IL-6 inhibits IFN-γ induced autophagy in Mycobacterium tuberculosis H37Rv infected macrophages

被引:136
作者
Dutta, Rajesh Kumar [1 ]
Kathania, Mahesh [1 ]
Raje, Manoj [1 ]
Majumdar, Sekhar [1 ]
机构
[1] CSIR, Inst Microbial Technol, Div Cell Biol & Immunol, Chandigarh 160036, India
关键词
Autophagy; IFN-gamma; IL-6; Mycobacteria; SIGNALING PATHWAYS; MAMMALIAN-CELLS; INNATE IMMUNITY; INTERLEUKIN-6; RESPONSES; IMMUNOLOGY; SURVIVAL; DEFENSE;
D O I
10.1016/j.biocel.2012.02.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The significance of IL-6 production in tuberculosis is yet to be fully elucidated, although it is known for quite some time that IL-6 interferes with IFN-gamma induced signal. In order to know which cellular process induced by IFN-gamma is actually counteracted by IL-6, we studied the role of IL-6 on IFN-gamma induced autophagy formation in virulent Mycobacterium tuberculosis infection in THP-1 cells, since it is well characterized that induction of autophagy by IFN-gamma eliminates intracellular mycobacterium by overcoming the phagosome maturation block imposed by bacilli. We report here that IL-6 inhibits both IFN-gamma and starvation induced autophagy in M. tuberculosis H37Rv infected cells. M. tuberculosis H37Rv infection results in time dependent production of IL-6 in THP-1 cells and neutralization of this endogenous IL-6 by anti-IL-6 antibody significantly enhances the IFN-gamma mediated killing of the intracellular bacteria. IL-6 time dependently lowers Atg12-Atg5 complex and therefore inhibits autophagosome biogenesis rather than autophagolysosome formation. IL-6 also affects IFN-gamma mediated stimulation of mTOR, p-38 and JNK pathways. These results clearly indicate that virulent mycobacteria strategically upregulate IL-6 production to combat innate immunity. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:942 / 954
页数:13
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