• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

线粒体代谢与动脉粥样硬化关系的新见解。

New insights into the relationship of mitochondrial metabolism and atherosclerosis.

作者信息

Wang Zexun, Sun Wangqing, Zhang Kai, Ke Xianjin, Wang Zhongqun

机构信息

Department of Cardiology, Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China; Institue of Cardiovascular Diseases, Jiangsu University, Zhenjiang 212001, China.

Department of Radiology, Yixing Tumor Hospital, Yixing 214200, China.

出版信息

Cell Signal. 2025 Mar;127:111580. doi: 10.1016/j.cellsig.2024.111580. Epub 2024 Dec 26.

DOI:10.1016/j.cellsig.2024.111580
PMID:39732307
Abstract

Atherosclerotic cardiovascular and cerebrovascular diseases are the number one killer of human health. In view of the important role of mitochondria in the formation and evolution of atherosclerosis, our manuscript aims to comprehensively elaborate the relationship between mitochondria and the formation and evolution of atherosclerosis from the aspects of mitochondrial dynamics, mitochondria-organelle interaction (communication), mitochondria and cell death, mitochondria and vascular smooth muscle cell phenotypic switch, etc., which is combined with genome, transcriptome and proteome, in order to provide new ideas for the pathogenesis of atherosclerosis and the diagnosis and treatment of related diseases.

摘要

动脉粥样硬化性心脑血管疾病是人类健康的头号杀手。鉴于线粒体在动脉粥样硬化形成和演变中的重要作用,我们的稿件旨在从线粒体动力学、线粒体-细胞器相互作用(通讯)、线粒体与细胞死亡、线粒体与血管平滑肌细胞表型转换等方面,结合基因组、转录组和蛋白质组,全面阐述线粒体与动脉粥样硬化形成和演变之间的关系,为动脉粥样硬化的发病机制及相关疾病的诊断和治疗提供新思路。

相似文献

1
New insights into the relationship of mitochondrial metabolism and atherosclerosis.线粒体代谢与动脉粥样硬化关系的新见解。
Cell Signal. 2025 Mar;127:111580. doi: 10.1016/j.cellsig.2024.111580. Epub 2024 Dec 26.
2
Mitochondrial Dysfunction in Atherosclerosis.线粒体功能障碍与动脉粥样硬化
DNA Cell Biol. 2019 Jul;38(7):597-606. doi: 10.1089/dna.2018.4552. Epub 2019 May 16.
3
Role of mitochondrial dynamics and mitophagy of vascular smooth muscle cell proliferation and migration in progression of atherosclerosis.线粒体动力学和血管平滑肌细胞自噬在动脉粥样硬化进展中的作用。
Arch Pharm Res. 2021 Dec;44(12):1051-1061. doi: 10.1007/s12272-021-01360-4. Epub 2021 Nov 7.
4
Mitochondria-targeted hydrogen sulfide donor reduces atherogenesis by changing macrophage phenotypes and increasing UCP1 expression in vascular smooth muscle cells.线粒体靶向硫化氢供体通过改变巨噬细胞表型和增加血管平滑肌细胞中 UCP1 的表达来减少动脉粥样硬化形成。
Biomed Pharmacother. 2024 Nov;180:117527. doi: 10.1016/j.biopha.2024.117527. Epub 2024 Oct 13.
5
Mitochondrion as a Selective Target for the Treatment of Atherosclerosis: Role of Mitochondrial DNA Mutations and Defective Mitophagy in the Pathogenesis of Atherosclerosis and Chronic Inflammation.线粒体作为动脉粥样硬化治疗的选择性靶标:线粒体 DNA 突变和有缺陷的线粒体自噬在动脉粥样硬化和慢性炎症发病机制中的作用。
Curr Neuropharmacol. 2020;18(11):1064-1075. doi: 10.2174/1570159X17666191118125018.
6
Mitochondrial Respiration Is Reduced in Atherosclerosis, Promoting Necrotic Core Formation and Reducing Relative Fibrous Cap Thickness.动脉粥样硬化中,线粒体呼吸作用减弱,促进坏死核心形成并减小相对纤维帽厚度。
Arterioscler Thromb Vasc Biol. 2017 Dec;37(12):2322-2332. doi: 10.1161/ATVBAHA.117.310042. Epub 2017 Sep 28.
7
Mitochondrial DAMPs and altered mitochondrial dynamics in OxLDL burden in atherosclerosis.线粒体 DAMPs 和氧化型低密度脂蛋白负担引起的动脉粥样硬化中线粒体动力学改变。
Mol Cell Biochem. 2021 Apr;476(4):1915-1928. doi: 10.1007/s11010-021-04061-0. Epub 2021 Jan 25.
8
Mitochondria spatially and temporally modulate VSMC phenotypes via interacting with cytoskeleton in cardiovascular diseases.线粒体通过与细胞骨架相互作用在心血管疾病中时空调节 VSMC 表型。
Redox Biol. 2023 Aug;64:102778. doi: 10.1016/j.redox.2023.102778. Epub 2023 Jun 7.
9
Inhibition of mitochondrial activity ameliorates atherosclerosis in ApoE mice via suppressing vascular smooth cell activation and macrophage foam cell formation.抑制线粒体活性通过抑制血管平滑肌细胞激活和巨噬细胞泡沫细胞形成来改善 ApoE 小鼠的动脉粥样硬化。
J Cell Biochem. 2019 Oct;120(10):17767-17778. doi: 10.1002/jcb.29042. Epub 2019 May 26.
10
Influence of glucose metabolism on vascular smooth muscle cell proliferation.葡萄糖代谢对血管平滑肌细胞增殖的影响。
Vasa. 2013 Jan;42(1):8-16. doi: 10.1024/0301-1526/a000243.

引用本文的文献

1
Genetic silencing of K3.1 inhibits atherosclerosis in ApoE null mice.K3.1的基因沉默可抑制载脂蛋白E基因敲除小鼠的动脉粥样硬化。
Channels (Austin). 2025 Dec;19(1):2538864. doi: 10.1080/19336950.2025.2538864. Epub 2025 Aug 3.
2
Endoplasmic reticulum-mitochondria crosstalk: new mechanisms in the development of atherosclerosis.内质网-线粒体相互作用:动脉粥样硬化发展的新机制
Front Endocrinol (Lausanne). 2025 Jun 5;16:1573499. doi: 10.3389/fendo.2025.1573499. eCollection 2025.
3
Apolipoprotein M delays the development of atherosclerosis by regulating autophagy and mitochondrial function.
载脂蛋白M通过调节自噬和线粒体功能延缓动脉粥样硬化的发展。
Cardiovasc Diagn Ther. 2025 Apr 30;15(2):423-440. doi: 10.21037/cdt-2024-614. Epub 2025 Apr 22.
4
Mitochondrial Dysfunction: A New Hallmark in Hereditable Thoracic Aortic Aneurysm Development.线粒体功能障碍:遗传性胸主动脉瘤发展中的一个新特征。
Cells. 2025 Apr 21;14(8):618. doi: 10.3390/cells14080618.
5
Current research on mitochondria‑associated membranes in cardiovascular diseases (Review).心血管疾病中线粒体相关膜的当前研究(综述)
Mol Med Rep. 2025 Jun;31(6). doi: 10.3892/mmr.2025.13506. Epub 2025 Apr 4.
6
Targeting Atherosclerosis via NEDD4L Signaling-A Review of the Current Literature.通过NEDD4L信号通路靶向动脉粥样硬化——当前文献综述
Biology (Basel). 2025 Feb 20;14(3):220. doi: 10.3390/biology14030220.