心肌细胞特异性Piezo1缺乏通过保持线粒体稳态减轻缺血再灌注损伤。

IF 10.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Honglin Xu , Xin Chen , Shangfei Luo , Jintao Jiang , Xianmei Pan , Yu He , Bo Deng , Silin Liu , Rentao Wan , Liwen Lin , Qiaorui Tan , Xiaoting Chen , Youfen Yao , Bin He , Yajuan An , Jing Li
{"title":"心肌细胞特异性Piezo1缺乏通过保持线粒体稳态减轻缺血再灌注损伤。","authors":"Honglin Xu ,&nbsp;Xin Chen ,&nbsp;Shangfei Luo ,&nbsp;Jintao Jiang ,&nbsp;Xianmei Pan ,&nbsp;Yu He ,&nbsp;Bo Deng ,&nbsp;Silin Liu ,&nbsp;Rentao Wan ,&nbsp;Liwen Lin ,&nbsp;Qiaorui Tan ,&nbsp;Xiaoting Chen ,&nbsp;Youfen Yao ,&nbsp;Bin He ,&nbsp;Yajuan An ,&nbsp;Jing Li","doi":"10.1016/j.redox.2024.103471","DOIUrl":null,"url":null,"abstract":"<div><div>Ca<sup>2+</sup> overload and mitochondrial dysfunction play crucial roles in myocardial ischemia-reperfusion (I/R) injury. Piezo1, a mechanosensitive cation channel, is essential for intracellular Ca<sup>2+</sup> homeostasis. The objective of this research was to explore the effects of Piezo1 on mitochondrial function during myocardial I/R injury. We showed that the expression of myocardial Piezo1 was elevated in the infracted area of I/R and cardiomyocyte-specific <em>Piezo1</em> deficiency (<em>Piezo1</em><sup><em>△Myh6</em></sup>) mice attenuated I/R by decreasing infarct size and cardiac dysfunction. <em>Piezo1</em><sup><em>△Myh6</em></sup> regulated mitochondrial fusion and fission to improve mitochondrial function and decrease inflammation and oxidative stress <em>in vivo</em> and in vitro. Mechanistically, myocardial Piezo1 knockout alleviated intracellular calcium overload to normalize calpain-associated mitochondrial homeostasis. Our findings indicated that Piezo1 depletion in cardiomyocytes partially restored mitochondrial homeostasis during cardiac ischemia/reperfusion (I/R) injury. This study suggests an innovative therapeutic strategy to alleviate cardiac I/R injury.</div></div>","PeriodicalId":20998,"journal":{"name":"Redox Biology","volume":"79 ","pages":"Article 103471"},"PeriodicalIF":10.7000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11750285/pdf/","citationCount":"0","resultStr":"{\"title\":\"Cardiomyocyte-specific Piezo1 deficiency mitigates ischemia-reperfusion injury by preserving mitochondrial homeostasis\",\"authors\":\"Honglin Xu ,&nbsp;Xin Chen ,&nbsp;Shangfei Luo ,&nbsp;Jintao Jiang ,&nbsp;Xianmei Pan ,&nbsp;Yu He ,&nbsp;Bo Deng ,&nbsp;Silin Liu ,&nbsp;Rentao Wan ,&nbsp;Liwen Lin ,&nbsp;Qiaorui Tan ,&nbsp;Xiaoting Chen ,&nbsp;Youfen Yao ,&nbsp;Bin He ,&nbsp;Yajuan An ,&nbsp;Jing Li\",\"doi\":\"10.1016/j.redox.2024.103471\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Ca<sup>2+</sup> overload and mitochondrial dysfunction play crucial roles in myocardial ischemia-reperfusion (I/R) injury. Piezo1, a mechanosensitive cation channel, is essential for intracellular Ca<sup>2+</sup> homeostasis. The objective of this research was to explore the effects of Piezo1 on mitochondrial function during myocardial I/R injury. We showed that the expression of myocardial Piezo1 was elevated in the infracted area of I/R and cardiomyocyte-specific <em>Piezo1</em> deficiency (<em>Piezo1</em><sup><em>△Myh6</em></sup>) mice attenuated I/R by decreasing infarct size and cardiac dysfunction. <em>Piezo1</em><sup><em>△Myh6</em></sup> regulated mitochondrial fusion and fission to improve mitochondrial function and decrease inflammation and oxidative stress <em>in vivo</em> and in vitro. Mechanistically, myocardial Piezo1 knockout alleviated intracellular calcium overload to normalize calpain-associated mitochondrial homeostasis. Our findings indicated that Piezo1 depletion in cardiomyocytes partially restored mitochondrial homeostasis during cardiac ischemia/reperfusion (I/R) injury. This study suggests an innovative therapeutic strategy to alleviate cardiac I/R injury.</div></div>\",\"PeriodicalId\":20998,\"journal\":{\"name\":\"Redox Biology\",\"volume\":\"79 \",\"pages\":\"Article 103471\"},\"PeriodicalIF\":10.7000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11750285/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Redox Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S221323172400449X\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Redox Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S221323172400449X","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

Ca2+超载和线粒体功能障碍在心肌缺血再灌注(I/R)损伤中起重要作用。Piezo1是一种机械敏感的阳离子通道,对细胞内Ca2+稳态至关重要。本研究的目的是探讨Piezo1对心肌I/R损伤时线粒体功能的影响。我们发现心肌Piezo1在I/R梗死区表达升高,心肌细胞特异性Piezo1缺陷(Piezo1△Myh6)小鼠通过降低梗死面积和心功能障碍来减弱I/R。在体内和体外实验中,Piezo1△Myh6调节线粒体融合和裂变,改善线粒体功能,减少炎症和氧化应激。在机制上,心肌Piezo1基因敲除可减轻细胞内钙超载,使钙蛋白酶相关的线粒体稳态正常化。我们的研究结果表明,在心脏缺血/再灌注(I/R)损伤时,心肌细胞中Piezo1的缺失部分恢复了线粒体的稳态。本研究提出了一种减轻心脏I/R损伤的创新治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiomyocyte-specific Piezo1 deficiency mitigates ischemia-reperfusion injury by preserving mitochondrial homeostasis
Ca2+ overload and mitochondrial dysfunction play crucial roles in myocardial ischemia-reperfusion (I/R) injury. Piezo1, a mechanosensitive cation channel, is essential for intracellular Ca2+ homeostasis. The objective of this research was to explore the effects of Piezo1 on mitochondrial function during myocardial I/R injury. We showed that the expression of myocardial Piezo1 was elevated in the infracted area of I/R and cardiomyocyte-specific Piezo1 deficiency (Piezo1△Myh6) mice attenuated I/R by decreasing infarct size and cardiac dysfunction. Piezo1△Myh6 regulated mitochondrial fusion and fission to improve mitochondrial function and decrease inflammation and oxidative stress in vivo and in vitro. Mechanistically, myocardial Piezo1 knockout alleviated intracellular calcium overload to normalize calpain-associated mitochondrial homeostasis. Our findings indicated that Piezo1 depletion in cardiomyocytes partially restored mitochondrial homeostasis during cardiac ischemia/reperfusion (I/R) injury. This study suggests an innovative therapeutic strategy to alleviate cardiac I/R injury.
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
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
×
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