCLEAN, Derek J
• Format: Journal Article
• Language: English
• Published: Madison, WI Society for the Study of Reproduction 01.09.2004
• Subjects: Animals; Biological and medical sciences; Cattle; Cell Culture Techniques - methods; Cell Division; Cell Survival; Cells, Cultured; Cryopreservation; Early stages. Segmentation. Gastrulation. Neurulation; Embryology: invertebrates and vertebrates. Teratology; Fibroblasts - cytology; Fundamental and applied biological sciences. Psychology; Glial Cell Line-Derived Neurotrophic Factor; Glial Cell Line-Derived Neurotrophic Factor Receptors; Male; Nerve Growth Factors - pharmacology; Proto-Oncogene Proteins - genetics; Proto-Oncogene Proteins c-ret; Receptor Protein-Tyrosine Kinases - genetics; Reverse Transcriptase Polymerase Chain Reaction; Semen Preservation; Spermatogonia - cytology; Stem Cells - cytology; Vertebrates: reproduction; Vertebrata; Reproduction; Mammalia; Cryopreservation; Stem cell; Spermatogonia; Ox; Artiodactyla; Germinal cell; In vitro; Ungulata; Biological activity
• ISSN: 0006-3363; 1529-7268
• DOI: 10.1095/biolreprod.104.028894

Functional roles of spermatogonial stem cells in spermatogenesis are self-renewing proliferation and production of differentiated daughter progeny. The ability to recapitulate these actions in vitro is important for investigating their biology and inducing genetic modification that could potentially lead to an alternative means of generating transgenic animals. The objective of this study was to evaluate the survival and proliferation of frozen-thawed bovine spermatogonial stem cells in vitro and investigate the effects of exogenous glial cell line-derived neurotrophic factor (GDNF). In order to accomplish this objective we developed a bovine embryonic fibroblast feeder cell line, termed BEF, to serve as feeder cells in a coculture system with bovine germ cells. Bovine spermatogonial stem cell survival and proliferation in vitro were evaluated by xenogeneic transplantation into the seminiferous tubules of immunodeficient mice. Bovine germ cells cocultured for 1 wk resulted in significantly more round cell donor colonies in recipient mouse testes compared to donor cells transplanted just after thawing. Bovine germ cells cocultured for 2 wk had fewer colony-forming cells than the freshly thawed cell suspensions or cells cultured for 1 wk. Characterization of the feeder cell line revealed endogenous expression of Gdnf mRNA and protein. Addition of exogenous GDNF to the culture medium decreased the number of stem cells present at 1 wk of coculture, but enhanced stem cell maintenance at 2 wk compared to cultures without added GDNF. These data indicate that frozen-thawed bovine spermatogonial stem cells survive cryopreservation and can be maintained during coculture with a feeder cell line in which the maintenance is influenced by GDNF.