Cargando…

Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease

Experience-induced expression of immediate-early gene Arc/Arg3.1 is known to play a pivotal role in the consolidation of memory. Here we use in-vivo longitudinal multiphoton imaging to show orchestrated activity-dependent expression of Arc in the mouse extrastriate visual cortex in response to a str...

Descripción completa

Detalles Bibliográficos
Autores principales: Rudinskiy, Nikita, Hawkes, Jonathan M., Betensky, Rebecca A., Eguchi, Megumi, Yamaguchi, Shun, Spires-Jones, Tara L., Hyman, Bradley T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458168/
https://www.ncbi.nlm.nih.gov/pubmed/22922786
http://dx.doi.org/10.1038/nn.3199
_version_ 1782244633465585664
author Rudinskiy, Nikita
Hawkes, Jonathan M.
Betensky, Rebecca A.
Eguchi, Megumi
Yamaguchi, Shun
Spires-Jones, Tara L.
Hyman, Bradley T.
author_facet Rudinskiy, Nikita
Hawkes, Jonathan M.
Betensky, Rebecca A.
Eguchi, Megumi
Yamaguchi, Shun
Spires-Jones, Tara L.
Hyman, Bradley T.
author_sort Rudinskiy, Nikita
collection PubMed
description Experience-induced expression of immediate-early gene Arc/Arg3.1 is known to play a pivotal role in the consolidation of memory. Here we use in-vivo longitudinal multiphoton imaging to show orchestrated activity-dependent expression of Arc in the mouse extrastriate visual cortex in response to a structured visual stimulation. In wild-type mice, the amplitude of the Arc response in individual neurons strongly predicts the probability of reactivation by a subsequent presentation of the same stimulus. In a mouse model of Alzheimer’s disease, this association is markedly disrupted in the cortex specifically near senile plaques. Neurons in the vicinity of plaques are less likely to respond but, paradoxically, there is stronger response in those few neurons around plaques that do respond. To the extent that the orchestrated pattern of Arc expression reflects nervous system responses to, and physiological consolidation of, behavioral experience, the disruption in Arc patterns reveals plaque-associated interference with neural network integration.
format Online
Article
Text
id pubmed-3458168
institution National Center for Biotechnology Information
language English
publishDate 2012
record_format MEDLINE/PubMed
spelling pubmed-34581682013-04-01 Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease Rudinskiy, Nikita Hawkes, Jonathan M. Betensky, Rebecca A. Eguchi, Megumi Yamaguchi, Shun Spires-Jones, Tara L. Hyman, Bradley T. Nat Neurosci Article Experience-induced expression of immediate-early gene Arc/Arg3.1 is known to play a pivotal role in the consolidation of memory. Here we use in-vivo longitudinal multiphoton imaging to show orchestrated activity-dependent expression of Arc in the mouse extrastriate visual cortex in response to a structured visual stimulation. In wild-type mice, the amplitude of the Arc response in individual neurons strongly predicts the probability of reactivation by a subsequent presentation of the same stimulus. In a mouse model of Alzheimer’s disease, this association is markedly disrupted in the cortex specifically near senile plaques. Neurons in the vicinity of plaques are less likely to respond but, paradoxically, there is stronger response in those few neurons around plaques that do respond. To the extent that the orchestrated pattern of Arc expression reflects nervous system responses to, and physiological consolidation of, behavioral experience, the disruption in Arc patterns reveals plaque-associated interference with neural network integration. 2012-08-26 2012-10 /pmc/articles/PMC3458168/ /pubmed/22922786 http://dx.doi.org/10.1038/nn.3199 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Rudinskiy, Nikita
Hawkes, Jonathan M.
Betensky, Rebecca A.
Eguchi, Megumi
Yamaguchi, Shun
Spires-Jones, Tara L.
Hyman, Bradley T.
Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease
title Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease
title_full Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease
title_fullStr Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease
title_full_unstemmed Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease
title_short Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease
title_sort orchestrated experience-driven arc/arg3.1 responses are disrupted in a mouse model of alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458168/
https://www.ncbi.nlm.nih.gov/pubmed/22922786
http://dx.doi.org/10.1038/nn.3199
work_keys_str_mv AT rudinskiynikita orchestratedexperiencedrivenarcarg31responsesaredisruptedinamousemodelofalzheimersdisease
AT hawkesjonathanm orchestratedexperiencedrivenarcarg31responsesaredisruptedinamousemodelofalzheimersdisease
AT betenskyrebeccaa orchestratedexperiencedrivenarcarg31responsesaredisruptedinamousemodelofalzheimersdisease
AT eguchimegumi orchestratedexperiencedrivenarcarg31responsesaredisruptedinamousemodelofalzheimersdisease
AT yamaguchishun orchestratedexperiencedrivenarcarg31responsesaredisruptedinamousemodelofalzheimersdisease
AT spiresjonestaral orchestratedexperiencedrivenarcarg31responsesaredisruptedinamousemodelofalzheimersdisease
AT hymanbradleyt orchestratedexperiencedrivenarcarg31responsesaredisruptedinamousemodelofalzheimersdisease