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Published as doi: 10.1096/fj.07-101782.
(The FASEB Journal. 2008;22:2368-2378.)
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New evidence for purinergic signaling in the olfactory bulb: A2A and P2Y1 receptors mediate intracellular calcium release in astrocytes

Michael Doengi, Joachim W. Deitmer and Christian Lohr1

Abteilung für Allgemeine Zoologie, University of Kaiserslautern, Kaiserslautern, Germany

1Correspondence: Abteilung für Allgemeine Zoologie, University of Kaiserslautern, POB 3049, D-67653 Kaiserslautern, Germany. E-mail: clohr{at}biologie.uni-kl.de

Purinergic receptors play a key role in neuron-glia and glia-neuron interactions. In the present study, we have recorded cytosolic Ca2+ responses using confocal imaging in astrocytes of acute olfactory bulb slices from mice (postnatal days 3–8). By application of agonists and antagonists, we identified two types of receptors, P2Y1 and A2A, that mediated Ca2+ responses attributable to Ca2+ release from intracellular stores in the astrocytes. Both receptor types were activated by application of ATP and ADP; however, when enzymatic ATP degradation was suppressed by the alkaline phosphatase inhibitor levamisole, ATP only activated MRS2179-sensitive P2Y1 but not ZM241385-sensitive A2A receptors. The dose-response curve for A2A receptors activated by adenosine revealed an EC50 of 0.3 µM, one order of magnitude smaller than the EC50 of 5 µM determined for P2Y1 receptors activated by ADP. Electrical stimulation of the olfactory nerve in the presence of glutamate receptor blockers to suppress excitation of postsynaptic neurons evoked Ca2+ responses in most of the astrocytes, which were inhibited by blocking both P2Y1 and A2A receptors. Our results indicate that olfactory nerve terminals release not only glutamate, but also ATP, which activates P2Y1 receptors and, after degradation of ATP to adenosine, A2A receptors in astrocytes.—Doengi, M., Deitmer, J. W., Lohr, C. New evidence for purinergic signaling in the olfactory bulb: A2A and P2Y1 receptors mediate intracellular calcium release in astrocytes.


Key Words: neuron-glia interaction • adenosine triphosphate







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