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Axon‐glia communication evokes calcium signaling in olfactory ensheathing cells of the developing olfactory bulb
Author(s) -
Rieger Anne,
Deitmer Joachim W.,
Lohr Christian
Publication year - 2007
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.20460
Subject(s) - olfactory bulb , metabotropic glutamate receptor , biology , olfactory ensheathing glia , neuroscience , glutamate receptor , microbiology and biotechnology , olfactory system , stimulation , receptor , central nervous system , biochemistry
Olfactory ensheathing cells (OECs) accompany receptor axons in the olfactory nerve and promote axonal growth into the central nervous system. The mechanisms underlying the communication between axons and OECs, however, have not been studied in detail yet. We investigated the effect of activity‐dependent neuronal transmitter release on Ca 2+ signaling of OECs in acute mouse olfactory bulb slices using confocal Ca 2+ imaging. TTX‐sensitive axonal activity upon electrical nerve stimulation triggers a rise in cytosolic Ca 2+ in OECs, which can be mimicked by application of DHPG, an agonist of metabotropic glutamate receptors (mGluRs). Both stimulation‐ and DHPG‐induced Ca 2+ transients in OECs were abolished by depletion of intracellular Ca 2+ stores with cyclopiazonic acid (CPA). The mGluR 1 ‐specific antagonist CPCCOEt completely inhibited DHPG‐evoked Ca 2+ transients, but reduced stimulation‐induced Ca 2+ transients only partly, suggesting the involvement of another neurotransmitter. Application of ATP evoked CPA‐sensitive Ca 2+ transients in OECs, which were inhibited by the P2Y 1 ‐specific antagonist MRS2179. Co‐application of CPCCOEt and MRS2179 almost completely blocked the stimulation‐induced Ca 2+ transients, indicating that they were mediated by mGluR 1 and P2Y 1 receptors. Our results show that OECs are able to respond to olfactory nerve activity with an increase in cytosolic Ca 2+ due to glutamate and ATP release. © 2006 Wiley‐Liss, Inc.