Interleukin-10 Alters Effector Functions of Multiple Genes Induced by Borrelia burgdorferi in Macrophages To Regulate Lyme Disease Inflammation

被引:47
作者
Gautam, Aarti
Dixit, Saurabh
Philipp, Mario T.
Singh, Shree R.
Morici, Lisa A. [3 ]
Kaushal, Deepak [2 ]
Dennis, Vida A. [1 ]
机构
[1] Alabama State Univ, Dept Biol Sci, PhD Program Microbiol, Ctr Nanobiotechnol Res, Montgomery, AL 36104 USA
[2] Tulane Univ, Div Bacteriol & Parasitol, Tulane Natl Primate Res Ctr, Hlth Sci Ctr,Dept Bacteriol & Parasitol, Covington, LA 70433 USA
[3] Tulane Univ, Hlth Sci Ctr, Dept Microbiol & Immunol, New Orleans, LA 70118 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
TOLL-LIKE RECEPTOR-2; NF-KAPPA-B; CHEMOATTRACTANT PROTEIN-1 PRODUCTION; INNATE IMMUNE ACTIVATION; HOST-DEFENSE MECHANISMS; NECROSIS-FACTOR-ALPHA; HUMAN MONOCYTIC CELLS; MIGRANS SKIN-LESIONS; TREPONEMA-PALLIDUM; ERYTHEMA MIGRANS;
D O I
10.1128/IAI.05451-11
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin-10 (IL-10) modulates inflammatory responses elicited in vitro and in vivo by Borrelia burgdorferi, the Lyme disease spirochete. How IL-10 modulates these inflammatory responses still remains elusive. We hypothesize that IL-10 inhibits effector functions of multiple genes induced by B. burgdorferi in macrophages to control concomitantly elicited inflammation. Because macrophages are essential in the initiation of inflammation, we used mouse J774 macrophages and live B. burgdorferi spirochetes as the model target cell and stimulant, respectively. First, we employed transcriptome profiling to identify genes that were induced by stimulation of cells with live spirochetes and that were perturbed by addition of IL-10 to spirochete cultures. Spirochetes significantly induced upregulation of 347 genes at both the 4-h and 24-h time points. IL-10 inhibited the expression levels, respectively, of 53 and 65 of the 4-h and 24-h genes, and potentiated, respectively, at 4 h and 24 h, 65 and 50 genes. Prominent among the novel identified IL-10-inhibited genes also validated by quantitative real-time PCR (qRT-PCR) were Toll-like receptor 1 (TLR1), TLR2, IRAK3, TRAF1, IRG1, PTGS2, MMP9, IFI44, IFIT1, and CD40. Proteome analysis using a multiplex enzyme-linked immunosorbent assay (ELISA) revealed the IL-10 modulation/and or potentiation of RANTES/CCL5, macrophage inflammatory protein 2 (MIP-2)/CXCL2, IP-10/CXCL10, MIP-1 alpha/CCL3, granulocyte colony-stimulating factor (G-CSF)/CSF3, CXCL1, CXCL5, CCL2, CCL4, IL-6, tumor necrosis factor alpha (TNF-alpha), IL-1 alpha, IL-1 beta, gamma interferon (IFN-gamma), and IL-9. Similar results were obtained using sonicated spirochetes or lipoprotein as stimulants. Our data show that IL-10 alters effectors induced by B. burgdorferi in macrophages to control concomitantly elicited inflammatory responses. Moreover, for the first time, this study provides global insight into potential mechanisms used by IL-10 to control Lyme disease inflammation.
引用
收藏
页码:4876 / 4892
页数:17
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