Human Seminal Extracellular Vesicles Enhance Endometrial Receptivity Through Leukemia Inhibitory Factor.
Han-Shu WangYu LinRongrong ChenYu ZhuHongqiang WangShengxian LiLei YuKaishu ZhangYujie LiuTao JingFei SunPublished in: Endocrinology (2024)
Seminal extracellular vesicles (EVs) contain different subgroups that have diverse effects on sperm function. However, the effect of seminal EVs-especially their subgroups-on endometrial receptivity is largely unknown. Here, we found that seminal EVs could be divided into high-density EVs (EV-H), medium density EVs, and low-density EVs after purification using iodixanol. We demonstrated that EV-H could promote the expression and secretion of leukemia inhibitor factor (LIF) in human endometrial cells. In EV-H-treated endometrial cells, we identified 1274 differentially expressed genes (DEGs). DEGs were enriched in cell adhesion and AKT and STAT3 pathways. Therefore, we illustrated that EV-H enhanced the adhesion of human choriocarcinoma JAr cell spheroids to endometrial cells through the LIF-STAT3 pathway. Collectively, our findings indicated that seminal EV-H could regulate endometrial receptivity through the LIF pathway, which could provide novel insights into male fertility.
Keyphrases
- induced apoptosis
- endothelial cells
- endometrial cancer
- cell cycle arrest
- high density
- cell adhesion
- induced pluripotent stem cells
- signaling pathway
- acute myeloid leukemia
- pluripotent stem cells
- endoplasmic reticulum stress
- bone marrow
- poor prognosis
- stem cells
- escherichia coli
- gene expression
- staphylococcus aureus
- single cell
- transcription factor