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Experience Recruits MSK1 to Expand the Dynamic Range of Synapses and Enhance Cognition

Experience powerfully influences neuronal function and cognitive performance, but the cellular and molecular events underlying the experience-dependent enhancement of mental ability have remained elusive. In particular, the mechanisms that couple the external environment to the genomic changes under...

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Autores principales: Privitera, Lucia, Morè, Lorenzo, Cooper, Daniel D., Richardson, Philippa, Tsogka, Marianthi, Hebenstreit, Daniel, Arthur, J. Simon C., Frenguelli, Bruno G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294801/
https://www.ncbi.nlm.nih.gov/pubmed/32376781
http://dx.doi.org/10.1523/JNEUROSCI.2765-19.2020
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author Privitera, Lucia
Morè, Lorenzo
Cooper, Daniel D.
Richardson, Philippa
Tsogka, Marianthi
Hebenstreit, Daniel
Arthur, J. Simon C.
Frenguelli, Bruno G.
author_facet Privitera, Lucia
Morè, Lorenzo
Cooper, Daniel D.
Richardson, Philippa
Tsogka, Marianthi
Hebenstreit, Daniel
Arthur, J. Simon C.
Frenguelli, Bruno G.
author_sort Privitera, Lucia
collection PubMed
description Experience powerfully influences neuronal function and cognitive performance, but the cellular and molecular events underlying the experience-dependent enhancement of mental ability have remained elusive. In particular, the mechanisms that couple the external environment to the genomic changes underpinning this improvement are unknown. To address this, we have used male mice harboring an inactivating mutation of mitogen- and stress-activated protein kinase 1 (MSK1), a brain-derived neurotrophic factor (BDNF)-activated enzyme downstream of the mitogen-activated protein kinase (MAPK) pathway. We show that MSK1 is required for the full extent of experience-induced improvement of spatial memory, for the expansion of the dynamic range of synapses, exemplified by the enhancement of hippocampal long-term potentiation (LTP) and long-term depression (LTD), and for the regulation of the majority of genes influenced by enrichment. In addition, and unexpectedly, we show that experience is associated with an MSK1-dependent downregulation of key MAPK and plasticity-related genes, notably of EGR1/Zif268 and Arc/Arg3.1, suggesting the establishment of a novel genomic landscape adapted to experience. By coupling experience to homeostatic changes in gene expression MSK1, represents a prime mechanism through which the external environment has an enduring influence on gene expression, synaptic function, and cognition. SIGNIFICANCE STATEMENT Our everyday experiences strongly influence the structure and function of the brain. Positive experiences encourage the growth and development of the brain and support enhanced learning and memory and resistance to mood disorders such as anxiety. While this has been known for many years, how this occurs is not clear. Here, we show that many of the positive aspects of experience depend on an enzyme called mitogen- and stress-activated protein kinase 1 (MSK1). Using male mice with a mutation in MSK1, we show that MSK1 is necessary for the majority of gene expression changes associated with experience, extending the range over which the communication between neurons occurs, and for both the persistence of memory and the ability to learn new task rules.
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spelling pubmed-72948012020-06-15 Experience Recruits MSK1 to Expand the Dynamic Range of Synapses and Enhance Cognition Privitera, Lucia Morè, Lorenzo Cooper, Daniel D. Richardson, Philippa Tsogka, Marianthi Hebenstreit, Daniel Arthur, J. Simon C. Frenguelli, Bruno G. J Neurosci Research Articles Experience powerfully influences neuronal function and cognitive performance, but the cellular and molecular events underlying the experience-dependent enhancement of mental ability have remained elusive. In particular, the mechanisms that couple the external environment to the genomic changes underpinning this improvement are unknown. To address this, we have used male mice harboring an inactivating mutation of mitogen- and stress-activated protein kinase 1 (MSK1), a brain-derived neurotrophic factor (BDNF)-activated enzyme downstream of the mitogen-activated protein kinase (MAPK) pathway. We show that MSK1 is required for the full extent of experience-induced improvement of spatial memory, for the expansion of the dynamic range of synapses, exemplified by the enhancement of hippocampal long-term potentiation (LTP) and long-term depression (LTD), and for the regulation of the majority of genes influenced by enrichment. In addition, and unexpectedly, we show that experience is associated with an MSK1-dependent downregulation of key MAPK and plasticity-related genes, notably of EGR1/Zif268 and Arc/Arg3.1, suggesting the establishment of a novel genomic landscape adapted to experience. By coupling experience to homeostatic changes in gene expression MSK1, represents a prime mechanism through which the external environment has an enduring influence on gene expression, synaptic function, and cognition. SIGNIFICANCE STATEMENT Our everyday experiences strongly influence the structure and function of the brain. Positive experiences encourage the growth and development of the brain and support enhanced learning and memory and resistance to mood disorders such as anxiety. While this has been known for many years, how this occurs is not clear. Here, we show that many of the positive aspects of experience depend on an enzyme called mitogen- and stress-activated protein kinase 1 (MSK1). Using male mice with a mutation in MSK1, we show that MSK1 is necessary for the majority of gene expression changes associated with experience, extending the range over which the communication between neurons occurs, and for both the persistence of memory and the ability to learn new task rules. Society for Neuroscience 2020-06-10 /pmc/articles/PMC7294801/ /pubmed/32376781 http://dx.doi.org/10.1523/JNEUROSCI.2765-19.2020 Text en Copyright © 2020 Privitera, Morè et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License Creative Commons Attribution 4.0 International (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Privitera, Lucia
Morè, Lorenzo
Cooper, Daniel D.
Richardson, Philippa
Tsogka, Marianthi
Hebenstreit, Daniel
Arthur, J. Simon C.
Frenguelli, Bruno G.
Experience Recruits MSK1 to Expand the Dynamic Range of Synapses and Enhance Cognition
title Experience Recruits MSK1 to Expand the Dynamic Range of Synapses and Enhance Cognition
title_full Experience Recruits MSK1 to Expand the Dynamic Range of Synapses and Enhance Cognition
title_fullStr Experience Recruits MSK1 to Expand the Dynamic Range of Synapses and Enhance Cognition
title_full_unstemmed Experience Recruits MSK1 to Expand the Dynamic Range of Synapses and Enhance Cognition
title_short Experience Recruits MSK1 to Expand the Dynamic Range of Synapses and Enhance Cognition
title_sort experience recruits msk1 to expand the dynamic range of synapses and enhance cognition
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294801/
https://www.ncbi.nlm.nih.gov/pubmed/32376781
http://dx.doi.org/10.1523/JNEUROSCI.2765-19.2020
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