| Literature DB >> 25260706 |
Marta Gómez-Gonzalo1, Marta Navarrete2, Gertrudis Perea1, Ana Covelo3, Mario Martín-Fernández3, Ryuichi Shigemoto4, Rafael Luján5, Alfonso Araque6.
Abstract
Endocannabinoids (eCBs) play key roles in brain function, acting as modulatory signals in synaptic transmission and plasticity. They are recognized as retrograde messengers that mediate long-term synaptic depression (LTD), but their ability to induce long-term potentiation (LTP) is poorly known. We show that eCBs induce the long-term enhancement of transmitter release at single hippocampal synapses through stimulation of astrocytes when coincident with postsynaptic activity. This LTP requires the coordinated activity of the 3 elements of the tripartite synapse: 1) eCB-evoked astrocyte calcium signal that stimulates glutamate release; 2) postsynaptic nitric oxide production; and 3) activation of protein kinase C and presynaptic group I metabotropic glutamate receptors, whose location at presynaptic sites was confirmed by immunoelectron microscopy. Hence, while eCBs act as retrograde signals to depress homoneuronal synapses, they serve as lateral messengers to induce LTP in distant heteroneuronal synapses through stimulation of astrocytes. Therefore, eCBs can trigger LTP through stimulation of astrocyte-neuron signaling, revealing novel cellular mechanisms of eCB effects on synaptic plasticity.Entities:
Keywords: LTP; astrocytes; endocannabinoid signaling; mGluRs; nitric oxide
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Year: 2014 PMID: 25260706 DOI: 10.1093/cercor/bhu231
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 5.357