A morphometric study on human muscle mitochondria in aging.

Carlo Bertoni-Freddari, Patrizia Fattoretti, Ugo Caselli, Belinda Giorgetti, Stefano Albanelli, Francesco Torelli, Giorgio Felzani, Jacopo Vecchiet
{"title":"A morphometric study on human muscle mitochondria in aging.","authors":"Carlo Bertoni-Freddari,&nbsp;Patrizia Fattoretti,&nbsp;Ugo Caselli,&nbsp;Belinda Giorgetti,&nbsp;Stefano Albanelli,&nbsp;Francesco Torelli,&nbsp;Giorgio Felzani,&nbsp;Jacopo Vecchiet","doi":"10.1007/s11357-002-0008-x","DOIUrl":null,"url":null,"abstract":"<p><p>Mitochondria are dynamic organelles capable of significant changes of their ultrastructural features according to the tissue-specific energy demands. In human biopsies of vastus lateralis and anterior tibialis muscles from young (25.0 ± 4.4 years), middle-aged (50.4 ± 7.5 years) and old (75.5±3.9 years) healthy volunteers, we carried out a morphometric study on subsarcolemmal and intermyofibrillar mitochondria to assess whether age-related alterations of the morphology of these organelles contribute to the muscle performance decay in aging. By computer-assisted methods, we measured: the average area (MAA), the longer diameter (Dmax) and the ratio perimeter to area (pleomorphic index: Plei) of mitochondria. No significant age-related ultrastructural differences were found either in subsarcolemmal or intermyofibrillar organelles. However, in middle-aged as well as in the old group of patients vs. the young one, MAA and Dmax showed a clear trend to decrease, while Plei showed a marked, age-related tendency to increase. Higher percentages of less pleomorphic organelles were found in the youngest group of patients and this was particularly evident in the subsarcolemmal mitochondrial population. In addition to reporting on discrete aspects of mitochondrial ultrastructure, MAA, Dmax and Plei are closely related to each other and provide a reliable index of the muscle mitochondria adaptive response to age. Thus, we interpret our results as indicating a substantial preservation of muscle mitochondrial ultrastructure during aging.</p>","PeriodicalId":89818,"journal":{"name":"Journal of the American Aging Association","volume":"25 2","pages":"101-5"},"PeriodicalIF":0.0000,"publicationDate":"2002-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s11357-002-0008-x","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Aging Association","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s11357-002-0008-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7

Abstract

Mitochondria are dynamic organelles capable of significant changes of their ultrastructural features according to the tissue-specific energy demands. In human biopsies of vastus lateralis and anterior tibialis muscles from young (25.0 ± 4.4 years), middle-aged (50.4 ± 7.5 years) and old (75.5±3.9 years) healthy volunteers, we carried out a morphometric study on subsarcolemmal and intermyofibrillar mitochondria to assess whether age-related alterations of the morphology of these organelles contribute to the muscle performance decay in aging. By computer-assisted methods, we measured: the average area (MAA), the longer diameter (Dmax) and the ratio perimeter to area (pleomorphic index: Plei) of mitochondria. No significant age-related ultrastructural differences were found either in subsarcolemmal or intermyofibrillar organelles. However, in middle-aged as well as in the old group of patients vs. the young one, MAA and Dmax showed a clear trend to decrease, while Plei showed a marked, age-related tendency to increase. Higher percentages of less pleomorphic organelles were found in the youngest group of patients and this was particularly evident in the subsarcolemmal mitochondrial population. In addition to reporting on discrete aspects of mitochondrial ultrastructure, MAA, Dmax and Plei are closely related to each other and provide a reliable index of the muscle mitochondria adaptive response to age. Thus, we interpret our results as indicating a substantial preservation of muscle mitochondrial ultrastructure during aging.

衰老过程中人体肌肉线粒体形态计量学研究。
线粒体是一种动态细胞器,能够根据组织特异性能量需求显著改变其超微结构特征。在年轻(25.0±4.4岁)、中年(50.4±7.5岁)和老年(75.5±3.9岁)健康志愿者的股外侧肌和胫骨前肌活检中,我们对肌层下和肌纤维间线粒体进行了形态计量学研究,以评估这些细胞器的年龄相关形态学改变是否会导致肌肉性能衰退。通过计算机辅助方法,我们测量了线粒体的平均面积(MAA)、长径(Dmax)和周长比(Plei)。肌层下和肌纤维间细胞器的超微结构均未见明显的年龄相关差异。然而,与年轻组相比,中老年组MAA和Dmax有明显的下降趋势,而Plei有明显的随年龄增加的趋势。在最年轻的一组患者中发现了更高比例的多形性细胞器,这在肌层下线粒体群体中尤为明显。除了报道线粒体超微结构的离散方面外,MAA、Dmax和Plei彼此密切相关,并提供了肌肉线粒体对年龄适应性反应的可靠指标。因此,我们将我们的结果解释为表明在衰老过程中肌肉线粒体超微结构的大量保存。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书