Pulmonary resident neutrophils regulate the production of GM-CSF and alveolar macrophages

被引:12
|
作者
Tian, Feng [1 ]
Han, Yong [1 ]
Song, Jian [2 ]
Lei, Jie [1 ]
Yan, Xiaolong [1 ]
Xie, Nianlin [1 ]
Wang, Jian [1 ]
Zhao, Jinbo [1 ]
Liang, Xiaohua [1 ]
Zhong, Daixing [1 ]
Zhou, Yongan [1 ]
Wang, Xiaoping [1 ]
Li, Xiaofei [1 ]
机构
[1] Fourth Mil Med Univ, Tangdu Hosp, Dept Thorac Surg, Xinsi Rd 569, Xian 710035, Shaanxi, Peoples R China
[2] Univ Cologne, Ctr Mol Med Cologne, Cologne, Germany
基金
中国国家自然科学基金;
关键词
alveolar macrophages; CD18; GM-CSF; IL-23; neutrophils; COLONY-STIMULATING FACTOR; INNATE LYMPHOID-CELLS; FETAL MONOCYTES; GRANULOPOIESIS; PHAGOCYTOSIS; HOMEOSTASIS; FIBROSIS; IL-23; GAMMA; LUNG;
D O I
10.1111/febs.13684
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alveolar macrophages exist in the lung airspaces, and their differentiation and function are considerably regulated by the microenvironment. In this study, we examine the important role of resident neutrophil/IL-23/granulocyte/macrophage colony-stimulating factor (GM-CSF) axis in the development and preferential phenotype of alveolar macrophages under physiological conditions. Using CD18-deficient (CD18(-/-)) mice, we show a correlation between increased granulopoiesis and enhanced alveolar macrophage development in an IL-23- and GM-CSF-dependent manner. The apoptotic neutrophils could inhibit the secretion of IL-23 from alveolar macrophages, which is important for the production of GM-CSF, and depletion of neutrophils disrupted the regulation of IL-23 and GM-CSF. This study reveals a mechanism for the regulation of the local alveolar macrophage population and function by neutrophil apoptosis in the circulatory system.
引用
收藏
页码:1465 / 1474
页数:10
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