Combinations of TLR and NOD2 ligands stimulate rat microglial P2X4R expression

被引:35
作者
Guo, Liang-Hao
Guo, Ke-Tai
Wendel, Hans Peter
Schluesener, Hermann J.
机构
[1] Univ Tubingen, Brain Res Inst, D-72076 Tubingen, Germany
[2] Univ Tubingen Hosp, Dept Thorac Cardiac & Vasc Surg, D-72076 Tubingen, Germany
关键词
microglia; P2X4; receptor; toll-like receptors; muramyldipeptide; innate immune system; CNS; TOLL-LIKE RECEPTORS; LIPOTEICHOIC ACID; P2X(4) RECEPTOR; UP-REGULATION; STRANDED-RNA; CELLS; ACTIVATION; RELEASE; LIPOPOLYSACCHARIDE; RECOGNITION;
D O I
10.1016/j.bbrc.2006.08.146
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
As ATP-gated ion channels, P2X4 receptors (P2X4R) of microglial cells play a crucial role in central nervous system (CNS) inflammation. In this study, we used rat microglial cell cultures to examine P2X4R expression in response to stimulation by combination of toll-like receptors (TLRs) and nucleotide-binding oligomerization domain 2 (NOD2) receptors. Various TLR1-9 ligands and NOD2 agonist muramyldipeptide (MDP) were investigated. Our results showed that certain combination of ligands had additive effects on upregulating microglial P2X4R at both mRNA and protein levels, and induced nitric oxide increase and tumor necrosis factor-alpha production. Thus TLRs and NOD2 combinations are contributors to the signaling cascades resulting in purinergic microglial activation. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1156 / 1162
页数:7
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