心脏肾上腺素能受体和 GRKs:心脏线粒体调节

IF 2.5 Q2 PHYSIOLOGY
Gizem Kayki-Mutlu, Ebru Arioglu-Inan
{"title":"心脏肾上腺素能受体和 GRKs:心脏线粒体调节","authors":"Gizem Kayki-Mutlu,&nbsp;Ebru Arioglu-Inan","doi":"10.1016/j.cophys.2023.100733","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>The cellular ‘powerhouse’, mitochondria play vital roles in cardiac cells, including the modulation of contractility. Among the various mechanisms, the modulation of cardiac mitochondria by adrenergic signaling stands out as a crucial component in orchestrating cardiac function. Adrenergic system serving as the primary regulator of </span>cardiac contractility, exerts its effects through α- and ß-adrenoceptors, which are regulated by G-protein-coupled receptor kinase 2 (GRK2) and ß-arrestin. In recent years, it has been revealed that these components of adrenergic signaling interact with mitochondria in diverse ways. α- and ß-adrenoceptors are reported to contribute to </span>mitochondrial biogenesis<span>, dynamics, and function. Besides, GRK2 is known to be localized to mitochondria, following oxidative stress or ischemic injury, and exerts negative metabolic effects. In this review, we outlined the contributions of these pivotal elements of adrenergic signaling to mitochondrial function. The better understanding of this delicate relationship holds crucial implications for novel therapeutic options to treat cardiovascular pathologies.</span></p></div>","PeriodicalId":52156,"journal":{"name":"Current Opinion in Physiology","volume":"37 ","pages":"Article 100733"},"PeriodicalIF":2.5000,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cardiac adrenergic receptors and GRKs: mitochondrial modulation in the heart\",\"authors\":\"Gizem Kayki-Mutlu,&nbsp;Ebru Arioglu-Inan\",\"doi\":\"10.1016/j.cophys.2023.100733\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>The cellular ‘powerhouse’, mitochondria play vital roles in cardiac cells, including the modulation of contractility. Among the various mechanisms, the modulation of cardiac mitochondria by adrenergic signaling stands out as a crucial component in orchestrating cardiac function. Adrenergic system serving as the primary regulator of </span>cardiac contractility, exerts its effects through α- and ß-adrenoceptors, which are regulated by G-protein-coupled receptor kinase 2 (GRK2) and ß-arrestin. In recent years, it has been revealed that these components of adrenergic signaling interact with mitochondria in diverse ways. α- and ß-adrenoceptors are reported to contribute to </span>mitochondrial biogenesis<span>, dynamics, and function. Besides, GRK2 is known to be localized to mitochondria, following oxidative stress or ischemic injury, and exerts negative metabolic effects. In this review, we outlined the contributions of these pivotal elements of adrenergic signaling to mitochondrial function. The better understanding of this delicate relationship holds crucial implications for novel therapeutic options to treat cardiovascular pathologies.</span></p></div>\",\"PeriodicalId\":52156,\"journal\":{\"name\":\"Current Opinion in Physiology\",\"volume\":\"37 \",\"pages\":\"Article 100733\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2023-12-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Opinion in Physiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468867323001049\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHYSIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Opinion in Physiology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468867323001049","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

线粒体是细胞的 "动力室",在心脏细胞中发挥着至关重要的作用,包括调节收缩力。在各种机制中,肾上腺素能信号对心脏线粒体的调节是协调心脏功能的重要组成部分。肾上腺素能系统是心脏收缩力的主要调节器,通过α-和ß-肾上腺素受体发挥作用,而α-和ß-肾上腺素受体又受 G 蛋白偶联受体激酶 2(GRK2)和ß-arrestin 的调节。据报道,α和ß肾上腺素受体有助于线粒体的生物生成、动力学和功能。此外,已知 GRK2 在氧化应激或缺血损伤后会定位到线粒体,并对新陈代谢产生负面影响。在这篇综述中,我们概述了肾上腺素能信号传导的这些关键因素对线粒体功能的贡献。更好地理解这种微妙的关系对治疗心血管疾病的新疗法具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiac adrenergic receptors and GRKs: mitochondrial modulation in the heart

The cellular ‘powerhouse’, mitochondria play vital roles in cardiac cells, including the modulation of contractility. Among the various mechanisms, the modulation of cardiac mitochondria by adrenergic signaling stands out as a crucial component in orchestrating cardiac function. Adrenergic system serving as the primary regulator of cardiac contractility, exerts its effects through α- and ß-adrenoceptors, which are regulated by G-protein-coupled receptor kinase 2 (GRK2) and ß-arrestin. In recent years, it has been revealed that these components of adrenergic signaling interact with mitochondria in diverse ways. α- and ß-adrenoceptors are reported to contribute to mitochondrial biogenesis, dynamics, and function. Besides, GRK2 is known to be localized to mitochondria, following oxidative stress or ischemic injury, and exerts negative metabolic effects. In this review, we outlined the contributions of these pivotal elements of adrenergic signaling to mitochondrial function. The better understanding of this delicate relationship holds crucial implications for novel therapeutic options to treat cardiovascular pathologies.

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
Current Opinion in Physiology
Current Opinion in Physiology Medicine-Physiology (medical)
CiteScore
5.80
自引率
0.00%
发文量
52
×
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:481959085
Book学术官方微信