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Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex
Aerobic exercise (AE) is known to produce beneficial effects on brain health by improving plasticity, connectivity, and cognitive functions, but the underlying molecular mechanisms are still limited. Neurexins (Nrxns) are a family of presynaptic cell adhesion molecules that are important in synapsis...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261640/ https://www.ncbi.nlm.nih.gov/pubmed/34072692 http://dx.doi.org/10.3390/jfmk6020048 |
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author | Innocenzi, Elisa Cariati, Ida De Domenico, Emanuela Tiberi, Erika D’Arcangelo, Giovanna Verdile, Veronica Paronetto, Maria Paola Tancredi, Virginia Barchi, Marco Rossi, Pellegrino Sette, Claudio Grimaldi, Paola |
author_facet | Innocenzi, Elisa Cariati, Ida De Domenico, Emanuela Tiberi, Erika D’Arcangelo, Giovanna Verdile, Veronica Paronetto, Maria Paola Tancredi, Virginia Barchi, Marco Rossi, Pellegrino Sette, Claudio Grimaldi, Paola |
author_sort | Innocenzi, Elisa |
collection | PubMed |
description | Aerobic exercise (AE) is known to produce beneficial effects on brain health by improving plasticity, connectivity, and cognitive functions, but the underlying molecular mechanisms are still limited. Neurexins (Nrxns) are a family of presynaptic cell adhesion molecules that are important in synapsis formation and maturation. In vertebrates, three-neurexin genes (NRXN1, NRXN2, and NRXN3) have been identified, each encoding for α and β neurexins, from two independent promoters. Moreover, each Nrxns gene (1–3) has several alternative exons and produces many splice variants that bind to a large variety of postsynaptic ligands, playing a role in trans-synaptic specification, strength, and plasticity. In this study, we investigated the impact of a continuous progressive (CP) AE program on alternative splicing (AS) of Nrxns on two brain regions: frontal cortex (FC) and hippocampus. We showed that exercise promoted Nrxns1–3 AS at splice site 4 (SS4) both in α and β isoforms, inducing a switch from exon-excluded isoforms (SS4−) to exon-included isoforms (SS4+) in FC but not in hippocampus. Additionally, we showed that the same AE program enhanced the expression level of other genes correlated with synaptic function and plasticity only in FC. Altogether, our findings demonstrated the positive effect of CP AE on FC in inducing molecular changes underlying synaptic plasticity and suggested that FC is possibly a more sensitive structure than hippocampus to show molecular changes. |
format | Online Article Text |
id | pubmed-8261640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82616402021-07-21 Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex Innocenzi, Elisa Cariati, Ida De Domenico, Emanuela Tiberi, Erika D’Arcangelo, Giovanna Verdile, Veronica Paronetto, Maria Paola Tancredi, Virginia Barchi, Marco Rossi, Pellegrino Sette, Claudio Grimaldi, Paola J Funct Morphol Kinesiol Communication Aerobic exercise (AE) is known to produce beneficial effects on brain health by improving plasticity, connectivity, and cognitive functions, but the underlying molecular mechanisms are still limited. Neurexins (Nrxns) are a family of presynaptic cell adhesion molecules that are important in synapsis formation and maturation. In vertebrates, three-neurexin genes (NRXN1, NRXN2, and NRXN3) have been identified, each encoding for α and β neurexins, from two independent promoters. Moreover, each Nrxns gene (1–3) has several alternative exons and produces many splice variants that bind to a large variety of postsynaptic ligands, playing a role in trans-synaptic specification, strength, and plasticity. In this study, we investigated the impact of a continuous progressive (CP) AE program on alternative splicing (AS) of Nrxns on two brain regions: frontal cortex (FC) and hippocampus. We showed that exercise promoted Nrxns1–3 AS at splice site 4 (SS4) both in α and β isoforms, inducing a switch from exon-excluded isoforms (SS4−) to exon-included isoforms (SS4+) in FC but not in hippocampus. Additionally, we showed that the same AE program enhanced the expression level of other genes correlated with synaptic function and plasticity only in FC. Altogether, our findings demonstrated the positive effect of CP AE on FC in inducing molecular changes underlying synaptic plasticity and suggested that FC is possibly a more sensitive structure than hippocampus to show molecular changes. MDPI 2021-05-31 /pmc/articles/PMC8261640/ /pubmed/34072692 http://dx.doi.org/10.3390/jfmk6020048 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Innocenzi, Elisa Cariati, Ida De Domenico, Emanuela Tiberi, Erika D’Arcangelo, Giovanna Verdile, Veronica Paronetto, Maria Paola Tancredi, Virginia Barchi, Marco Rossi, Pellegrino Sette, Claudio Grimaldi, Paola Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex |
title | Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex |
title_full | Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex |
title_fullStr | Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex |
title_full_unstemmed | Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex |
title_short | Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex |
title_sort | aerobic exercise induces alternative splicing of neurexins in frontal cortex |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261640/ https://www.ncbi.nlm.nih.gov/pubmed/34072692 http://dx.doi.org/10.3390/jfmk6020048 |
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