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Cortical gene transcription response patterns to water maze training in aged mice

BACKGROUND: The hippocampus mediates the acquisition of spatial memory, but the memory trace is eventually transferred to the cortex. We have investigated transcriptional activation of pathways related to cognitive function in the cortex of the aged mouse by analyzing gene expression following water...

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Autores principales: Park, Sung-Soo, Stranahan, Alexis M, Chadwick, Wayne, Zhou, Yu, Wang, Liyun, Martin, Bronwen, Becker, Kevin G, Maudsley, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142531/
https://www.ncbi.nlm.nih.gov/pubmed/21714909
http://dx.doi.org/10.1186/1471-2202-12-63
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author Park, Sung-Soo
Stranahan, Alexis M
Chadwick, Wayne
Zhou, Yu
Wang, Liyun
Martin, Bronwen
Becker, Kevin G
Maudsley, Stuart
author_facet Park, Sung-Soo
Stranahan, Alexis M
Chadwick, Wayne
Zhou, Yu
Wang, Liyun
Martin, Bronwen
Becker, Kevin G
Maudsley, Stuart
author_sort Park, Sung-Soo
collection PubMed
description BACKGROUND: The hippocampus mediates the acquisition of spatial memory, but the memory trace is eventually transferred to the cortex. We have investigated transcriptional activation of pathways related to cognitive function in the cortex of the aged mouse by analyzing gene expression following water maze training. RESULTS: We identified genes that were differentially responsive in aged mice with accurate spatial performance during probe trials or repeated swimming sessions, relative to home cage conditions. Effective learners exhibited significantly greater activation of several pathways, such as the mitogen-activated protein kinase and insulin receptor signaling pathways, relative to swimmers. The genes encoding activity-related cytoskeletal protein (Arc) and brain-derived neurotrophic factor (BDNF) were upregulated in proficient learners, relative to swimmers and home cage controls, while the gene encoding Rho GTPase activating protein 32 (GRIT) was downregulated. We explored the regulation of Arc, BDNF, and GRIT expression in greater morphological detail using in situ hybridization. Recall during probe trials enhanced Arc expression across multiple cortical regions involved in the cognitive component of water maze learning, while BDNF expression was more homogeneously upregulated across cortical regions involved in the associational and sensorimotor aspects of water maze training. In contrast, levels of GRIT expression were uniformly reduced across all cortical regions examined. CONCLUSIONS: These results suggest that cortical gene transcription is responsive to learning in aged mice that exhibit behavioral proficiency, and support a distributed hypothesis of memory storage across multiple cortical compartments.
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spelling pubmed-31425312011-07-24 Cortical gene transcription response patterns to water maze training in aged mice Park, Sung-Soo Stranahan, Alexis M Chadwick, Wayne Zhou, Yu Wang, Liyun Martin, Bronwen Becker, Kevin G Maudsley, Stuart BMC Neurosci Research Article BACKGROUND: The hippocampus mediates the acquisition of spatial memory, but the memory trace is eventually transferred to the cortex. We have investigated transcriptional activation of pathways related to cognitive function in the cortex of the aged mouse by analyzing gene expression following water maze training. RESULTS: We identified genes that were differentially responsive in aged mice with accurate spatial performance during probe trials or repeated swimming sessions, relative to home cage conditions. Effective learners exhibited significantly greater activation of several pathways, such as the mitogen-activated protein kinase and insulin receptor signaling pathways, relative to swimmers. The genes encoding activity-related cytoskeletal protein (Arc) and brain-derived neurotrophic factor (BDNF) were upregulated in proficient learners, relative to swimmers and home cage controls, while the gene encoding Rho GTPase activating protein 32 (GRIT) was downregulated. We explored the regulation of Arc, BDNF, and GRIT expression in greater morphological detail using in situ hybridization. Recall during probe trials enhanced Arc expression across multiple cortical regions involved in the cognitive component of water maze learning, while BDNF expression was more homogeneously upregulated across cortical regions involved in the associational and sensorimotor aspects of water maze training. In contrast, levels of GRIT expression were uniformly reduced across all cortical regions examined. CONCLUSIONS: These results suggest that cortical gene transcription is responsive to learning in aged mice that exhibit behavioral proficiency, and support a distributed hypothesis of memory storage across multiple cortical compartments. BioMed Central 2011-06-29 /pmc/articles/PMC3142531/ /pubmed/21714909 http://dx.doi.org/10.1186/1471-2202-12-63 Text en Copyright ©2011 Park et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Park, Sung-Soo
Stranahan, Alexis M
Chadwick, Wayne
Zhou, Yu
Wang, Liyun
Martin, Bronwen
Becker, Kevin G
Maudsley, Stuart
Cortical gene transcription response patterns to water maze training in aged mice
title Cortical gene transcription response patterns to water maze training in aged mice
title_full Cortical gene transcription response patterns to water maze training in aged mice
title_fullStr Cortical gene transcription response patterns to water maze training in aged mice
title_full_unstemmed Cortical gene transcription response patterns to water maze training in aged mice
title_short Cortical gene transcription response patterns to water maze training in aged mice
title_sort cortical gene transcription response patterns to water maze training in aged mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142531/
https://www.ncbi.nlm.nih.gov/pubmed/21714909
http://dx.doi.org/10.1186/1471-2202-12-63
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