GM-CSF and IL-4 produced by NKT cells inversely regulate IL-1β production by macrophages

被引:21
作者
Ahn, Sehee [2 ]
Jeong, Dongjin [2 ]
Oh, Sae Jin [2 ]
Ahn, Jiye [2 ]
Lee, Seung Hyo [4 ]
Chung, Doo Hyun [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Dept Pathol, Coll Med, 103 Daehak Ro, Seoul 110799, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Biomed Sci, Lab Immune Regulat, Seoul, South Korea
[3] Seoul Natl Univ, Coll Med, Ischem Hypoxia Inst, Seoul, South Korea
[4] Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Biomed Res Ctr, Daejeon 305701, South Korea
关键词
NKT cells; Macrophages; IL-lb; GM-CSF; IL-4; ACTIVATION; CYTOKINE; SUBSETS; BIOLOGY; BETA;
D O I
10.1016/j.imlet.2017.01.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural Killer T(NKT) cells are distinct T cell subset that link innate and adaptive immune responses. IL-1 beta , produced by various immune cells, plays a key role in the regulation of innate immunity in vivo. However, it is unclear whether NKT cells regulate IL-1 beta production by macrophages. To address this, we co-cultured NKT cells and peritoneal macrophages in the presence of TCR stimulation and inflammasome activators. Among cytokines secreted from NKT cells, GM-CSF enhanced IL-1 beta production by macrophages via regulating LPS-mediated pro-IL-1 beta expression and NLRP3-dependent inflammasome activation, whereas IL-4 enhanced M2-differentiation of macrophages and decreased IL-1 beta production. Together, our findings suggest the NKT cells have double-sided effects on IL-1 beta-mediated innate immune responses by producing IL-4 and GM-CSF. These findings may be helpful for a comprehensive understanding of NKT cell-mediated regulatory mechanisms of the pro-inflammatory effects of IL-1 beta in inflammatory diseases in vivo. (C)2017 European Federation of Immunological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:50 / 56
页数:7
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