Department of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad, Iran; Department of Reproductive Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Theriogenology. 2013 Nov;80(8):923-32. doi: 10.1016/j.theriogenology.2013.07.020. Epub 2013 Aug 27.
Spermatogonial stem cells are unique cells of testes that can restore fertility upon transplantation into recipient testes. However, use of suitable markers for enrichment of these cells have important potential application. THY1, is an established conserved marker of spermatogonial stem cells in bovine, rodents, and primates, but there is no information available in goats. After three rounds of enzymatic digestion of prepubertal goat testicular tissues, undifferentiated spermatogonia positive for THY1 were isolated by magnetic-activated cell sorting and were used for immunocytochemistry, real-time polymerase chain reaction analysis for gene expression, protein expression, and transplantation into recipient mice. Immunocytochemical analyses showed that significantly higher percentage of THY1(+) cells were positive for PLZF and VASA when compared with unselected population. This result for PLZF was further confirmed at the protein level. Real-time polymerase chain reaction analysis revealed that expression of THY1, PLZF, VASA, BCL6B, and UCHL1 as SCCs characteristic genes in THY1(+) cells was significantly higher than in the initial population. Finally, transplantation of PKH26-labeled cells revealed that THY1(+) cells had higher capacity for colony formation when compared with unselected cells. In conclusion, the results provide indications that THY1 surface marker can be reliably used for enrichment of undifferentiated spermatogonial in the goats.
精原干细胞是睾丸中具有独特功能的细胞,它们可以在移植到受体睾丸后恢复生育能力。然而,使用合适的标记物来富集这些细胞具有重要的潜在应用价值。THY1 是牛、啮齿动物和灵长类动物精原干细胞的一种已确立的保守标记物,但在山羊中尚无相关信息。在对未成年山羊睾丸组织进行三轮酶消化后,通过磁激活细胞分选分离出 THY1 阳性的未分化精原细胞,并用于免疫细胞化学、实时聚合酶链反应分析基因表达、蛋白质表达和移植到受体小鼠中。免疫细胞化学分析表明,与未分选的群体相比,THY1(+)细胞中显著更高比例的细胞对 PLZF 和 VASA 呈阳性。PLZF 的这一结果在蛋白质水平上得到了进一步证实。实时聚合酶链反应分析显示,THY1、PLZF、VASA、BCL6B 和 UCHL1 作为 SCC 特征基因在 THY1(+)细胞中的表达明显高于初始群体。最后,PKH26 标记细胞的移植表明,与未分选的细胞相比,THY1(+)细胞具有更高的集落形成能力。总之,这些结果表明,THY1 表面标记物可用于山羊未分化精原细胞的富集。