Does the blunted stimulation of skeletal muscle protein synthesis by aging in response to mechanical load result from impaired ribosome biogenesis?

IF 3.3 Q2 GERIATRICS & GERONTOLOGY Frontiers in aging Pub Date : 2023-01-01 DOI:10.3389/fragi.2023.1171850
Thomas Chaillou, Diego Montiel-Rojas
{"title":"Does the blunted stimulation of skeletal muscle protein synthesis by aging in response to mechanical load result from impaired ribosome biogenesis?","authors":"Thomas Chaillou,&nbsp;Diego Montiel-Rojas","doi":"10.3389/fragi.2023.1171850","DOIUrl":null,"url":null,"abstract":"<p><p>Age-related loss of skeletal muscle mass leads to a reduction of strength. It is likely due to an inadequate stimulation of muscle protein synthesis (MPS) in response to anabolic stimuli, such as mechanical load. Ribosome biogenesis is a major determinant of translational capacity and is essential for the control of muscle mass. This mini-review aims to put forth the hypothesis that ribosome biogenesis is impaired by aging in response to mechanical load, which could contribute to the age-related anabolic resistance and progressive muscle atrophy. Recent animal studies indicate that aging impedes muscle hypertrophic response to mechanical overload. This is associated with an impaired transcription of ribosomal DNA (rDNA) by RNA polymerase I (Pol I), a limited increase in total RNA concentration, a blunted activation of AKT/mTOR pathway, and an increased phosphorylation of AMPK. In contrast, an age-mediated impairment of ribosome biogenesis is unlikely in response to electrical stimulations. In human, the hypertrophic response to resistance exercise training is diminished with age. This is accompanied by a deficit in long-term MPS and an absence of increased total RNA concentration. The results addressing the acute response to resistance exercise suggest an impaired Pol I-mediated rDNA transcription and attenuated activation/expression of several upstream regulators of ribosome biogenesis in muscles from aged individuals. Altogether, emerging evidence indicates that impaired ribosome biogenesis could partly explain age-related anabolic resistance to mechanical load, which may ultimately contribute to progressive muscle atrophy. Future research should develop more advanced molecular tools to provide in-depth analysis of muscle ribosome biogenesis.</p>","PeriodicalId":73061,"journal":{"name":"Frontiers in aging","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225510/pdf/","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in aging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fragi.2023.1171850","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Age-related loss of skeletal muscle mass leads to a reduction of strength. It is likely due to an inadequate stimulation of muscle protein synthesis (MPS) in response to anabolic stimuli, such as mechanical load. Ribosome biogenesis is a major determinant of translational capacity and is essential for the control of muscle mass. This mini-review aims to put forth the hypothesis that ribosome biogenesis is impaired by aging in response to mechanical load, which could contribute to the age-related anabolic resistance and progressive muscle atrophy. Recent animal studies indicate that aging impedes muscle hypertrophic response to mechanical overload. This is associated with an impaired transcription of ribosomal DNA (rDNA) by RNA polymerase I (Pol I), a limited increase in total RNA concentration, a blunted activation of AKT/mTOR pathway, and an increased phosphorylation of AMPK. In contrast, an age-mediated impairment of ribosome biogenesis is unlikely in response to electrical stimulations. In human, the hypertrophic response to resistance exercise training is diminished with age. This is accompanied by a deficit in long-term MPS and an absence of increased total RNA concentration. The results addressing the acute response to resistance exercise suggest an impaired Pol I-mediated rDNA transcription and attenuated activation/expression of several upstream regulators of ribosome biogenesis in muscles from aged individuals. Altogether, emerging evidence indicates that impaired ribosome biogenesis could partly explain age-related anabolic resistance to mechanical load, which may ultimately contribute to progressive muscle atrophy. Future research should develop more advanced molecular tools to provide in-depth analysis of muscle ribosome biogenesis.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
老化对骨骼肌蛋白质合成的钝化刺激是对机械负荷的反应,是核糖体生物发生受损的结果吗?
与年龄相关的骨骼肌质量损失导致力量下降。这可能是由于肌肉蛋白质合成(MPS)在响应合成代谢刺激(如机械负荷)时刺激不足所致。核糖体的生物发生是翻译能力的主要决定因素,对肌肉质量的控制至关重要。这篇综述旨在提出核糖体生物发生因机械负荷的老化而受损的假设,这可能导致与年龄相关的合成代谢抵抗和进行性肌肉萎缩。最近的动物研究表明,衰老会阻碍肌肉对机械负荷的肥厚反应。这与RNA聚合酶I (Pol I)对核糖体DNA (rDNA)的转录受损、总RNA浓度的有限增加、AKT/mTOR通路的激活减弱以及AMPK磷酸化增加有关。相反,年龄介导的核糖体生物发生损伤不太可能是对电刺激的反应。在人类中,抗阻运动训练的肥厚反应随着年龄的增长而减弱。这伴随着长期MPS的缺陷和总RNA浓度增加的缺失。研究结果表明,老年人肌肉中Pol i介导的rDNA转录受损,核糖体生物发生的几个上游调节因子的激活/表达减弱。总之,新出现的证据表明,核糖体生物发生受损可以部分解释与年龄相关的合成代谢抵抗机械负荷,这可能最终导致进行性肌肉萎缩。未来的研究应开发更先进的分子工具来深入分析肌肉核糖体的生物发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
3.00
自引率
0.00%
发文量
0
审稿时长
13 weeks
期刊最新文献
The role of high mobility group proteins in cellular senescence mechanisms. Impact of hearing rehabilitation programs on presbycusis management: a systematic review and meta-analysis of randomized controlled trials. Can salivary and skin microbiome become a biodetector for aging-associated diseases? Current insights and future perspectives. Prediction of COVID-19 in-hospital mortality in older patients using artificial intelligence: a multicenter study. The 3 I's of immunity and aging: immunosenescence, inflammaging, and immune resilience.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1