Journal
JOURNAL OF REPRODUCTIVE IMMUNOLOGY
Volume 148, Issue -, Pages -Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.jri.2021.103371
Keywords
Endometriosis; Polymorphonuclear myeloid-derived suppressor cells (PMN-MDSC); Low density lipoprotein receptor-1 (LOX1); Arginine 1 (Arg1); Matrix metalloproteinase 9 (MMP9)
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Funding
- Japan Agency for Medical Research and Development [JP20gk0210017h0003]
- JSPS KAKENHI [JP18K09221]
- Society of Women's Health Science Research
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The proportion of PMN-MDSCs is higher in endometriosis patients compared to controls, both in the peripheral blood and peritoneal fluid. PMN-MDSCs were detected in the stromal cell layer of endometriotic cyst wall. PMN-MDSCs may contribute to the pathogenesis of endometriosis through expression of Arg1 and MMP9.
Objectives: This study aimed to determine the systemic and local proportions, focal localization, and characteristics of polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) in endometriosis. Study design: Peripheral blood and peritoneal fluid were obtained from patients with a benign gynecologic condition (controls) or endometriosis. PMN-MDSCs were defined as CD33(+) HLA-DR(low/-)CD14(-)CD15(+) and monocytic (M)-MDSCs were defined as CD33(+)FILA-DRlow/- CD14(+)CD15(-), and were identified using flowcytometry. Ovarian endometriotic tissues were obtained, and the expression of lectin-type oxidized low density lipoprotein receptor-1 (LOX1) as a marker of PMN-MDSCs, arginine 1 (Arg1), and matrix metalloproteinase 9 (MMP9) were detected using immunohistochemistry. Anti-Ly6G antibody was administered to endometriosis model mice, and the number and weight of the lesions were measured, and cell proliferations and apoptosis in the lesions were analyzed using Ki67 immunohistochemistry and TUNEL assay. Results: In the peripheral blood, the proportion of PMN-MDSCs was significantly higher in endometriosis (3.20 vs 1.63 %, p < 0.05), but the proportion of M-MDSCs did not differ between the groups. In the peritoneal fluid, the proportion of PMN-MDSCs was significantly higher in endometriosis (7.82 x 10(-1) % vs 6.48 x 10(-2) %, p < 0.05), whereas the proportion of M-MDSCs did not differ between the groups. PMN-MDSCs were detected in the stromal cell layer of the endometriotic cyst wall. Double staining for LOX1 and Arg1, and LOX1 and MMP9 was confirmed. Administration of Ly6G antibody did not change the number or weight of endometriosis lesions, but significantly decreased Ki67-positive cells and increased TUNEL-positive cells in the lesions. Conclusions: PMN-MDSCs may contribute to the pathogenesis of endometriosis via Arg1 and MMP9 expression.
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