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Neural maturation enhanced by exercise-induced extracellular derivatives

Physical activity has profound effects on neuronal progenitor cell growth, differentiation, and integration, but the mechanism for these effects is still ambiguous. Using a mouse model, we investigated the effects of two weeks of treadmill running on the dynamics of the size distribution and miRNA p...

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Autores principales: Moon, Hyo Youl, Yoon, Kyeong Jin, Lee, Won Sang, Cho, Hae-Sung, Kim, Do-Yeon, Kim, Ji-Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054262/
https://www.ncbi.nlm.nih.gov/pubmed/32127592
http://dx.doi.org/10.1038/s41598-020-60930-6
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author Moon, Hyo Youl
Yoon, Kyeong Jin
Lee, Won Sang
Cho, Hae-Sung
Kim, Do-Yeon
Kim, Ji-Seok
author_facet Moon, Hyo Youl
Yoon, Kyeong Jin
Lee, Won Sang
Cho, Hae-Sung
Kim, Do-Yeon
Kim, Ji-Seok
author_sort Moon, Hyo Youl
collection PubMed
description Physical activity has profound effects on neuronal progenitor cell growth, differentiation, and integration, but the mechanism for these effects is still ambiguous. Using a mouse model, we investigated the effects of two weeks of treadmill running on the dynamics of the size distribution and miRNA profiles of serum extracellular derivatives (EDs) using particle-sizing analysis and small RNA sequencing. We found that an increased average diameter of EDs in the running group compared with the sedentary group (p < 0.05), and 16 miRNAs were significantly altered (p < 0.05) in the running group. Furthermore, functional annotation analysis of differentially expressed miRNA-predicted target genes showed that many of these target genes are involved in the PI3K-Akt pathway. Exercise-induced serum EDs increased Neuro2A cell viability and Akt phosphorylation. We also found that expression levels of neuronal maturation markers such as Microtubule-Associated Protein 2 (MAP2ab) and Neuronal nuclei (NeuN) were increased (p < 0.05, respectively), and that inhibition of the PI3K-Akt pathway by LY294002 pre-treatment ameliorated their expression in Neuro2A cells. Finally, the administration of exercise-induced EDs for 3 days increased the Histone 3 phosphorylation and β-III tubulin expression in Ink/Arf null neural stem cells and progenitors (NSPCs) under each proliferation and differentiation condition. These results suggest that exercise-induced circulating EDs may mediate neuronal maturation during exercise.
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spelling pubmed-70542622020-03-11 Neural maturation enhanced by exercise-induced extracellular derivatives Moon, Hyo Youl Yoon, Kyeong Jin Lee, Won Sang Cho, Hae-Sung Kim, Do-Yeon Kim, Ji-Seok Sci Rep Article Physical activity has profound effects on neuronal progenitor cell growth, differentiation, and integration, but the mechanism for these effects is still ambiguous. Using a mouse model, we investigated the effects of two weeks of treadmill running on the dynamics of the size distribution and miRNA profiles of serum extracellular derivatives (EDs) using particle-sizing analysis and small RNA sequencing. We found that an increased average diameter of EDs in the running group compared with the sedentary group (p < 0.05), and 16 miRNAs were significantly altered (p < 0.05) in the running group. Furthermore, functional annotation analysis of differentially expressed miRNA-predicted target genes showed that many of these target genes are involved in the PI3K-Akt pathway. Exercise-induced serum EDs increased Neuro2A cell viability and Akt phosphorylation. We also found that expression levels of neuronal maturation markers such as Microtubule-Associated Protein 2 (MAP2ab) and Neuronal nuclei (NeuN) were increased (p < 0.05, respectively), and that inhibition of the PI3K-Akt pathway by LY294002 pre-treatment ameliorated their expression in Neuro2A cells. Finally, the administration of exercise-induced EDs for 3 days increased the Histone 3 phosphorylation and β-III tubulin expression in Ink/Arf null neural stem cells and progenitors (NSPCs) under each proliferation and differentiation condition. These results suggest that exercise-induced circulating EDs may mediate neuronal maturation during exercise. Nature Publishing Group UK 2020-03-03 /pmc/articles/PMC7054262/ /pubmed/32127592 http://dx.doi.org/10.1038/s41598-020-60930-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Moon, Hyo Youl
Yoon, Kyeong Jin
Lee, Won Sang
Cho, Hae-Sung
Kim, Do-Yeon
Kim, Ji-Seok
Neural maturation enhanced by exercise-induced extracellular derivatives
title Neural maturation enhanced by exercise-induced extracellular derivatives
title_full Neural maturation enhanced by exercise-induced extracellular derivatives
title_fullStr Neural maturation enhanced by exercise-induced extracellular derivatives
title_full_unstemmed Neural maturation enhanced by exercise-induced extracellular derivatives
title_short Neural maturation enhanced by exercise-induced extracellular derivatives
title_sort neural maturation enhanced by exercise-induced extracellular derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054262/
https://www.ncbi.nlm.nih.gov/pubmed/32127592
http://dx.doi.org/10.1038/s41598-020-60930-6
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