Grupo de Acuicultura y Biodiversidad, Instituto de Ciencia y Tecnología Animal, Universitat Politècnica de València, Camino de Vera S/N, 46022, Valencia, Spain.
Department of Aquaculture, Institute of Aquaculture and Environmental Safety, Hungarian University of Agriculture and Life Sciences, Páter Károly U. 1, 2100, Gödöllő, Hungary.
Fish Physiol Biochem. 2024 Oct;50(5):2099-2115. doi: 10.1007/s10695-024-01338-1. Epub 2024 Apr 19.
Identification of specific molecular markers for spermatogonial stem cells in teleost is crucial for enhancing the efficacy of reproductive biotechnologies in aquaculture, such as transplantation and surrogate production in fishes. Since it is not yet possible to distinguish spermatogonial stem cells of European eel (Anguilla anguilla) using specific molecular markers, we isolated spermatogonial cells from immature European eels to find these potential markers. We attempted this by studying three candidate genes: vasa, nanos2, and dnd1. Two vasa (vasa1 and vasa2) genes, nanos2, and dnd1 were identified, characterized, and studied in the muscle, testis, and isolated spermatogonia. Our results showed that vasa1 and vasa2 had the highest levels of expression when measured by qPCR. In situ hybridization and immunochemistry assays showed that the four genes were localized explicitly in type A spermatogonia. However, vasa1 and vasa2 exhibited stronger signals in the immature testicular tissue than the other two potential markers. According to this, vasa1 and vasa2 were found to be the most effective markers for spermatogonial cells in the European eel.
鉴定鱼类精原干细胞的特定分子标记对于提高水产养殖中生殖生物技术的效率至关重要,如鱼类的移植和代孕生产。由于目前还无法使用特定的分子标记来区分欧鳗(Anguilla anguilla)的精原干细胞,我们从未成熟的欧鳗中分离出精原细胞,以寻找这些潜在的标记物。我们通过研究三个候选基因:vasa、nanos2 和 dnd1 来尝试实现这一目标。我们鉴定、表征了两个 vasa(vasa1 和 vasa2)基因、nanos2 和 dnd1,并在肌肉、睾丸和分离的精原细胞中进行了研究。我们的结果表明,qPCR 测量显示 vasa1 和 vasa2 的表达水平最高。原位杂交和免疫组织化学检测表明,这四个基因在 A 型精原细胞中特异性定位。然而,vasa1 和 vasa2 在未成熟的睾丸组织中的信号比其他两个潜在标记物更强。因此,vasa1 和 vasa2 被发现是欧鳗精原细胞最有效的标记物。