Nabulindo Nakami Wilkister, Nguhiu-Mwangi James, Kipyegon Ambrose Ng'eno, Ogugo Moses, Muteti Charity, Christian Tiambo, Oatley Melissa J, Oatley Jon M, Kemp Stephen
Centre for Tropical Livestock Genetics and Health Laboratory, International Livestock Research Institute, Nairobi, Kenya.
Department of Clinical Studies, Faculty of Veterinary Medicine, University of Nairobi, Nairobi, Kenya.
Front Vet Sci. 2022 Jul 19;9:894075. doi: 10.3389/fvets.2022.894075. eCollection 2022.
The undifferentiated spermatogonial population in mammalian testes contains a spermatogonial stem cell (SSC) population that can regenerate continual spermatogenesis following transplantation. This capacity has the potential to be exploited as a surrogate sires breeding tool to achieve widespread dissemination of desirable genetics in livestock production. Because SSCs are relatively rare in testicular tissue, the ability to expand a population would be advantageous to provide large numbers for transplantation into surrogate recipient males. Here, we evaluated conditions that would support long-term maintenance of undifferentiated spermatogonia from a goat breed that is endemic to Kenyan livestock production. Single-cell suspensions enriched for undifferentiated spermatogonia from pre-pubertal bucks were seeded on laminin-coated tissue culture plates and maintained in a commercial media based on serum-free composition. The serum-free media was conditioned on goat fetal fibroblasts and supplemented with a growth factor cocktail that included glial cell line-derived neurotrophic factor (GDNF), leukemia inhibitory factor (LIF), stromal cell-derived factor (SDF), and fibroblast growth factor (FGF) before use. Over 45 days, the primary cultures developed a cluster morphology indicative of grown undifferentiated spermatogonia from other species and expressed the germ cell marker VASA, as well as the previously defined spermatogonial marker such as promyelocytic leukemia zinc finger (PLZF). Taken together, these findings provide a methodology for isolating the SSC containing undifferentiated spermatogonial population from goat testes and long-term maintenance in defined culture conditions.
哺乳动物睾丸中的未分化精原细胞群体包含精原干细胞(SSC)群体,该群体在移植后能够再生持续的精子发生。这种能力有潜力被用作替代种畜繁殖工具,以在畜牧生产中广泛传播优良基因。由于精原干细胞在睾丸组织中相对稀少,扩大其群体数量的能力将有利于提供大量细胞用于移植到替代受体雄性动物体内。在此,我们评估了支持肯尼亚畜牧生产特有的一个山羊品种未分化精原细胞长期维持的条件。将从青春期前雄羊中富集的未分化精原细胞单细胞悬液接种在层粘连蛋白包被的组织培养板上,并在基于无血清成分的商业培养基中培养。该无血清培养基用山羊胎儿成纤维细胞进行预处理,并在使用前补充生长因子混合物,其中包括胶质细胞系衍生的神经营养因子(GDNF)、白血病抑制因子(LIF)、基质细胞衍生因子(SDF)和成纤维细胞生长因子(FGF)。在45天的时间里,原代培养物形成了一种簇状形态,这表明从未分化的精原细胞生长而来,与其他物种的情况相似,并且表达了生殖细胞标志物VASA以及先前定义的精原细胞标志物,如早幼粒细胞白血病锌指蛋白(PLZF)。综上所述,这些发现提供了一种从山羊睾丸中分离包含精原干细胞的未分化精原细胞群体并在特定培养条件下进行长期维持的方法。