Burow Susann, Fontaine Romain, von Krogh Kristine, Mayer Ian, Nourizadeh-Lillabadi Rasoul, Hollander-Cohen Lian, Cohen Yaron, Shpilman Michal, Levavi-Sivan Berta, Weltzien Finn-Arne
Department of Basic Sciences and Aquatic Medicine, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, 0454 Oslo, Norway.
Department of Production Animal Clinical Sciences, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, 0454 Oslo, Norway.
Gen Comp Endocrinol. 2019 Feb 1;272:93-108. doi: 10.1016/j.ygcen.2018.12.006. Epub 2018 Dec 18.
The two gonadotropins follicle-stimulating hormone (Fsh) and luteinizing hormone (Lh) are of particular importance within the hypothalamic-pituitary-gonadal (HPG) axis of vertebrates. In the current study, we demonstrate the production and validation of Japanese medaka (Oryzias latipes) recombinant (md) gonadotropins Fshβ (mdFshβ), Lhβ (mdLhβ), Fshβα (mdFshβα), and Lhβα (mdLhβα) by Pichia pastoris, the generation of specific rabbit antibodies against their respective β subunits, and their use within the development and validation of competitive enzyme-linked immunosorbent assays (ELISAs) for quantification of medaka Fsh and Lh. mdFsh and mdLh were produced as single-chain polypeptides by linking the α subunit with mdFshβ or mdLhβ mature protein coding sequences to produce a "tethered" polypeptide with the β-chain at the N-terminal and the α-chain at the C-terminal. The specificity of the antibodies raised against mdFshβ and mdLhβ was determined by immunofluorescence (IF) for Fshβ and Lhβ on medaka pituitary tissue, while comparison with fluorescence in situ hybridization (FISH) for fshb and lhb mRNA was used for validation. Competitive ELISAs were developed using antibodies against mdFshβ or mdLhβ, and the tethered proteins mdFshβα or mdLhβα for standard curves. The standard curve for the Fsh ELISA ranged from 97.6 pg/ml to 50 ng/ml, and for the Lh ELISA from 12.21 pg/ml to 6.25 ng/ml. The sensitivity of the assays for Fsh and Lh was 44.7 and 70.8 pg/ml, respectively. A profile of pituitary protein levels of medaka Fsh and Lh comparing juveniles with adults showed significant increase of protein amount from juvenile group (body length from 12 mm to 16.5 mm) to adult group (body length from 21 mm to 26.5 mm) for both hormones in male medaka. Comparing these data to a developmental profile of pituitary mRNA expression of medaka fshb and lhb, the mRNA expression of lhb also increased during male maturation and a linear regression analysis revealed a significant increase of lhb expression with increased body length that proposes a linear model. However, fshb mRNA expression did not change significantly during male development and therefore was not correlated with body length. In summary, we have developed and validated homologous ELISA assays for medaka Fsh and Lh based on proteins produced in P. pastoris, assays that will be used to study the functions and regulations of Fsh and Lh in more detail.
两种促性腺激素,即促卵泡激素(Fsh)和促黄体生成素(Lh),在脊椎动物的下丘脑 - 垂体 - 性腺(HPG)轴中尤为重要。在本研究中,我们展示了通过毕赤酵母生产并验证日本青鳉(Oryzias latipes)重组(md)促性腺激素Fshβ(mdFshβ)、Lhβ(mdLhβ)、Fshβα(mdFshβα)和Lhβα(mdLhβα)的过程,生成了针对其各自β亚基的特异性兔抗体,并将其用于开发和验证用于定量青鳉Fsh和Lh的竞争性酶联免疫吸附测定(ELISA)。mdFsh和mdLh通过将α亚基与mdFshβ或mdLhβ成熟蛋白编码序列连接,作为单链多肽产生,从而产生一种“拴系”多肽,其β链位于N端,α链位于C端。通过对青鳉垂体组织上的Fshβ和Lhβ进行免疫荧光(IF)测定,确定针对mdFshβ和mdLhβ产生的抗体的特异性,同时与fshb和lhb mRNA的荧光原位杂交(FISH)进行比较以进行验证。使用针对mdFshβ或mdLhβ的抗体以及拴系蛋白mdFshβα或mdLhβα制作标准曲线,开发了竞争性ELISA。Fsh ELISA的标准曲线范围为97.6 pg/ml至50 ng/ml,Lh ELISA的标准曲线范围为12.21 pg/ml至6.25 ng/ml。Fsh和Lh测定的灵敏度分别为44.7和70.8 pg/ml。比较幼年和成年青鳉垂体蛋白水平的结果显示,雄性青鳉中,这两种激素从幼年组(体长12 mm至16.5 mm)到成年组(体长21 mm至26.5 mm)的蛋白量均显著增加。将这些数据与青鳉fshb和lhb垂体mRNA表达的发育图谱进行比较,lhb的mRNA表达在雄性成熟过程中也增加,线性回归分析显示lhb表达随体长增加而显著增加,提出了一个线性模型。然而,fshb mRNA表达在雄性发育过程中没有显著变化,因此与体长无关。总之,我们基于毕赤酵母中产生的蛋白质,开发并验证了用于青鳉Fsh和Lh的同源ELISA测定,这些测定将用于更详细地研究Fsh和Lh的功能和调节。