IFN-γ up-regulates kappa opioid receptors (KOR) on murine macrophage cell line J774

被引:15
作者
Gabrilovac, Jelka [1 ]
Cupic, Barbara [1 ]
Zapletal, Emilija [1 ]
Brozovic, Anamaria [2 ]
机构
[1] Rudjer Boskovic Inst, Div Mol Med, Lab Expt Haematol Immunol & Oncol, HR-10002 Zagreb, Croatia
[2] Rudjer Boskovic Inst, Div Mol Biol, Lab Genotox Agents, HR-10002 Zagreb, Croatia
关键词
Kappa opioid receptors (KOR); IFN-gamma; J774; cells; Macrophages; Transcriptional expression; Protein expression; INTERFERON-GAMMA; IN-VITRO; T-CELLS; EXPRESSION; IMMUNE; DELTA; GENE; TRANSCRIPTION; MECHANISMS; INHIBITION;
D O I
10.1016/j.jneuroim.2012.02.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study we examined basal and IFN-gamma-regulated expression of kappa opioid receptors (KOR) on cells of a murine macrophage cell line, J774. Basal KOR expression was found both at transcriptional and protein levels. KOR protein was predominantly located intracellular (86.4 +/- 12.9% positive cells; n=4), and only in minority of J774 cells (9.1 +/- 6.4% positive cells; n=4) on plasma membranes, as revealed by Fluorescence-Activated Cell Sorter (FACS) analysis and immunocytochemistry. Proinflammatory cytokine IFN-gamma up-regulated KOR expression both at transcriptional (up to 24 times) and protein levels (up to 4.2 times). KOR expressed on J774 cells was functionally active as its ligation with Dynorphin-A(1-17) (100 nM and 1 mu M) triggered phosphotylation of ERK1/2. Involvement of KOR in the Dynorphin-A(1-17)-induced triggering of ERK1/2 phosphorylation is suggested since truncated Dynorphin-A(2-17), which does not bind to KOR, was ineffective. Collectively, we have shown for the first time that cells of J774 cell line constitutively express functionally active KOR, which triggers signalization via ERK1/2 phosphorylation and which could be up-regulated by proinflammatory IFN-gamma. The data may be relevant for better understanding of the role of KOR and their endogenous ligand Dynorphin-A in regulation of inflammatory and immune responses. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:56 / 65
页数:10
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