GM-CSF-Dependent Inflammatory Pathways

被引:111
作者
Hamilton, John A. [1 ,2 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Parkville, Vic, Australia
[2] Univ Melbourne & Western Hlth, Australian Inst Musculoskeletal Sci AIMSS, St Albans, Vic, Australia
关键词
cell survival; polarization; inflammation; pain; IRF4; CCL17; COLONY-STIMULATING FACTOR; B-CELLS PROTECT; DENDRITIC CELLS; HUMAN-MONOCYTES; MACROPHAGE POLARIZATION; FETAL MONOCYTES; GROWTH-FACTOR; CYTOKINE; DIFFERENTIATION; ACTIVATION;
D O I
10.3389/fimmu.2019.02055
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pre-clinical models and clinical trials demonstrate that targeting the action of the cytokine, granulocyte macrophage-colony stimulating factor (GM-CSF), can be efficacious in inflammation/autoimmunity reinforcing the importance of understanding how GM-CSF functions; a significant GM-CSF-responding cell in this context is likely to be the monocyte. This article summarizes critically the literature on the downstream cellular pathways regulating GM-CSF interaction with monocytes (and macrophages), highlighting some contentious issues, and conclusions surrounding this biology. It also suggests future directions which could be undertaken so as to more fully understand this aspect of GM-CSF biology. Given the focus of this collection of articles on monocytes, the following discussion in general will be limited to this population or to its more mature progeny, the macrophage, even though GM-CSF biology is broader than this.
引用
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页数:8
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