Department of Physiological Sciences, Institute of Biological Sciences, University of Brasília, Brasília, Brazil.
School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.
Reprod Domest Anim. 2022 Jan;57(1):19-32. doi: 10.1111/rda.14025. Epub 2021 Oct 17.
The molecular mechanisms regulating follicular development and ensuring primordial follicle activation remain undefined. To help elucidate these mechanisms, this proteomic study of bovine ovarian tissue identified the differential molecular profiles of preantral follicles together with the spatial distribution of the most abundant molecular components in the tissue. Isolated primordial, primary and secondary follicles were individually placed on a MALDI target plate for mass spectral acquisitions, with detection of different m/z ranges. Ovarian tissue was sectioned and analysed in the m/z 400-2,000 range. Results of the first analysis indicated a similarity pattern in the molecular protein profile among different follicular classes in the m/z ranges of 100-1000 and 25,000-200,000, but in the m/z ranges of 800-4000, 4000-20,000 and 15,000-70,000, primary and secondary follicles shared similar clustering profiles which were different from primordial follicles (p < .05). In the second analysis, it was possible to correlate some intense molecular components in the tissue from global mass spectrum with the ions detected in the first analysis. Molecular components at m/z 11,325 (±230) were also detected in primary and secondary follicles in the experiment with isolated follicles, in addition to ions at m/z 4,029 (±120), 13,799 (±70), 5,547 (±9), 15,313 (±200), 7,018 (±40) and 7,663 (±90) which were also intensely detected in primary and secondary follicles. The present proteomic approaches evaluated different mass ranges of preantral follicles in bovine ovarian tissue and also indicated the spatial distribution of the most abundant molecular components. This study hopes to pave the way for future research identifying and characterizing specific proteins involved in follicle activation in bovine follicles, in order to better understand folliculogenesis and potentially improve mammalian follicle culture systems.
调控卵泡发育和确保原始卵泡激活的分子机制尚不清楚。为了帮助阐明这些机制,本项牛卵巢组织的蛋白质组学研究鉴定了前腔卵泡的差异分子谱,以及组织中最丰富的分子成分的空间分布。将分离的原始卵泡、初级卵泡和次级卵泡分别放置在 MALDI 靶板上进行质谱采集,检测不同的 m/z 范围。对卵巢组织进行切片,并在 m/z 400-2000 范围内进行分析。第一次分析的结果表明,不同卵泡类群在 m/z 100-1000 和 25000-200000 范围内的分子蛋白谱具有相似的模式,但在 m/z 800-4000、4000-20000 和 15000-70000 范围内,初级和次级卵泡具有相似的聚类谱,与原始卵泡不同(p<.05)。在第二次分析中,有可能将组织中一些强烈的分子成分与第一次分析中检测到的离子相关联。在分离卵泡的实验中,除了在 m/z 4029(±120)、13799(±70)、5547(±9)、15313(±200)、7018(±40)和 7663(±90)处检测到的离子外,还检测到 m/z 11325(±230)处的分子成分,这些离子也在初级和次级卵泡中强烈检测到。本蛋白质组学方法评估了牛卵巢组织中前腔卵泡的不同质量范围,并指出了最丰富的分子成分的空间分布。本研究希望为未来的研究铺平道路,鉴定和表征牛卵泡中参与卵泡激活的特定蛋白质,以更好地理解卵泡发生,并有可能改善哺乳动物卵泡培养系统。