Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Rua Prof. Doutor Walter Mauricio Correa, s/n, Botucatu, São Paulo, 18618-681, Brazil.
Department of Genetic, Evolution, Microbiology and Immunology. Biology Institute, Campinas State University, Campinas, São Paulo, Brazil.
Biol Res. 2024 Oct 28;57(1):76. doi: 10.1186/s40659-024-00558-2.
There are many gaps in our understanding of the mechanisms involved in ovarian follicular development in cattle, particularly regarding follicular deviation, acquisition of ovulatory capacity, and preovulatory changes. Molecular evaluations of ovarian follicular cells during follicular development in cattle, especially serial transcriptomic analyses across key growth phases, have not been reported. This study aims to address this gap by analyzing gene expression using RNA-seq in granulosa and antral cells recovered from ovarian follicular fluid during critical phases of ovarian follicular development in Holstein cows.
Integrated analysis of gene ontology (GO), gene set enrichment (GSEA), protein-protein interaction (PPI), and gene topology identified that differentially expressed genes (DEGs) in the largest ovarian follicles at deviation (Dev) were primarily involved in FSH-negative feedback, steroidogenesis, cell proliferation, apoptosis, and the prevention of early follicle rupture. In contrast, DEGs in the second largest follicles (DevF2) were mainly related to loss of cell viability, apoptosis, and immune cell invasion. In the dominant (PostDev) and preovulatory (PreOv) follicles, DEGs were associated with vascular changes and inflammatory responses.
The transcriptome of ovarian follicular fluid cells had a predominance of granulosa cells in the dominant follicle at deviation, with upregulation of genes involved in cell viability, steroidogenesis, and apoptosis prevention, whereas in the non-selected follicle there was upregulation of cell death-related transcripts. Immune cell transcripts increased significantly after deviation, particularly in preovulatory follicles, indicating strong intrafollicular chemotactic activity. We inferred that immune cell invasion occurred despite an intact basal lamina, contributing to follicular maturation.
我们对牛卵巢卵泡发育过程中涉及的机制的理解存在许多空白,特别是在卵泡偏差、获得排卵能力和排卵前变化方面。牛卵泡发育过程中卵巢卵泡细胞的分子评估,特别是关键生长阶段的连续转录组分析,尚未报道。本研究旨在通过分析使用 RNA-seq 从荷斯坦奶牛卵巢卵泡发育关键阶段从卵巢卵泡液中回收的颗粒细胞和腔前卵泡细胞中的基因表达来填补这一空白。
基因本体论(GO)、基因集富集(GSEA)、蛋白质-蛋白质相互作用(PPI)和基因拓扑综合分析表明,在偏离时最大卵泡(Dev)中差异表达的基因(DEGs)主要参与 FSH 负反馈、类固醇生成、细胞增殖、细胞凋亡和防止早期卵泡破裂。相比之下,第二大卵泡(DevF2)中的 DEGs 主要与细胞活力丧失、细胞凋亡和免疫细胞浸润有关。在优势卵泡(PostDev)和排卵前卵泡(PreOv)中,DEGs 与血管变化和炎症反应有关。
卵巢卵泡液细胞的转录组在偏离时优势卵泡中以颗粒细胞为主,上调与细胞活力、类固醇生成和细胞凋亡预防相关的基因,而非选择卵泡中上调与细胞死亡相关的转录本。免疫细胞转录物在偏离后显著增加,特别是在排卵前卵泡中,表明强烈的卵泡内趋化活性。我们推断,尽管基底膜完整,但免疫细胞仍会浸润,从而促进卵泡成熟。