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Visual Stimulation Activates ERK in Synaptic and Somatic Compartments of Rat Cortical Neurons with Parallel Kinetics

BACKGROUND: Extracellular signal-regulated kinase (ERK) signalling pathway plays a crucial role in regulating diverse neuronal processes, such as cell proliferation and differentiation, and long-term synaptic plasticity. However, a detailed understanding of the action of ERK in neurons is made diffi...

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Autores principales: Boggio, Elena M., Putignano, Elena, Sassoè-Pognetto, Marco, Pizzorusso, Tommaso, Giustetto, Maurizio
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1899229/
https://www.ncbi.nlm.nih.gov/pubmed/17622349
http://dx.doi.org/10.1371/journal.pone.0000604
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author Boggio, Elena M.
Putignano, Elena
Sassoè-Pognetto, Marco
Pizzorusso, Tommaso
Giustetto, Maurizio
author_facet Boggio, Elena M.
Putignano, Elena
Sassoè-Pognetto, Marco
Pizzorusso, Tommaso
Giustetto, Maurizio
author_sort Boggio, Elena M.
collection PubMed
description BACKGROUND: Extracellular signal-regulated kinase (ERK) signalling pathway plays a crucial role in regulating diverse neuronal processes, such as cell proliferation and differentiation, and long-term synaptic plasticity. However, a detailed understanding of the action of ERK in neurons is made difficult by the lack of knowledge about its subcellular localization in response to physiological stimuli. To address this issue, we have studied the effect of visual stimulation in vivo of dark-reared rats on the spatial-temporal dynamics of ERK activation in pyramidal neurons of the visual cortex. METHODOLOGY/PRINCIPAL FINDINGS: Using immunogold electron microscopy, we show that phosphorylated ERK (pERK) is present in dendritic spines, both at synaptic and non-synaptic plasma membrane domains. Moreover, pERK is also detected in presynaptic axonal boutons forming connections with dendritic spines. Visual stimulation after dark rearing during the critical period causes a rapid increase in the number of pERK-labelled synapses in cortical layers I–II/III. This visually-induced activation of ERK at synaptic sites occurs in pre- and post-synaptic compartments and its temporal profile is identical to that of ERK activation in neuronal cell bodies. CONCLUSIONS/SIGNIFICANCE: Visual stimulation in vivo increases pERK expression at pre- and post-synaptic sites of axo-spinous junctions, suggesting that ERK plays an important role in the local modulation of synaptic function. The data presented here support a model in which pERK can have early and late actions both centrally in the cell nucleus and peripherally at synaptic contacts.
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spelling pubmed-18992292007-07-11 Visual Stimulation Activates ERK in Synaptic and Somatic Compartments of Rat Cortical Neurons with Parallel Kinetics Boggio, Elena M. Putignano, Elena Sassoè-Pognetto, Marco Pizzorusso, Tommaso Giustetto, Maurizio PLoS One Research Article BACKGROUND: Extracellular signal-regulated kinase (ERK) signalling pathway plays a crucial role in regulating diverse neuronal processes, such as cell proliferation and differentiation, and long-term synaptic plasticity. However, a detailed understanding of the action of ERK in neurons is made difficult by the lack of knowledge about its subcellular localization in response to physiological stimuli. To address this issue, we have studied the effect of visual stimulation in vivo of dark-reared rats on the spatial-temporal dynamics of ERK activation in pyramidal neurons of the visual cortex. METHODOLOGY/PRINCIPAL FINDINGS: Using immunogold electron microscopy, we show that phosphorylated ERK (pERK) is present in dendritic spines, both at synaptic and non-synaptic plasma membrane domains. Moreover, pERK is also detected in presynaptic axonal boutons forming connections with dendritic spines. Visual stimulation after dark rearing during the critical period causes a rapid increase in the number of pERK-labelled synapses in cortical layers I–II/III. This visually-induced activation of ERK at synaptic sites occurs in pre- and post-synaptic compartments and its temporal profile is identical to that of ERK activation in neuronal cell bodies. CONCLUSIONS/SIGNIFICANCE: Visual stimulation in vivo increases pERK expression at pre- and post-synaptic sites of axo-spinous junctions, suggesting that ERK plays an important role in the local modulation of synaptic function. The data presented here support a model in which pERK can have early and late actions both centrally in the cell nucleus and peripherally at synaptic contacts. Public Library of Science 2007-07-11 /pmc/articles/PMC1899229/ /pubmed/17622349 http://dx.doi.org/10.1371/journal.pone.0000604 Text en Boggio et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Boggio, Elena M.
Putignano, Elena
Sassoè-Pognetto, Marco
Pizzorusso, Tommaso
Giustetto, Maurizio
Visual Stimulation Activates ERK in Synaptic and Somatic Compartments of Rat Cortical Neurons with Parallel Kinetics
title Visual Stimulation Activates ERK in Synaptic and Somatic Compartments of Rat Cortical Neurons with Parallel Kinetics
title_full Visual Stimulation Activates ERK in Synaptic and Somatic Compartments of Rat Cortical Neurons with Parallel Kinetics
title_fullStr Visual Stimulation Activates ERK in Synaptic and Somatic Compartments of Rat Cortical Neurons with Parallel Kinetics
title_full_unstemmed Visual Stimulation Activates ERK in Synaptic and Somatic Compartments of Rat Cortical Neurons with Parallel Kinetics
title_short Visual Stimulation Activates ERK in Synaptic and Somatic Compartments of Rat Cortical Neurons with Parallel Kinetics
title_sort visual stimulation activates erk in synaptic and somatic compartments of rat cortical neurons with parallel kinetics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1899229/
https://www.ncbi.nlm.nih.gov/pubmed/17622349
http://dx.doi.org/10.1371/journal.pone.0000604
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