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Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy
Insulin-like growth factor-1 (IGF-1) is a key growth factor that regulates both anabolic and catabolic pathways in skeletal muscle. IGF-1 increases skeletal muscle protein synthesis via PI3K/Akt/mTOR and PI3K/Akt/GSK3β pathways. PI3K/Akt can also inhibit FoxOs and suppress transcription of E3 ubiqui...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564605/ https://www.ncbi.nlm.nih.gov/pubmed/32858949 http://dx.doi.org/10.3390/cells9091970 |
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author | Yoshida, Tadashi Delafontaine, Patrice |
author_facet | Yoshida, Tadashi Delafontaine, Patrice |
author_sort | Yoshida, Tadashi |
collection | PubMed |
description | Insulin-like growth factor-1 (IGF-1) is a key growth factor that regulates both anabolic and catabolic pathways in skeletal muscle. IGF-1 increases skeletal muscle protein synthesis via PI3K/Akt/mTOR and PI3K/Akt/GSK3β pathways. PI3K/Akt can also inhibit FoxOs and suppress transcription of E3 ubiquitin ligases that regulate ubiquitin proteasome system (UPS)-mediated protein degradation. Autophagy is likely inhibited by IGF-1 via mTOR and FoxO signaling, although the contribution of autophagy regulation in IGF-1-mediated inhibition of skeletal muscle atrophy remains to be determined. Evidence has suggested that IGF-1/Akt can inhibit muscle atrophy-inducing cytokine and myostatin signaling via inhibition of the NF-κΒ and Smad pathways, respectively. Several miRNAs have been found to regulate IGF-1 signaling in skeletal muscle, and these miRs are likely regulated in different pathological conditions and contribute to the development of muscle atrophy. IGF-1 also potentiates skeletal muscle regeneration via activation of skeletal muscle stem (satellite) cells, which may contribute to muscle hypertrophy and/or inhibit atrophy. Importantly, IGF-1 levels and IGF-1R downstream signaling are suppressed in many chronic disease conditions and likely result in muscle atrophy via the combined effects of altered protein synthesis, UPS activity, autophagy, and muscle regeneration. |
format | Online Article Text |
id | pubmed-7564605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75646052020-10-29 Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy Yoshida, Tadashi Delafontaine, Patrice Cells Review Insulin-like growth factor-1 (IGF-1) is a key growth factor that regulates both anabolic and catabolic pathways in skeletal muscle. IGF-1 increases skeletal muscle protein synthesis via PI3K/Akt/mTOR and PI3K/Akt/GSK3β pathways. PI3K/Akt can also inhibit FoxOs and suppress transcription of E3 ubiquitin ligases that regulate ubiquitin proteasome system (UPS)-mediated protein degradation. Autophagy is likely inhibited by IGF-1 via mTOR and FoxO signaling, although the contribution of autophagy regulation in IGF-1-mediated inhibition of skeletal muscle atrophy remains to be determined. Evidence has suggested that IGF-1/Akt can inhibit muscle atrophy-inducing cytokine and myostatin signaling via inhibition of the NF-κΒ and Smad pathways, respectively. Several miRNAs have been found to regulate IGF-1 signaling in skeletal muscle, and these miRs are likely regulated in different pathological conditions and contribute to the development of muscle atrophy. IGF-1 also potentiates skeletal muscle regeneration via activation of skeletal muscle stem (satellite) cells, which may contribute to muscle hypertrophy and/or inhibit atrophy. Importantly, IGF-1 levels and IGF-1R downstream signaling are suppressed in many chronic disease conditions and likely result in muscle atrophy via the combined effects of altered protein synthesis, UPS activity, autophagy, and muscle regeneration. MDPI 2020-08-26 /pmc/articles/PMC7564605/ /pubmed/32858949 http://dx.doi.org/10.3390/cells9091970 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Yoshida, Tadashi Delafontaine, Patrice Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy |
title | Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy |
title_full | Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy |
title_fullStr | Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy |
title_full_unstemmed | Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy |
title_short | Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy |
title_sort | mechanisms of igf-1-mediated regulation of skeletal muscle hypertrophy and atrophy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564605/ https://www.ncbi.nlm.nih.gov/pubmed/32858949 http://dx.doi.org/10.3390/cells9091970 |
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