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Activity-Dependent Synaptic Refinement: New Insights from Drosophila

During development, neurons establish inappropriate connections as they seek out their synaptic partners, resulting in supernumerary synapses that must be pruned away. The removal of miswired synapses usually involves electrical activity, often through a Hebbian spike-timing mechanism. A novel form...

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Autores principales: Vonhoff, Fernando, Keshishian, Haig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399093/
https://www.ncbi.nlm.nih.gov/pubmed/28484377
http://dx.doi.org/10.3389/fnsys.2017.00023
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author Vonhoff, Fernando
Keshishian, Haig
author_facet Vonhoff, Fernando
Keshishian, Haig
author_sort Vonhoff, Fernando
collection PubMed
description During development, neurons establish inappropriate connections as they seek out their synaptic partners, resulting in supernumerary synapses that must be pruned away. The removal of miswired synapses usually involves electrical activity, often through a Hebbian spike-timing mechanism. A novel form of activity-dependent refinement is used by Drosophila that may be non-Hebbian, and is critical for generating the precise connectivity observed in that system. In Drosophila, motoneurons use both glutamate and the biogenic amine octopamine for neurotransmission, and the muscle fibers receive multiple synaptic inputs. Motoneuron growth cones respond in a time-regulated fashion to multiple chemotropic signals arising from their postsynaptic partners. Central to this mechanism is a very low frequency (<0.03 Hz) oscillation of presynaptic cytoplasmic calcium, that regulates and coordinates the action of multiple downstream effectors involved in the withdrawal from off-target contacts. Low frequency calcium oscillations are widely observed in developing neural circuits in mammals, and have been shown to be critical for normal connectivity in a variety of neural systems. In Drosophila these mechanisms allow the growth cone to sample widely among possible synaptic partners, evaluate opponent chemotropic signals, and withdraw from off-target contacts. It is possible that the underlying molecular mechanisms are conserved widely among invertebrates and vertebrates.
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spelling pubmed-53990932017-05-08 Activity-Dependent Synaptic Refinement: New Insights from Drosophila Vonhoff, Fernando Keshishian, Haig Front Syst Neurosci Neuroscience During development, neurons establish inappropriate connections as they seek out their synaptic partners, resulting in supernumerary synapses that must be pruned away. The removal of miswired synapses usually involves electrical activity, often through a Hebbian spike-timing mechanism. A novel form of activity-dependent refinement is used by Drosophila that may be non-Hebbian, and is critical for generating the precise connectivity observed in that system. In Drosophila, motoneurons use both glutamate and the biogenic amine octopamine for neurotransmission, and the muscle fibers receive multiple synaptic inputs. Motoneuron growth cones respond in a time-regulated fashion to multiple chemotropic signals arising from their postsynaptic partners. Central to this mechanism is a very low frequency (<0.03 Hz) oscillation of presynaptic cytoplasmic calcium, that regulates and coordinates the action of multiple downstream effectors involved in the withdrawal from off-target contacts. Low frequency calcium oscillations are widely observed in developing neural circuits in mammals, and have been shown to be critical for normal connectivity in a variety of neural systems. In Drosophila these mechanisms allow the growth cone to sample widely among possible synaptic partners, evaluate opponent chemotropic signals, and withdraw from off-target contacts. It is possible that the underlying molecular mechanisms are conserved widely among invertebrates and vertebrates. Frontiers Media S.A. 2017-04-21 /pmc/articles/PMC5399093/ /pubmed/28484377 http://dx.doi.org/10.3389/fnsys.2017.00023 Text en Copyright © 2017 Vonhoff and Keshishian. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Vonhoff, Fernando
Keshishian, Haig
Activity-Dependent Synaptic Refinement: New Insights from Drosophila
title Activity-Dependent Synaptic Refinement: New Insights from Drosophila
title_full Activity-Dependent Synaptic Refinement: New Insights from Drosophila
title_fullStr Activity-Dependent Synaptic Refinement: New Insights from Drosophila
title_full_unstemmed Activity-Dependent Synaptic Refinement: New Insights from Drosophila
title_short Activity-Dependent Synaptic Refinement: New Insights from Drosophila
title_sort activity-dependent synaptic refinement: new insights from drosophila
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399093/
https://www.ncbi.nlm.nih.gov/pubmed/28484377
http://dx.doi.org/10.3389/fnsys.2017.00023
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