Oviductal extracellular vesicles from women with endometriosis impair embryo development

ObjectiveTo investigate the influence of oviductal extracellular vesicles from patients with endometriosis on early embryo development. DesignIn vitro experimental study SettingUniversity-affiliated hospital. PatientsWomen with and without endometriosis who underwent hysterectomy (n = 27 in total). InterventionsNone. Main outcome measuresOviductal extracellular vesicles from patients with endometriosis (oEV-EMT) or without endometriosis (oEV-ctrl) were isolated and co-cultured with two-cell murine embryos for 75 hours. Blastocyst rates were recorded. RNA sequencing was used to identify the differentially expressed genes in blastocysts cultured either with oEV-EMT or with oEV-ctrl. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis were performed to identify potential biological processes in embryos that oEV-EMT affects. The functions of oEV on early embryo development were determined by reactive oxygen species (ROS) levels, mitochondrial membrane potentials (MMP), total cell numbers, and apoptotic cell proportions. ResultsExtracellular vesicles were successfully isolated from human Fallopian tubal fluid, and their characterizations were described. The blastocyst rates were significantly decreased in the oEV-EMT group. RNA sequencing revealed that oxidative phosphorylation was down-regulated in blastocysts cultured with oEV-EMT. Analysis of oxidative stress and apoptosis at the blastocysts stage showed that embryos cultured with oEV-EMT had increased ROS levels, decreased MMP, and increased apoptotic index. Total cell numbers were not influenced. ConclusionOviductal extracellular vesicles from patients with endometriosis negatively influence early embryo development by down-regulating oxidative phosphorylation.

Automated summary

This study aimed to investigate the influence of oviductal extracellular vesicles (oEV) from patients with endometriosis on early embryo development. In vitro experiments were conducted using human oEV and murine embryos. The results showed that oEV from endometriosis patients significantly decreased blastocyst rates and down-regulated oxidative phosphorylation in blastocysts. Additionally, embryos cultured with oEV from endometriosis patients exhibited increased oxidative stress and apoptosis levels. Overall, oEV from patients with endometriosis negatively affect early embryo development by interfering with oxidative phosphorylation.