Differential changes in GPR55 during microglial cell activation

被引:99
作者
Pietr, Maciej [1 ]
Kozela, Ewa [1 ]
Levy, Rivka [1 ]
Rimmerman, Neta [1 ]
Lin, Yi Hsing [2 ,3 ]
Stella, Nephi [2 ,3 ]
Vogel, Zvi [1 ,4 ]
Juknat, Ana [4 ]
机构
[1] Weizmann Inst Sci, Dept Neurobiol, IL-76100 Rehovot, Israel
[2] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA
[4] Tel Aviv Univ, Sackler Fac Med, Dr Miriam & Sheldon G Adelson Ctr Biol Addict Dis, Tel Aviv, Israel
关键词
Cannabinoid; Microglia; Lipopolysaccharide; Interferon gamma; G protein-coupled receptor 55; CB2; receptor; Lysophosphatidylinositol; ERK phosphorylation; CB2 CANNABINOID RECEPTOR; EXPRESSION; BRAIN; ANANDAMIDE; GAMMA;
D O I
10.1016/j.febslet.2009.05.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We examined how lipopolysaccharide (LPS) and interferon gamma (IFN-gamma), known to differentially activate microglia, affect the expression of G protein-coupled receptor 55 (GPR55), a novel cannabinoid receptor. We found that GPR55 mRNA is significantly expressed in both primary mouse microglia and the BV-2 mouse microglial cell line, and that LPS down-regulates this message. Conversely, IFN-gamma slightly decreases GPR55 mRNA in primary microglia, while it upregulates this message in BV-2 cells. Moreover, the GPR55 agonist, lysophosphatidylinositol, increases ERK phosphorylation in BV-2 stimulated with IFN-gamma, in correlation with the increased amount of GPR55 mRNA. Remarkably, these stimuli-induced changes in GPR55 expression are similar to those observed with CB2-R, suggesting that both receptors might be involved in neuroinflammation and that their expression is concomitantly controlled by the state of microglial activation. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:2071 / 2076
页数:6
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