Department of Fish Physiology and Biotechnology, Institute of Aquaculture Torre de Sal, Spanish National Research Council (CSIC), Torre de Sal s/n, 12595 Ribera de Cabanes, Castellón, Spain.
Gen Comp Endocrinol. 2012 Mar 1;176(1):70-8. doi: 10.1016/j.ygcen.2011.12.029. Epub 2012 Jan 2.
Since the late 1980s, gonadotropins have been isolated and characterized in several fish species, but specific immunoassays for the follicle-stimulating hormone (FSH) have only been developed for a few. The present study reports the development and use of a specific and homologous competitive ELISA for measuring FSH in European sea bass (Dicentrarchus labrax) using a recombinant FSH and its specific antiserum. Recombinant European sea bass FSHβ and FSH heterodimer were produced in the methylotrophic yeast Pichia pastoris and a baculovirus expression system, respectively. Specific polyclonal antibodies, generated by rabbit immunization against recombinant FSHβ, were used at a final dilution of 1:8000. Recombinant FSH heterodimer was used to generate a standard curve and for coating of microplates (166 μg/ml). The sensitivity of the assay was 0.5 ng/ml [B(0)-2SD], and the intra- and inter-assay coefficients of variation were 2.12% (n=10) and 5.44% (n=16) (B(i)/B(0) ∼45%), respectively. A high degree of parallelism was observed between the standard curve and serially diluted plasma and pituitary samples of European sea bass. The ELISA developed was used to study the plasma FSH profiles of mature males and females during the reproductive cycle, and those of immature juvenile males under different light regimes. The analysis showed that FSH increased significantly during the intermediate stages of spermatogenesis and during vitellogenesis. Analyses in immature juvenile males showed that the continuous light photoperiod significantly reduced plasma FSH levels, and consequently, testicular growth and precocious puberty. In conclusion, the immunoassay developed has proven to be sensitive, specific and accurate for measuring European sea bass FSH, and it represents a valuable tool for future studies on the reproductive endocrinology of this species.
自 20 世纪 80 年代末以来,已经在几种鱼类中分离和鉴定了促性腺激素,但仅为少数几种鱼类开发了特定的促卵泡激素(FSH)免疫测定法。本研究报告了使用重组 FSH 及其特异性抗血清,通过欧洲鲈鱼(Dicentrarchus labrax)的卵泡刺激素(FSH)的特异性和同源竞争 ELISA 的开发和应用。重组欧洲鲈鱼 FSHβ和 FSH 异二聚体分别在甲醇营养酵母毕赤酵母和杆状病毒表达系统中产生。针对重组 FSHβ的兔免疫产生了特异性多克隆抗体,最终稀释度为 1:8000。使用重组 FSH 异二聚体生成标准曲线和包被微孔板(166μg/ml)。该测定的灵敏度为 0.5ng/ml [B(0)-2SD],批内和批间变异系数分别为 2.12%(n=10)和 5.44%(n=16)(B(i)/B(0)∼45%)。标准曲线与欧洲鲈鱼的血浆和垂体样品的系列稀释液之间观察到高度的平行性。开发的 ELISA 用于研究成熟雄性和雌性在生殖周期以及不同光照条件下未成熟幼鱼的血浆 FSH 谱。分析表明,FSH 在精子发生的中间阶段和卵黄发生期间显着增加。对未成熟幼鱼的分析表明,连续光照光周期显著降低了血浆 FSH 水平,从而减少了睾丸生长和性早熟。总之,开发的免疫测定法已被证明对测量欧洲鲈鱼 FSH 具有灵敏,特异和准确的作用,它代表了该物种生殖内分泌学未来研究的有价值的工具。