Cargando…

Molecular Mechanisms of Environmental Enrichment: Impairments in Akt/GSK3β, Neurotrophin-3 and CREB Signaling

Experience of mice in a complex environment enhances neurogenesis and synaptic plasticity in the hippocampus of wild type and transgenic mice harboring familial Alzheimer's disease (FAD)-linked APPswe/PS1ΔE9. In FAD mice, this experience also reduces levels of tau hyperphosphorylation and oligo...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Yuan-Shih, Long, Nancy, Pigino, Gustavo, Brady, Scott T., Lazarov, Orly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660250/
https://www.ncbi.nlm.nih.gov/pubmed/23700479
http://dx.doi.org/10.1371/journal.pone.0064460
_version_ 1782270526816780288
author Hu, Yuan-Shih
Long, Nancy
Pigino, Gustavo
Brady, Scott T.
Lazarov, Orly
author_facet Hu, Yuan-Shih
Long, Nancy
Pigino, Gustavo
Brady, Scott T.
Lazarov, Orly
author_sort Hu, Yuan-Shih
collection PubMed
description Experience of mice in a complex environment enhances neurogenesis and synaptic plasticity in the hippocampus of wild type and transgenic mice harboring familial Alzheimer's disease (FAD)-linked APPswe/PS1ΔE9. In FAD mice, this experience also reduces levels of tau hyperphosphorylation and oligomeric β-amyloid. Although environmental enrichment has significant effects on brain plasticity and neuropathology, the molecular mechanisms underlying these effects are unknown. Here we show that environmental enrichment upregulates the Akt pathway, leading to the downregulation of glycogen synthase kinase 3β (GSK3β), in wild type but not FAD mice. Several neurotrophic signaling pathways are activated in the hippocampus of both wild type and FAD mice, including brain derived neurotrophic factor (BDNF) and nerve growth factor (NGF), and this increase is accompanied by the upregulation of the BDNF receptor, tyrosine kinase B (TrkB). Interestingly, neurotrophin-3 (NT-3) is upregulated in the brains of wild type mice but not FAD mice, while insulin growth factor-1 (IGF-1) is upregulated exclusively in the brains of FAD mice. Upregulation of neurotrophins is accompanied by the increase of N-Methyl-D-aspartic acid (NMDA) receptors in the hippocampus following environmental enrichment. Most importantly, we observed a significant increase in levels of cAMP response element- binding (CREB) transcripts in the hippocampus of wild type and FAD mice following environmental enrichment. However, CREB phosphorylation, a critical step for the initiation of learning and memory-required gene transcription, takes place in the hippocampus of wild type but not of FAD mice. These results suggest that experience of wild type mice in a complex environmental upregulates critical signaling that play a major role in learning and memory in the hippocampus. However, in FAD mice, some of these pathways are impaired and cannot be rescued by environmental enrichment.
format Online
Article
Text
id pubmed-3660250
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36602502013-05-22 Molecular Mechanisms of Environmental Enrichment: Impairments in Akt/GSK3β, Neurotrophin-3 and CREB Signaling Hu, Yuan-Shih Long, Nancy Pigino, Gustavo Brady, Scott T. Lazarov, Orly PLoS One Research Article Experience of mice in a complex environment enhances neurogenesis and synaptic plasticity in the hippocampus of wild type and transgenic mice harboring familial Alzheimer's disease (FAD)-linked APPswe/PS1ΔE9. In FAD mice, this experience also reduces levels of tau hyperphosphorylation and oligomeric β-amyloid. Although environmental enrichment has significant effects on brain plasticity and neuropathology, the molecular mechanisms underlying these effects are unknown. Here we show that environmental enrichment upregulates the Akt pathway, leading to the downregulation of glycogen synthase kinase 3β (GSK3β), in wild type but not FAD mice. Several neurotrophic signaling pathways are activated in the hippocampus of both wild type and FAD mice, including brain derived neurotrophic factor (BDNF) and nerve growth factor (NGF), and this increase is accompanied by the upregulation of the BDNF receptor, tyrosine kinase B (TrkB). Interestingly, neurotrophin-3 (NT-3) is upregulated in the brains of wild type mice but not FAD mice, while insulin growth factor-1 (IGF-1) is upregulated exclusively in the brains of FAD mice. Upregulation of neurotrophins is accompanied by the increase of N-Methyl-D-aspartic acid (NMDA) receptors in the hippocampus following environmental enrichment. Most importantly, we observed a significant increase in levels of cAMP response element- binding (CREB) transcripts in the hippocampus of wild type and FAD mice following environmental enrichment. However, CREB phosphorylation, a critical step for the initiation of learning and memory-required gene transcription, takes place in the hippocampus of wild type but not of FAD mice. These results suggest that experience of wild type mice in a complex environmental upregulates critical signaling that play a major role in learning and memory in the hippocampus. However, in FAD mice, some of these pathways are impaired and cannot be rescued by environmental enrichment. Public Library of Science 2013-05-21 /pmc/articles/PMC3660250/ /pubmed/23700479 http://dx.doi.org/10.1371/journal.pone.0064460 Text en © 2013 Hu 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
Hu, Yuan-Shih
Long, Nancy
Pigino, Gustavo
Brady, Scott T.
Lazarov, Orly
Molecular Mechanisms of Environmental Enrichment: Impairments in Akt/GSK3β, Neurotrophin-3 and CREB Signaling
title Molecular Mechanisms of Environmental Enrichment: Impairments in Akt/GSK3β, Neurotrophin-3 and CREB Signaling
title_full Molecular Mechanisms of Environmental Enrichment: Impairments in Akt/GSK3β, Neurotrophin-3 and CREB Signaling
title_fullStr Molecular Mechanisms of Environmental Enrichment: Impairments in Akt/GSK3β, Neurotrophin-3 and CREB Signaling
title_full_unstemmed Molecular Mechanisms of Environmental Enrichment: Impairments in Akt/GSK3β, Neurotrophin-3 and CREB Signaling
title_short Molecular Mechanisms of Environmental Enrichment: Impairments in Akt/GSK3β, Neurotrophin-3 and CREB Signaling
title_sort molecular mechanisms of environmental enrichment: impairments in akt/gsk3β, neurotrophin-3 and creb signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660250/
https://www.ncbi.nlm.nih.gov/pubmed/23700479
http://dx.doi.org/10.1371/journal.pone.0064460
work_keys_str_mv AT huyuanshih molecularmechanismsofenvironmentalenrichmentimpairmentsinaktgsk3bneurotrophin3andcrebsignaling
AT longnancy molecularmechanismsofenvironmentalenrichmentimpairmentsinaktgsk3bneurotrophin3andcrebsignaling
AT piginogustavo molecularmechanismsofenvironmentalenrichmentimpairmentsinaktgsk3bneurotrophin3andcrebsignaling
AT bradyscottt molecularmechanismsofenvironmentalenrichmentimpairmentsinaktgsk3bneurotrophin3andcrebsignaling
AT lazarovorly molecularmechanismsofenvironmentalenrichmentimpairmentsinaktgsk3bneurotrophin3andcrebsignaling