子宫内膜异位症
免疫系统
腹膜液
细胞内
CD14型
腹膜腔
CD3型
生物
化学
CD8型
细胞生物学
免疫学
医学
病理
解剖
作者
Chunyan Deng,Lin Zhang,Hesham K. Yosef,Yi Yang,Jinxing Jiang,Li-Na Yu,Ning Li,Karin Schütze,Min Zheng,Liguo Ma,Hui Qi,Lili Ren
摘要
Abstract In endometriosis, an aberrant immune response in the peritoneal environment is evident, but the underlying mechanism remains unclear. In recent years, some emerging data support an important role for the changes in intracellular metabolic pathways of immune cells in controlling their function. In this study, we aim to investigate the phenotypic and immunometabolism profiling of peritoneal fluid cells in endometriosis patients. By flow cytometry, our results show phenotypic profiling of peritoneal fluid cells with higher percentages of CD45 + , CD3 + , CD3 + CD8 + , CD3 + CD56 +, and CD14 + CD68 + cells and the ratio of M2 to M1 macrophages but less CD14 − CD86 + dendritic cells in endometriosis when compared with control. Label‐free single‐cell Raman trapping analysis shows intracellular changes in decreased collagen, proteins and lipids levels in CD45 + immune cells in endometriosis. In the supernatant of peritoneal fluid from endometriosis patients, Raman results reveal extracellular decreased protein and carbohydrate levels but increased lipid and fatty acid levels. Especially, Raman bands indicate both intracellular and extracellular levels of cholesterol and carotenoids decrease in endometriosis patients when compared with controls. This study provides immunometabolism features of the specific microenvironment in the peritoneal cavity and identifies some biological molecules associated with immune dysfunction in endometriosis, which may offer new clues for understanding disease pathology and therapeutic targets.
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