Cargando…

Physical Activity and Post-Transcriptional Regulation of Aging Decay: Modulation of Pathways in Postmenopausal Osteoporosis

Background and Objectives: Bones and the skeletal muscle play a key role in human physiology as regulators of metabolism in the whole organism. Bone tissue is identified as a complex and dynamic living unit that could react to physical activity. Hormones, growth factors, signaling factors, and envir...

Descripción completa

Detalles Bibliográficos
Autores principales: Vita, Federica, Gangemi, Sebastiano, Pioggia, Giovanni, Trimarchi, Fabio, Di Mauro, Debora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228623/
https://www.ncbi.nlm.nih.gov/pubmed/35744030
http://dx.doi.org/10.3390/medicina58060767
_version_ 1784734525484433408
author Vita, Federica
Gangemi, Sebastiano
Pioggia, Giovanni
Trimarchi, Fabio
Di Mauro, Debora
author_facet Vita, Federica
Gangemi, Sebastiano
Pioggia, Giovanni
Trimarchi, Fabio
Di Mauro, Debora
author_sort Vita, Federica
collection PubMed
description Background and Objectives: Bones and the skeletal muscle play a key role in human physiology as regulators of metabolism in the whole organism. Bone tissue is identified as a complex and dynamic living unit that could react to physical activity. Hormones, growth factors, signaling factors, and environmental factors control osteogenesis, and it could be regulated at a post-transcriptional level. MicroRNAs (miRNAs) can interfere with mRNAs translation. Increasing data suggest that miRNAs, through different pathways, are involved in the regulation of bone marrow mesenchymal stem cells (BMSCs) differentiation and physical activity-induced bone remodeling. The purpose of this narrative review is to investigate the potential protective role played by physical activity in affecting miRNAs expression in close tissues and elaborate on the complex network of interplay that could drive various metabolic responses of the bone to physical activity. Materials and Methods: A bibliographic search of the scientific literature was carried out in scientific databases to investigate the possible effect of physical activity on age-related features detected in the musculoskeletal system. Results: Several studies suggested that the musculoskeletal system interacting at a biomolecular level could establish crosstalk between bone and muscle in an endocrine or paracrine way through myokines released by muscle at the periosteal interface or in the bloodstream, such as irisin. Mechanical stimuli have a key role in bone formation and resorption, increasing osteogenesis and downregulating adipogenesis of BMSC via regulation of expression of runt-related transcription factor 2 (Runx2) and peroxisome proliferator-activated receptor gamma (PPARγ), respectively. Conclusions: Increasing data suggest that miRNAs, through different pathways, are involved in the regulation of BMSCs differentiation and physical activity-induced bone remodeling. Modulation of miRNAs following physical exercise represents an interesting field of investigation since these non-coding RNAs may be considered defenders against degenerative diseases and as well as useful prognostic markers in skeletal and muscle-skeletal diseases, such as osteoporosis.
format Online
Article
Text
id pubmed-9228623
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-92286232022-06-25 Physical Activity and Post-Transcriptional Regulation of Aging Decay: Modulation of Pathways in Postmenopausal Osteoporosis Vita, Federica Gangemi, Sebastiano Pioggia, Giovanni Trimarchi, Fabio Di Mauro, Debora Medicina (Kaunas) Review Background and Objectives: Bones and the skeletal muscle play a key role in human physiology as regulators of metabolism in the whole organism. Bone tissue is identified as a complex and dynamic living unit that could react to physical activity. Hormones, growth factors, signaling factors, and environmental factors control osteogenesis, and it could be regulated at a post-transcriptional level. MicroRNAs (miRNAs) can interfere with mRNAs translation. Increasing data suggest that miRNAs, through different pathways, are involved in the regulation of bone marrow mesenchymal stem cells (BMSCs) differentiation and physical activity-induced bone remodeling. The purpose of this narrative review is to investigate the potential protective role played by physical activity in affecting miRNAs expression in close tissues and elaborate on the complex network of interplay that could drive various metabolic responses of the bone to physical activity. Materials and Methods: A bibliographic search of the scientific literature was carried out in scientific databases to investigate the possible effect of physical activity on age-related features detected in the musculoskeletal system. Results: Several studies suggested that the musculoskeletal system interacting at a biomolecular level could establish crosstalk between bone and muscle in an endocrine or paracrine way through myokines released by muscle at the periosteal interface or in the bloodstream, such as irisin. Mechanical stimuli have a key role in bone formation and resorption, increasing osteogenesis and downregulating adipogenesis of BMSC via regulation of expression of runt-related transcription factor 2 (Runx2) and peroxisome proliferator-activated receptor gamma (PPARγ), respectively. Conclusions: Increasing data suggest that miRNAs, through different pathways, are involved in the regulation of BMSCs differentiation and physical activity-induced bone remodeling. Modulation of miRNAs following physical exercise represents an interesting field of investigation since these non-coding RNAs may be considered defenders against degenerative diseases and as well as useful prognostic markers in skeletal and muscle-skeletal diseases, such as osteoporosis. MDPI 2022-06-06 /pmc/articles/PMC9228623/ /pubmed/35744030 http://dx.doi.org/10.3390/medicina58060767 Text en © 2022 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 Review
Vita, Federica
Gangemi, Sebastiano
Pioggia, Giovanni
Trimarchi, Fabio
Di Mauro, Debora
Physical Activity and Post-Transcriptional Regulation of Aging Decay: Modulation of Pathways in Postmenopausal Osteoporosis
title Physical Activity and Post-Transcriptional Regulation of Aging Decay: Modulation of Pathways in Postmenopausal Osteoporosis
title_full Physical Activity and Post-Transcriptional Regulation of Aging Decay: Modulation of Pathways in Postmenopausal Osteoporosis
title_fullStr Physical Activity and Post-Transcriptional Regulation of Aging Decay: Modulation of Pathways in Postmenopausal Osteoporosis
title_full_unstemmed Physical Activity and Post-Transcriptional Regulation of Aging Decay: Modulation of Pathways in Postmenopausal Osteoporosis
title_short Physical Activity and Post-Transcriptional Regulation of Aging Decay: Modulation of Pathways in Postmenopausal Osteoporosis
title_sort physical activity and post-transcriptional regulation of aging decay: modulation of pathways in postmenopausal osteoporosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228623/
https://www.ncbi.nlm.nih.gov/pubmed/35744030
http://dx.doi.org/10.3390/medicina58060767
work_keys_str_mv AT vitafederica physicalactivityandposttranscriptionalregulationofagingdecaymodulationofpathwaysinpostmenopausalosteoporosis
AT gangemisebastiano physicalactivityandposttranscriptionalregulationofagingdecaymodulationofpathwaysinpostmenopausalosteoporosis
AT pioggiagiovanni physicalactivityandposttranscriptionalregulationofagingdecaymodulationofpathwaysinpostmenopausalosteoporosis
AT trimarchifabio physicalactivityandposttranscriptionalregulationofagingdecaymodulationofpathwaysinpostmenopausalosteoporosis
AT dimaurodebora physicalactivityandposttranscriptionalregulationofagingdecaymodulationofpathwaysinpostmenopausalosteoporosis