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Developmental regulation of CB1-mediated spike-time dependent depression at immature mossy fiber-CA3 synapses

Early in postnatal life, mossy fibres (MF), the axons of granule cells in the dentate gyrus, release GABA which is depolarizing and excitatory. Synaptic currents undergo spike-time dependent long-term depression (STD-LTD) regardless of the temporal order of stimulation (pre versus post and viceversa...

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Autores principales: Caiati, Maddalena D., Sivakumaran, Sudhir, Lanore, Frederic, Mulle, Christophe, Richard, Elodie, Verrier, Dany, Marsicano, Giovanni, Miles, Richard, Cherubini, Enrico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285903/
https://www.ncbi.nlm.nih.gov/pubmed/22368777
http://dx.doi.org/10.1038/srep00285
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author Caiati, Maddalena D.
Sivakumaran, Sudhir
Lanore, Frederic
Mulle, Christophe
Richard, Elodie
Verrier, Dany
Marsicano, Giovanni
Miles, Richard
Cherubini, Enrico
author_facet Caiati, Maddalena D.
Sivakumaran, Sudhir
Lanore, Frederic
Mulle, Christophe
Richard, Elodie
Verrier, Dany
Marsicano, Giovanni
Miles, Richard
Cherubini, Enrico
author_sort Caiati, Maddalena D.
collection PubMed
description Early in postnatal life, mossy fibres (MF), the axons of granule cells in the dentate gyrus, release GABA which is depolarizing and excitatory. Synaptic currents undergo spike-time dependent long-term depression (STD-LTD) regardless of the temporal order of stimulation (pre versus post and viceversa). Here we show that at P3 but not at P21, STD-LTD, induced by negative pairing, is mediated by endocannabinoids mobilized from the postsynaptic cell during spiking-induced membrane depolarization. By diffusing backward, endocannabinoids activate cannabinoid type-1 (CB1) receptors probably expressed on MF. Thus, STD-LTD was prevented by CB1 receptor antagonists and was absent in CB1-KO mice. Consistent with these data, in situ hybridization experiments revealed detectable level of CB1 mRNA in the granule cell layer at P3 but not at P21. These results indicate that CB1 receptors are transiently expressed on immature MF terminals where they counteract the enhanced neuronal excitability induced by the excitatory action of GABA.
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spelling pubmed-32859032012-02-24 Developmental regulation of CB1-mediated spike-time dependent depression at immature mossy fiber-CA3 synapses Caiati, Maddalena D. Sivakumaran, Sudhir Lanore, Frederic Mulle, Christophe Richard, Elodie Verrier, Dany Marsicano, Giovanni Miles, Richard Cherubini, Enrico Sci Rep Article Early in postnatal life, mossy fibres (MF), the axons of granule cells in the dentate gyrus, release GABA which is depolarizing and excitatory. Synaptic currents undergo spike-time dependent long-term depression (STD-LTD) regardless of the temporal order of stimulation (pre versus post and viceversa). Here we show that at P3 but not at P21, STD-LTD, induced by negative pairing, is mediated by endocannabinoids mobilized from the postsynaptic cell during spiking-induced membrane depolarization. By diffusing backward, endocannabinoids activate cannabinoid type-1 (CB1) receptors probably expressed on MF. Thus, STD-LTD was prevented by CB1 receptor antagonists and was absent in CB1-KO mice. Consistent with these data, in situ hybridization experiments revealed detectable level of CB1 mRNA in the granule cell layer at P3 but not at P21. These results indicate that CB1 receptors are transiently expressed on immature MF terminals where they counteract the enhanced neuronal excitability induced by the excitatory action of GABA. Nature Publishing Group 2012-02-24 /pmc/articles/PMC3285903/ /pubmed/22368777 http://dx.doi.org/10.1038/srep00285 Text en Copyright © 2012, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Caiati, Maddalena D.
Sivakumaran, Sudhir
Lanore, Frederic
Mulle, Christophe
Richard, Elodie
Verrier, Dany
Marsicano, Giovanni
Miles, Richard
Cherubini, Enrico
Developmental regulation of CB1-mediated spike-time dependent depression at immature mossy fiber-CA3 synapses
title Developmental regulation of CB1-mediated spike-time dependent depression at immature mossy fiber-CA3 synapses
title_full Developmental regulation of CB1-mediated spike-time dependent depression at immature mossy fiber-CA3 synapses
title_fullStr Developmental regulation of CB1-mediated spike-time dependent depression at immature mossy fiber-CA3 synapses
title_full_unstemmed Developmental regulation of CB1-mediated spike-time dependent depression at immature mossy fiber-CA3 synapses
title_short Developmental regulation of CB1-mediated spike-time dependent depression at immature mossy fiber-CA3 synapses
title_sort developmental regulation of cb1-mediated spike-time dependent depression at immature mossy fiber-ca3 synapses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285903/
https://www.ncbi.nlm.nih.gov/pubmed/22368777
http://dx.doi.org/10.1038/srep00285
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