Abstract

Previously we demonstrated that ATP released from LPS-activated microglia induced IL-10 expression in a process involving P2 receptors, in an autocrine fashion. Therefore, in the present study we sought to determine which subtype of P2 receptor was responsible for the modulation of IL-10 expression in ATP-stimulated microglia. We found that the patterns of IL-10 production were dose-dependent (1, 10, 100, 1,000 microM) and bell-shaped. The concentrations of ATP, ATP-gammaS, ADP, and ADP-betaS that showed maximal IL-10 release were 100, 10, 100, and 100 microM respectively. The rank order of agonist potency for IL-10 production was 2'-3'-O-(4-benzoyl)-benzoyl ATP (BzATP)=dATP>2-methylthio-ADP (2-meSADP). On the other hand, 2-methylthio-ATP (2-meSATP), alpha,beta-methylene ATP (alpha,beta-meATP), UTP, and UDP did not induce the release of IL-10 from microglia. Further, we obtained evidence of crosstalk between P2 receptors, in a situation where intracellular Ca(2+) release and/or cAMP-activated PKA were the main contributors to extracellular ATP-(or ADP)-mediated IL-10 expression, and IL-10 production was down-regulated by either MRS2179 (a P2Y(1) antagonist) or 5'-AMPS (a P2Y(11) antagonist), indicating that both the P2Y(1) and P2Y(11) receptors are major receptors involved in IL-10 expression. In addition, we found that inhibition of IL-10 production by high concentrations of ATP-gammaS (100 microM) was restored by TNP-ATP (an antagonist of the P2X(1), P2X(3), and P2X(4) receptors), and that IL-10 production by 2-meSADP was restored by 2meSAMP (a P2Y(12) receptor antagonist) or pertussis toxin (PTX; a Gi protein inhibitor), indicating that the P2X(1), P2X(3), P2X(4)receptor group, or the P2Y(12) receptor, negatively modulate the P2Y(11) receptor or the P2Y(1) receptor, respectively.

Highlights

  • Extracellular purine (ATP, ADP) and pyrimidine (UTP, UDP) nucleotides mediate their effects via P2 receptors (Ralevic and Burnstock, 1998)

  • The P2Y1, P2Y2, P2Y4, P2Y6, and P2Y11 receptors are coupled to Gq, promoting PLCcatalyzed generation of an inositol phosphate (IP3) and subsequent release of intracellular calcium

  • We presented evidences for crosstalk between P2 receptors in a situation where P2Y1 and P2Y11 receptors are major receptors involved in extracellular ATP-(or ADP)-mediated IL-10 production, and P2X1, P2X3, P2X4 receptor group, or the P2Y12 receptor, negatively modulate the P2Y11 receptor or the P2Y1 receptor, respectively

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Summary

Introduction

Extracellular purine (ATP, ADP) and pyrimidine (UTP, UDP) nucleotides mediate their effects via P2 receptors (Ralevic and Burnstock, 1998). Stimulation of P2X receptors (P2X1P2X7) causes Ca2+ and Na+ influx from the extracellular space with accompanying plasma membrane depolarization (Khakh and North, 2006). The P2Y receptors are composed of eight subtypes in mammals: P2Y1, P2Y2, P2Y4, P2Y6, P2Y11, P2Y12, P2Y13, and P2Y14. The P2Y1, P2Y12, and P2Y13 receptors are preferentially activated by ADP whereas P2Y6 is activated by UDP (Abbracchio et al, 2006). The P2Y14 receptor is activated by the nucleotide sugar UDP-glucose (Brunschweiger and Muller, 2006). The P2Y1, P2Y2, P2Y4, P2Y6, and P2Y11 receptors are coupled to Gq, promoting PLCcatalyzed generation of an inositol phosphate (IP3) and subsequent release of intracellular calcium

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