Evidence for functional adenosine A3 receptors in microglia cells

被引:81
作者
Hammarberg, C [1 ]
Schulte, G [1 ]
Fredholm, BB [1 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, Mol Pharmacol Sect, S-17177 Stockholm, Sweden
关键词
ERK1/2; G protein-coupled receptor; mitogen-activated protein kinase; N13; cells; protein phosphorylation;
D O I
10.1046/j.1471-4159.2003.01919.x
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
Adenosine exerts its effects through four subtypes of G-protein-coupled receptors (GPCRs): adenosine A(1) and A(3) receptors (A(3) R), which generally couple to G(i) proteins and adenosine A(2A) and A(2B) receptors that activate G(s) proteins. Though there is evidence for the expression of mRNA for the A(3) R in the central nervous system, evidence for functional receptors has depended on drugs with uncertain specificity. Here, we show that A(3) Rs mediating functional responses are present in microglia cells. By selectively stimulating the A(3) R in both primary mouse microglia cells and the N13 microglia cell line with the agonist Cl-IB-MECA, we have found a biphasic, partly G(i) protein-dependent influence on the phosphorylation of the extracellular signal-regulated protein kinase 1/2 (ERK1/2). ERK1/2 activation was assessed by immunoblotting with phospho-specific antibodies. The involvement of the A(3) R in Cl-IB-MECA-induced ERK1/2 phosphorylation was confirmed by demonstrating that those effects are absent in primary mouse microglia cells isolated from mice lacking the gene for the A(3) R.
引用
收藏
页码:1051 / 1054
页数:4
相关论文
共 35 条
[1]  
Abbracchio MP, 1995, MOL PHARMACOL, V48, P1038
[2]   IMMORTALIZATION OF MURINE MICROGLIAL CELLS BY A V-RAF/V-MYC CARRYING RETROVIRUS [J].
BLASI, E ;
BARLUZZI, R ;
BOCCHINI, V ;
MAZZOLLA, R ;
BISTONI, F .
JOURNAL OF NEUROIMMUNOLOGY, 1990, 27 (2-3) :229-237
[3]   Assignment of ecto-nucleoside triphosphate diphosphohydrolase-1/cd39 expression to microglia and vasculature of the brain [J].
Braun, N ;
Sévigny, J ;
Robson, SC ;
Enjyoji, K ;
Guckelberger, O ;
Hammer, K ;
Di Virgilio, F ;
Zimmermann, H .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (12) :4357-4366
[4]   Microglia as liaisons between the immune and central nervous systems: Functional implications for multiple sclerosis [J].
Carson, MJ .
GLIA, 2002, 40 (02) :218-231
[5]  
Dalmau I, 1998, J COMP NEUROL, V398, P333, DOI 10.1002/(SICI)1096-9861(19980831)398:3<333::AID-CNE3>3.0.CO
[6]  
2-0
[7]   Induction of potassium channels in mouse brain microglia: Cells acquire responsiveness to pneumococcal cell wall components during late development [J].
Draheim, HJ ;
Prinz, M ;
Weber, JR ;
Weiser, T ;
Kettenmann, H ;
Hanisch, UK .
NEUROSCIENCE, 1999, 89 (04) :1379-1390
[8]   Hematopoietic cells differentiate into both microglia and macroglia in the brains of adult mice [J].
Eglitis, MA ;
Mezey, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :4080-4085
[9]   REGIONAL DIFFERENCES IN THE EFFECT OF GUANINE-NUCLEOTIDES ON AGONIST AND ANTAGONIST BINDING TO ADENOSINE A1-RECEPTORS IN RAT-BRAIN, AS REVEALED BY AUTORADIOGRAPHY [J].
FASTBOM, J ;
FREDHOLM, BB .
NEUROSCIENCE, 1990, 34 (03) :759-769
[10]  
Ferrari D, 1996, J IMMUNOL, V156, P1531