| Literature DB >> 26881904 |
Feng Tian1, Yong Han1, Jian Song2, Jie Lei1, Xiaolong Yan1, Nianlin Xie1, Jian Wang1, Jinbo Zhao1, Xiaohua Liang1, Daixing Zhong1, Yongan Zhou1, Xiaoping Wang1, Xiaofei Li1.
Abstract
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.Entities:
Keywords: CD18; GM-CSF; IL-23; alveolar macrophages; neutrophils
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Year: 2016 PMID: 26881904 DOI: 10.1111/febs.13684
Source DB: PubMed Journal: FEBS J ISSN: 1742-464X Impact factor: 5.542