Key Laboratory of Animal Genetics, Breeding and Reproduction in the Plateau Mountainous Region, Ministry of Education, Guizhou University, Guiyang 550025, China.
Key Laboratory of Animal Genetics, Breeding and Reproduction, Guiyang 550025, China.
Genes (Basel). 2022 Dec 7;13(12):2306. doi: 10.3390/genes13122306.
The purpose of this paper was to investigate the effects of N-acetylcysteine (NAC) on the proliferation, hormone secretion, and mRNA expression profiles of ovarian granulosa cells (GCs) in vitro. A total of 12 ovaries from 6 follicular-stage goats were collected for granulosa cell extraction. The optimum concentration of NAC addition was determined to be 200 μM via the Cell Counting Kit 8 (CCK-8) method. Next, GCs were cultured in a medium supplemented with 200 μM NAC (200 μM NAC group) and 0 μ M NAC (control group) for 48 h. The effects of 200 μM NAC on the proliferation of granulosa cells and hormones were studied by 5-ethynyl-2'-deoxyuridine (EdU) assay and enzyme-linked immunosorbent assay (ELISA). mRNA expression was analyzed by transcriptome sequencing. The results indicate that 200 μM NAC significantly increased cell viability and the proportion of cells in the S phase but promoted hormone secretion to a lesser degree. Overall, 122 differentially expressed genes (DEGs) were identified. A total of 51 upregulated and 71 downregulated genes were included. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses indicated that the most DEGs were enriched in terms of cell growth regulation, cell growth, neuroactive ligand-receptor interaction, cytokine-cytokine receptor interaction, the cAMP-signaling pathway, and the Wnt-signaling pathway. Seven genes related to granulosa cell proliferation were screened, , , , , , , and . The above results provide molecular theoretical support for NAC as a feed additive to improve follicle development and improve reproductive performance in ewes.
本研究旨在探讨 N-乙酰半胱氨酸(NAC)对体外卵巢颗粒细胞(GCs)增殖、激素分泌和 mRNA 表达谱的影响。共采集 6 只卵泡期山羊的 12 个卵巢用于提取颗粒细胞。通过细胞计数试剂盒 8(CCK-8)法确定 NAC 的最佳添加浓度为 200 μM。接下来,将 GCs 在添加 200 μM NAC(200 μM NAC 组)和 0 μM NAC(对照组)的培养基中培养 48 h。通过 5-乙炔基-2'-脱氧尿苷(EdU)检测和酶联免疫吸附测定(ELISA)研究 200 μM NAC 对颗粒细胞增殖和激素的影响。通过转录组测序分析 mRNA 表达。结果表明,200 μM NAC 显著提高了细胞活力和 S 期细胞的比例,但对激素分泌的促进作用较小。总的来说,鉴定出 122 个差异表达基因(DEGs)。共包括 51 个上调基因和 71 个下调基因。基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析表明,大多数 DEGs 富集在细胞生长调节、细胞生长、神经活性配体-受体相互作用、细胞因子-细胞因子受体相互作用、cAMP 信号通路和 Wnt 信号通路等方面。筛选出与颗粒细胞增殖相关的 7 个基因,分别为 、 、 、 、 、 、 。上述结果为 NAC 作为饲料添加剂改善绵羊卵泡发育和提高繁殖性能提供了分子理论支持。