Recycling endosome-dependent and -independent mechanisms for IL-10 secretion in LPS-activated macrophages

被引:35
|
作者
Stanley, A. C. [1 ]
Lieu, Z. Z. [2 ,3 ]
Wall, A. A. [1 ]
Venturato, J. [1 ]
Khromykh, T. [1 ]
Hamilton, N. A. [1 ]
Gleeson, P. A. [2 ,3 ]
Stow, J. L. [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Melbourne, Dept Biochem & Mol Biol, Melbourne, Vic 3010, Australia
[3] Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会;
关键词
cytokines; trafficking; secretion; TRANS-GOLGI NETWORK; CYTOKINE SECRETION; PLASMA-MEMBRANE; INTERLEUKIN-10-DEFICIENT MICE; IMMUNE-SYSTEM; E-CADHERIN; T-CELLS; B-CELL; PATHWAY; TRAFFICKING;
D O I
10.1189/jlb.0412191
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
IL-10 is a key anti-inflammatory cytokine secreted by activated macrophages as a feedback control mechanism to prevent excessive inflammatory responses. Here, we define multiple intracellular trafficking pathways involved in the secretion of newly synthesized IL-10 from macrophages following TLR4 activation with LPS, and show how this relates to the previously defined trafficking pathways for IL-6 and TNF in macrophages simultaneously producing these proinflammatory cytokines. IL-10 exits the Golgi in multiple tubular carriers, including those dependent on p230GRIP. Some of the IL-10 is then delivered to recycling endosomes, where cytokine sorting may occur prior to its release. Another portion of the IL-10 is delivered to the cell surface in distinct vesicles colabeled for apoE. Thus, we show at least two post-Golgi pathways via which IL-10 is trafficked, ensuring its secretion from activated macrophages under different physiological conditions. J. Leukoc. Biol. 92: 1227-1239; 2012.
引用
收藏
页码:1227 / 1239
页数:13
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