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Regulation of Gephyrin Cluster Size and Inhibitory Synaptic Currents on Renshaw Cells by Motor Axon Excitatory Inputs

 

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dc.creator González Forero, David es
dc.creator Pastor Loro, Ángel Manuel es
dc.creator Geiman, Eric J. es
dc.creator Benítez Temiño, Beatriz es
dc.creator Alvarez, Francisco J. es
dc.date.accessioned 2016-05-04T11:06:25Z
dc.date.available 2016-05-04T11:06:25Z
dc.date.issued 2005
dc.identifier.issn 0270-6474 es
dc.identifier.uri http://hdl.handle.net/11441/40719
dc.description.abstract Renshaw cells receive a high density of inhibitory synapses characterized by large postsynaptic gephyrin clusters and mixed glycinergic/ GABAergic inhibitory currents with large peak amplitudes and long decays. These properties appear adapted to increase inhibitory efficacy over Renshaw cells and mature postnatally by mechanisms that are unknown. We tested the hypothesis that heterosynaptic influences from excitatory motor axon inputs modulate the development of inhibitory synapses on Renshaw cells. Thus, tetanus (TeNT) and botulinum neurotoxin A (BoNT-A) were injected intramuscularly at postnatal day 5 (P5) to, respectively, elevate or reduce motor axon firing activity for 2 weeks. After TeNT injections, the average gephyrin cluster areas on Renshaw cells increased by 18.4% at P15 and 28.4% at P20 and decreased after BoNT-A injections by 17.7% at P15 and 19.9% at P20. The average size differences resulted from changes in the proportions of small and large gephyrin clusters. Whole-cell recordings in P9 –P15 Renshaw cells after P5 TeNT injections showed increases in the peak amplitude of glycinergic miniature postsynaptic currents (mPSCs) and the fast component of mixed (glycinergic/GABAergic) mPSCs compared with controls (60.9% and 78.9%, respectively). GABAergic mPSCs increased in peak amplitude to a smaller extent (45.8%). However, because of the comparatively longer decays of synaptic GABAergic currents, total current transfer changes after TeNT were similar for synaptic glycine and GABAA receptors (56 vs 48.9% increases, respectively). We concluded that motor axon excitatory synaptic activity modulates the development of inhibitory synapse properties on Renshaw cells, influencing recruitment of postsynaptic gephyrin and glycine receptors and, to lesser extent, GABAA receptors. es
dc.format application/pdf es
dc.language.iso eng es
dc.publisher Society for Neuroscience es
dc.relation.ispartof Journal of Neuroscience, 25(2), 417-429 es
dc.rights Attribution-NonCommercial-NoDerivatives 4.0 Internacional *
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/ *
dc.subject Motoneurons es
dc.subject Development es
dc.subject Spinal cord es
dc.subject Botulinum toxin es
dc.subject Tetanus toxin es
dc.subject GABAA receptor es
dc.subject Glycine receptor es
dc.subject Recurrent inhibition es
dc.title Regulation of Gephyrin Cluster Size and Inhibitory Synaptic Currents on Renshaw Cells by Motor Axon Excitatory Inputs es
dc.type info:eu-repo/semantics/article es
dc.type.version info:eu-repo/semantics/publishedVersion es
dc.rights.accessrights info:eu-repo/semantics/openAccess es
dc.contributor.affiliation Universidad de Sevilla. Departamento de Fisiología es
dc.relation.publisherversion http://www.jneurosci.org/content/25/2/417.full.pdf+html es
dc.identifier.doi http://dx.doi.org/10.1523/JNEUROSCI.3725-04.2005 es
idus.format.extent 13 es
dc.identifier.idus https://idus.us.es/xmlui/handle/11441/40719
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