Pereira Leda Maria C, Bersano Paulo Ricardo O, Rocha Danilo D, Lopes Maria Denise
Department of Animal Reproduction and Veterinary Radiology, FMVZ- UNESP, Botucatu, São Paulo, Brazil.
Faculty of Veterinary/FAVET, State University of Ceará, Fortaleza, Ceará, Brazil.
Reprod Domest Anim. 2019 Feb;54(2):325-341. doi: 10.1111/rda.13365. Epub 2018 Nov 14.
This study aimed to investigate the localization of MPF, MAPK, p34 and cyclin B1 proteins, before and after treatment with EGF during different moments of oocyte maturation. The ovaries obtained from 350 domestic dogs were aseptically isolated, immersed in physiological solution and transported at 4°C. In the laboratory, the ovaries were sectioned for the release of cumulus-oocyte complexes. Cumulus-oocyte complexes were selected and divided into treatment groups with and without EGF and cultured for 24, 48 and 72 hr. Immunofluorescence was used for the detection and the localization of MAPK, MPF, p34 and cyclin B1 proteins. We observed that the expression and localization of MPF, MAPK, p34 and cyclin B1 proteins are associated with meiosis resumption and cell cycle progression, and that EGF influences cell signalling pathways by promoting alterations in the localization of these proteins, improving the acquisition of oocyte competence. This is the first report of the localization of crucial proteins for meiosis progression in domestic dogs and identification of the expression and localization of proteins for cell cycle progression performed in this study represented a step of great importance to elucidate the mechanisms involved in the meiosis block in domestic dogs, allowing the advance in this research area.
本研究旨在调查在卵母细胞成熟的不同阶段,经表皮生长因子(EGF)处理前后,成熟促进因子(MPF)、丝裂原活化蛋白激酶(MAPK)、p34和细胞周期蛋白B1的定位情况。从350只家犬身上无菌采集卵巢,浸入生理溶液中,并在4℃下运输。在实验室中,将卵巢切片以释放卵丘-卵母细胞复合体。挑选卵丘-卵母细胞复合体并分为添加和不添加EGF的处理组,培养24、48和72小时。采用免疫荧光法检测和定位MAPK、MPF、p34和细胞周期蛋白B1。我们观察到,MPF、MAPK、p34和细胞周期蛋白B1的表达和定位与减数分裂恢复及细胞周期进程相关,且EGF通过促进这些蛋白质定位的改变来影响细胞信号通路,从而提高卵母细胞的成熟能力。这是首次关于家犬减数分裂进程关键蛋白定位的报告,本研究中对细胞周期进程相关蛋白表达和定位的鉴定,对于阐明家犬减数分裂阻滞所涉及的机制具有重要意义,推动了该研究领域的进展。