Gr1+ myeloid-derived suppressor cells participate in the regulation of lung–gut axis during mouse emphysema model. Issue 9 (30th September 2022)

• Record Type: Journal Article
• Authors: Yang, Jing; Zeng, Jiajia; Yang, Shuaini; Guan, Xin; Gao, Qiaoying; He, Simeng; Wu, Xiaoyang; Ge, Lixiu; Bai, Hong
• Is Part Of: Bioscience reports. Volume 42:Issue 9(2022)
• Publication Date: 2022-09-30
• Subjects: COPD -- Emphysema -- lung-gut axis -- macrophages -- MDSCs; Molecular biology -- Periodicals; Cytology -- Periodicals; 572.8
• DOI: 10.1042/BSR20221041
• Languages: English
• ISSNs: 0144-8463

Abstract

Abstract: Background: Chronic obstructive pulmonary disease (COPD) is often accompanied by intestinal symptoms. Myeloid-derived suppressor cells (MDSCs) possess immunosuppressive ability in cancer, chronic inflammation, and infection. The aim of this study was to verify the distribution of MDSCs in emphysema mouse model and participation in lung–gut cross-talk. Methods: Adult male C57BL/6 mice were exposed to cigarette smoke (CS) for 6 months or injected with porcine pancreas elastase to establish emphysema models. Flow cytometry and immunohistochemistry analysis revealed the distribution of MDSCs in tissues. The expression of inflammation and MDSCs-associated genes in the small intestine and colon were analyzed by real-time PCR. Results: The small intestine and colon of CS-induced emphysematous mice displayed pathological changes, CD4 + /CD8 + T cells imbalance, and increased neutrophils, monocytes, and macrophages infiltration. A significant expansion of MDSCs could be seen in CS-affected respiratory and gastrointestinal tract. Importantly, higher expression of MDSCs-related effector molecules inducible nitric oxide synthase (INOS), NADPH oxidase 2 (NOX2), and arginase 1 (ARG-1) suggested the immunosuppressive effect of migrated MDSCs ( P <0.05). Conclusion: These data provide evidence for lung–gut axis in emphysema model and the participants of MDSCs.