Reproductive Medicine Centre, The Affiliated Taizhou People's Hospital of Nanjing Medical University, Taizhou, China.
Graduate School, Nanjing Medical University, Nanjing, China.
Reprod Biol Endocrinol. 2024 Aug 20;22(1):105. doi: 10.1186/s12958-024-01279-7.
Obesity is a global health issue with detrimental effects on various human organs, including the reproductive system. Observational human data and several lines of animal experimental data suggest that maternal obesity impairs ovarian function and early embryo development, but the precise pathogenesis remains unclear.
We established a high-fat diet (HFD)-induced obese female mouse model to assess systemic metabolism, ovarian morphology, and oocyte function in mice. For the first time, this study employed single-cell RNA sequencing to explore the altered transcriptomic landscape of preimplantation embryos at different stages in HFD-induced obese mice. Differential gene expression analysis, enrichment analysis and protein-protein interactions network analysis were performed.
HFD-induced obese female mice exhibited impaired glucolipid metabolism and insulin resistance. The ovaries of HFD mice had a reduced total follicle number, an increased proportion of atretic follicles, and irregular granulosa cell arrangement. Furthermore, the maturation rate of embryonic development by in vitro fertilization of oocytes was significantly decreased in HFD mice. Additionally, the transcriptional landscapes of preimplantation embryos at different stages in mice induced by different diets were significantly distinguished. The maternal-to-zygotic transition was also affected by the failure to remove maternal RNAs and to turn off zygotic genome expression.
HFD-induced obesity impaired ovarian morphology and oocyte function in female mice and further led to alterations in the transcriptional landscape of preimplantation embryos at different stages of HFD mice.
肥胖是一个全球性的健康问题,对包括生殖系统在内的各种人体器官都有不利影响。观察性人体数据和几条动物实验数据表明,母体肥胖会损害卵巢功能和早期胚胎发育,但确切的发病机制尚不清楚。
我们建立了高脂肪饮食(HFD)诱导的肥胖雌性小鼠模型,以评估肥胖对小鼠全身代谢、卵巢形态和卵母细胞功能的影响。本研究首次采用单细胞 RNA 测序技术,探讨 HFD 诱导肥胖小鼠不同阶段着床前胚胎转录组的改变。进行差异基因表达分析、富集分析和蛋白质-蛋白质相互作用网络分析。
HFD 诱导的肥胖雌性小鼠表现出糖脂代谢受损和胰岛素抵抗。HFD 组小鼠的卵巢总卵泡数减少,闭锁卵泡比例增加,颗粒细胞排列不规则。此外,HFD 组小鼠卵母细胞体外受精的胚胎发育成熟率显著降低。此外,不同饮食诱导的小鼠着床前胚胎在不同阶段的转录组图谱也有明显区别。母源到合子的转变也受到未能去除母源 RNA 和关闭合子基因组表达的影响。
HFD 诱导的肥胖会损害雌性小鼠的卵巢形态和卵母细胞功能,并进一步导致 HFD 小鼠不同阶段着床前胚胎转录组的改变。