人类衰老过程中骨骼肌mtDNA的定性和定量变化及线粒体编码基因的表达

Antoni Barrientos , Jordi Casademont , Francesc Cardellach , Esther Ardite , Xavier Estivill , Alvaro Urbano-Márquez , J.Carlos Fernández-Checa , Virginia Nunes
{"title":"人类衰老过程中骨骼肌mtDNA的定性和定量变化及线粒体编码基因的表达","authors":"Antoni Barrientos ,&nbsp;Jordi Casademont ,&nbsp;Francesc Cardellach ,&nbsp;Esther Ardite ,&nbsp;Xavier Estivill ,&nbsp;Alvaro Urbano-Márquez ,&nbsp;J.Carlos Fernández-Checa ,&nbsp;Virginia Nunes","doi":"10.1006/bmme.1997.2647","DOIUrl":null,"url":null,"abstract":"<div><p>It has been widely postulated that age-dependent changes in the mitochondrial genetic system may contribute to the human aging process. We recently reported unchanged specific activities of mitochondrial respiratory chain enzymes and a decrease in oxidation capacity of different substrates with aging, due, in part, to some confounding variables such as physical activity or tobacco consumption. The present study deals with age-related changes in muscle mtDNA structure and its biogenesis in humans. We found a low prevalence of mtDNA rearrangements with aging, only detected by PCR. The mtDNA content increased significantly with age (<em>b</em>= 0.0115,<em>P</em>&lt; 0.0001). Also, an unchanged steady-state level of mitochondrial transcripts, a reduced transcription rate (<em>P</em>&lt; 0.0001), and an increase in mitochondrial membrane lipid peroxidation (<em>P</em>&lt; 0.0001) were observed in aging. These data demonstrate that minor structural mtDNA changes appear during the human aging process. By contrast, alterations in mitochondrial homeostasis ultimately producing modifications in mitochondrial biogenesis rates could play a role in the process of human senescence.</p></div>","PeriodicalId":8837,"journal":{"name":"Biochemical and molecular medicine","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1997-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/bmme.1997.2647","citationCount":"89","resultStr":"{\"title\":\"Qualitative and Quantitative Changes in Skeletal Muscle mtDNA and Expression of Mitochondrial-Encoded Genes in the Human Aging Process\",\"authors\":\"Antoni Barrientos ,&nbsp;Jordi Casademont ,&nbsp;Francesc Cardellach ,&nbsp;Esther Ardite ,&nbsp;Xavier Estivill ,&nbsp;Alvaro Urbano-Márquez ,&nbsp;J.Carlos Fernández-Checa ,&nbsp;Virginia Nunes\",\"doi\":\"10.1006/bmme.1997.2647\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>It has been widely postulated that age-dependent changes in the mitochondrial genetic system may contribute to the human aging process. We recently reported unchanged specific activities of mitochondrial respiratory chain enzymes and a decrease in oxidation capacity of different substrates with aging, due, in part, to some confounding variables such as physical activity or tobacco consumption. The present study deals with age-related changes in muscle mtDNA structure and its biogenesis in humans. We found a low prevalence of mtDNA rearrangements with aging, only detected by PCR. The mtDNA content increased significantly with age (<em>b</em>= 0.0115,<em>P</em>&lt; 0.0001). Also, an unchanged steady-state level of mitochondrial transcripts, a reduced transcription rate (<em>P</em>&lt; 0.0001), and an increase in mitochondrial membrane lipid peroxidation (<em>P</em>&lt; 0.0001) were observed in aging. These data demonstrate that minor structural mtDNA changes appear during the human aging process. By contrast, alterations in mitochondrial homeostasis ultimately producing modifications in mitochondrial biogenesis rates could play a role in the process of human senescence.</p></div>\",\"PeriodicalId\":8837,\"journal\":{\"name\":\"Biochemical and molecular medicine\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1997-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1006/bmme.1997.2647\",\"citationCount\":\"89\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemical and molecular medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1077315097926478\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical and molecular medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1077315097926478","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 89

摘要

人们普遍认为,线粒体遗传系统的年龄依赖性变化可能有助于人类衰老过程。我们最近报道了线粒体呼吸链酶的特定活性不变,不同底物的氧化能力随着年龄的增长而下降,部分原因是一些混杂变量,如体育活动或烟草消费。目前的研究涉及与年龄相关的肌肉mtDNA结构的变化及其在人类的生物发生。我们发现mtDNA重排随年龄增长的发生率较低,仅通过PCR检测到。mtDNA含量随年龄的增长而显著增加(b= 0.0115,P<0.0001)。此外,线粒体转录物的稳态水平不变,转录率降低(P<0.0001),线粒体膜脂过氧化增加(P<0.0001)。这些数据表明,在人类衰老过程中出现了微小的mtDNA结构变化。相比之下,线粒体稳态的改变最终导致线粒体生物发生速率的改变,可能在人类衰老过程中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Qualitative and Quantitative Changes in Skeletal Muscle mtDNA and Expression of Mitochondrial-Encoded Genes in the Human Aging Process

It has been widely postulated that age-dependent changes in the mitochondrial genetic system may contribute to the human aging process. We recently reported unchanged specific activities of mitochondrial respiratory chain enzymes and a decrease in oxidation capacity of different substrates with aging, due, in part, to some confounding variables such as physical activity or tobacco consumption. The present study deals with age-related changes in muscle mtDNA structure and its biogenesis in humans. We found a low prevalence of mtDNA rearrangements with aging, only detected by PCR. The mtDNA content increased significantly with age (b= 0.0115,P< 0.0001). Also, an unchanged steady-state level of mitochondrial transcripts, a reduced transcription rate (P< 0.0001), and an increase in mitochondrial membrane lipid peroxidation (P< 0.0001) were observed in aging. These data demonstrate that minor structural mtDNA changes appear during the human aging process. By contrast, alterations in mitochondrial homeostasis ultimately producing modifications in mitochondrial biogenesis rates could play a role in the process of human senescence.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
EDITORIAL ANNOUNCEMENT Differential Effects of Wilms Tumor WT1 Splice Variants on the Insulin Receptor Promoter Hyperandrogenism and Manifesting Heterozygotes for 21-Hydroxylase Deficiency Analysis of the 5′ Flanking Region of the Human Galactocerebrosidase (GALC) Gene
×
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