Redox signalling: from nitric oxide to oxidized lipids.

Sruti Shiva, Doug Moellering, Anup Ramachandran, Anna-Liisa Levonen, Aimee Landar, Aparna Venkatraman, Erin Ceaser, Elena Ulasova, Jack H Crawford, Paul S Brookes, Rakesh P Patel, Victor M Darley-Usmar
{"title":"Redox signalling: from nitric oxide to oxidized lipids.","authors":"Sruti Shiva,&nbsp;Doug Moellering,&nbsp;Anup Ramachandran,&nbsp;Anna-Liisa Levonen,&nbsp;Aimee Landar,&nbsp;Aparna Venkatraman,&nbsp;Erin Ceaser,&nbsp;Elena Ulasova,&nbsp;Jack H Crawford,&nbsp;Paul S Brookes,&nbsp;Rakesh P Patel,&nbsp;Victor M Darley-Usmar","doi":"10.1042/bss0710107","DOIUrl":null,"url":null,"abstract":"<p><p>Cellular redox signalling is mediated by the post-translational modification of proteins in signal-transduction pathways by ROS/RNS (reactive oxygen species/reactive nitrogen species) or the products derived from their reactions. NO is perhaps the best understood in this regard with two important modifications of proteins known to induce conformational changes leading to modulation of function. The first is the addition of NO to haem groups as shown for soluble guanylate cyclase and the newly discovered NO/cytochrome c oxidase signalling pathway in mitochondria. The second mechanism is through the modification of thiols by NO to form an S-nitrosated species. Other ROS/RNS can also modify signalling proteins although the mechanisms are not as clearly defined. For example, electrophilic lipids, formed as the reaction products of oxidation reactions, orchestrate adaptive responses in the vasculature by reacting with nucleophilic cysteine residues. In modifying signalling proteins ROS/RNS appear to change the overall activity of signalling pathways in a process that we have termed 'redox tone'. In this review, we discuss these different mechanisms of redox cell signalling, and give specific examples of ROS/RNS participation in signal transduction.</p>","PeriodicalId":55383,"journal":{"name":"Biochemical Society Symposia","volume":" 71","pages":"107-20"},"PeriodicalIF":0.0000,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"39","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Society Symposia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1042/bss0710107","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 39

Abstract

Cellular redox signalling is mediated by the post-translational modification of proteins in signal-transduction pathways by ROS/RNS (reactive oxygen species/reactive nitrogen species) or the products derived from their reactions. NO is perhaps the best understood in this regard with two important modifications of proteins known to induce conformational changes leading to modulation of function. The first is the addition of NO to haem groups as shown for soluble guanylate cyclase and the newly discovered NO/cytochrome c oxidase signalling pathway in mitochondria. The second mechanism is through the modification of thiols by NO to form an S-nitrosated species. Other ROS/RNS can also modify signalling proteins although the mechanisms are not as clearly defined. For example, electrophilic lipids, formed as the reaction products of oxidation reactions, orchestrate adaptive responses in the vasculature by reacting with nucleophilic cysteine residues. In modifying signalling proteins ROS/RNS appear to change the overall activity of signalling pathways in a process that we have termed 'redox tone'. In this review, we discuss these different mechanisms of redox cell signalling, and give specific examples of ROS/RNS participation in signal transduction.

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
氧化还原信号:从一氧化氮到氧化脂质。
细胞氧化还原信号是通过ROS/RNS(活性氧/活性氮)或其反应产物对信号转导通路中蛋白质的翻译后修饰介导的。在这方面,NO可能是最好的理解,已知有两种重要的蛋白质修饰可以诱导构象变化导致功能调节。第一种是在血红素群中添加NO,如可溶性鸟苷酸环化酶和线粒体中新发现的NO/细胞色素c氧化酶信号通路。第二种机制是通过NO对硫醇的修饰形成s -亚硝化物质。其他ROS/RNS也可以修饰信号蛋白,但其机制尚不明确。例如,作为氧化反应产物形成的亲电性脂质,通过与亲核半胱氨酸残基反应,在脉管系统中协调适应性反应。在改变信号蛋白的过程中,ROS/RNS似乎改变了信号通路的整体活性,我们称之为“氧化还原张力”。在这篇综述中,我们讨论了这些氧化还原细胞信号传导的不同机制,并给出了ROS/RNS参与信号转导的具体例子。
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
自引率
0.00%
发文量
0
期刊最新文献
Pleckstrin homology (PH) domains and phosphoinositides. Evolutionarily conserved structural and functional roles of the FYVE domain. The role of the phosphoinositides at the Golgi complex. PtdIns5P: a little phosphoinositide with big functions? Our FABulous VACation: a decade of phosphatidylinositol 3,5-bisphosphate.
×
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