Institute of Bioscience, São Paulo State University, Botucatu, São Paulo, Brazil.
Laboratory of Fish Biotechnology, Chico Mendes Institute of Biodiversity Conservation/National Center for Research and Conservation of Continental Aquatic Biodiversity, Pirassununga, São Paulo, Brazil.
Fish Physiol Biochem. 2024 Oct;50(5):2117-2135. doi: 10.1007/s10695-024-01406-6. Epub 2024 Sep 27.
Piracanjuba (Brycon orbignyanus) is an endangered fish species from the Neotropical region. The establishment of a cryobank using spermatogonial stem cells (SSCs) and subsequent production of a germline chimera is thus a promising strategy for such species. In the present work, procedures for the isolation and cryopreservation of piracanjuba SSCs and subsequent transplantation into sterile recipients were established. The piracanjuba SSCs were obtained by Percoll density gradient centrifugation and differential plating. SSC fractions were evaluated by relative ddx4 expression, alkaline phosphatase activity, and light microscopy. SSC cryopreservation was performed using five cryoprotectants at three different concentrations. The mix of the cells from the 20% and 30% Percoll density gradients showed 58.35 ± 0.03% purity of SSCs. The purity of SSCs increased to 66.00 ± 0.01% after differential plating. The relative ddx4 expression was 3.5 times higher in cells from the Percoll density gradient centrifugation than in the gonad and cells after differential plating. Propanediol (1 M) was the most effective cryoprotector evaluated (P = 1.000), showing 90.75 ± 1.85% cell viability. Freshly isolated and cryopreserved cells from the Percoll density gradient centrifugation were transplanted into a sterile male adult triploid hybrid with germ cell-less gonads. SSCs were observed in the germinal epithelium of the testes of recipients 20 days after transplantation. The results are promising for obtaining functional germline chimeras in Neotropical fish. Consequently, although the number of males used for the experiment was borderline, the procedures established here can be applied in future actions for the conservation and reconstitution of the piracanjuba in case of extinction.
皮拉坎朱巴鱼(Brycon orbignyanus)是一种来自新热带地区的濒危鱼类。因此,建立使用精原干细胞(SSC)的低温库并随后产生生殖系嵌合体是一种有前途的策略。在本工作中,建立了皮拉坎朱巴鱼 SSC 的分离和冷冻保存以及随后移植到无菌受体的程序。通过 Percoll 密度梯度离心和差速贴壁分离获得 SSC fractions,通过相对 ddx4 表达、碱性磷酸酶活性和相差显微镜评估 SSC fractions。使用五种不同浓度的冷冻保护剂对 SSC 进行冷冻保存。20%和 30%Percoll 密度梯度的细胞混合物显示 SSCs 的纯度为 58.35±0.03%。经过差速贴壁培养后,SSCs 的纯度增加到 66.00±0.01%。与性腺和差速贴壁培养后的细胞相比,Percoll 密度梯度离心后的细胞中的相对 ddx4 表达增加了 3.5 倍。在所评估的冷冻保护剂中,丙二醇(1 M)是最有效的(P=1.000),细胞活力为 90.75±1.85%。从 Percoll 密度梯度离心中分离和冷冻保存的新鲜细胞被移植到没有生殖细胞的性腺的无菌成年三倍体杂种中。移植后 20 天,在受体的睾丸生殖上皮中观察到 SSCs。这些结果为在新热带鱼类中获得功能性生殖系嵌合体提供了希望。因此,尽管用于实验的雄性数量接近边缘,但此处建立的程序可应用于未来的行动,以在灭绝的情况下保护和重建皮拉坎朱巴鱼。