Xenotransplantation of European Eel (Anguilla anguilla) Spermatogonia in Zebrafish (Danio rerio) and European Sea Bass (Dicentrarchus labrax)

IF 2.1 3区 农林科学 Q2 FISHERIES
Fishes Pub Date : 2024-07-21 DOI:10.3390/fishes9070290
M. Blanes-García, Z. Marinović, M. Morini, Alain Vergnet, Á. Horváth, J. Asturiano
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Abstract

The European eel encounters challenges in achieving sexual maturation in captivity, which has been a concern for researchers. This study explores surrogate broodstock technology as an alternative approach for eel production. The present study aimed to evaluate zebrafish and European sea bass as potential recipients for European eel spermatogonia transplantation, given the abundance of eel type A spermatogonia (SPGA). Immature European eel testes were dissected and maintained at 4 °C or cryopreserved. SPGA were obtained by dissociation of fresh or post-thawed tissue, employing an enzymatic solution, and then labelled with fluorescent membrane marker PKH26. SPGA from fresh tissue were transplanted into wild-type zebrafish larvae and triploid European sea bass larvae, while SPGA from cryopreserved testis were transplanted into vasa::egfp transgenic zebrafish larvae. One-and-a-half months post-transplantation (mpt), fluorescent donor cells were not detected in the gonads of zebrafish or European sea bass. Molecular qPCR analyses at 1.5 or 6 mpt did not reveal European eel-specific gene expression in the gonads of any transplanted fish. The findings suggest that the gonadal microenvironments of zebrafish and European sea bass are unsuitable for the development of European eel spermatogonia, highlighting distinctive spermatogonial stem cell migration mechanisms within teleost species
欧洲鳗鲡精原细胞在斑马鱼(Danio rerio)和欧洲鲈鱼(Dicentrarchus labrax)中的异种移植
欧洲鳗鱼在人工饲养条件下实现性成熟面临挑战,这一直是研究人员关注的问题。本研究探讨了替代育种技术作为鳗鱼生产的替代方法。本研究旨在评估斑马鱼和欧洲鲈鱼作为欧洲鳗精原细胞移植的潜在受体的可能性,因为欧洲鳗的A型精原细胞(SPGA)非常丰富。解剖未成熟的欧洲鳗鲡睾丸并将其保存在4 °C或低温保存。用酶解法解离新鲜或解冻后的组织,然后用荧光膜标记物PKH26标记,获得SPGA。将新鲜组织中的SPGA移植到野生型斑马鱼幼体和三倍体欧洲鲈鱼幼体中,而将冷冻保存的睾丸中的SPGA移植到vasa::egfp转基因斑马鱼幼体中。移植后一个半月(mpt),在斑马鱼或欧洲鲈的性腺中均未检测到荧光供体细胞。在 1.5 个月或 6 个月时进行的分子 qPCR 分析未在任何移植鱼的性腺中发现欧洲鳗鱼特异性基因表达。研究结果表明,斑马鱼和欧洲鲈鱼的性腺微环境不适合欧洲鳗精原细胞的发育,凸显了远东鱼类中精原干细胞迁移机制的独特性。
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来源期刊
Fishes
Fishes Multiple-
CiteScore
1.90
自引率
8.70%
发文量
311
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