• 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

细胞焦亡在动脉粥样硬化中的作用及其治疗意义。

Role of pyroptosis in atherosclerosis and its therapeutic implications.

机构信息

Department of Cardiovascular Surgery, Peking University China-Japan Friendship School of Clinical Medicine, Beijing, China.

Department of Cardiovascular Surgery, China-Japan Friendship Hospital, Beijing, China.

出版信息

J Cell Physiol. 2021 Oct;236(10):7159-7175. doi: 10.1002/jcp.30366. Epub 2021 Mar 23.

DOI:10.1002/jcp.30366
PMID:33755211
Abstract

Atherosclerosis is a significant cardiovascular burden and a leading cause of death worldwide, recognized as a chronic sterile inflammatory disease. Pyroptosis is a novel proinflammatory regulated cell death, characterized by cell swelling, plasma membrane bubbling, and robust release of proinflammatory cytokines (such as interleukin IL-1β and IL-18). Mounting studies have addressed the crucial contribution of pyroptosis to atherosclerosis and clarified the candidate therapeutic agents targeting pyroptosis for atherosclerosis. Herein, we review the initial characterization of pyroptosis, the detailed mechanisms of pyroptosis, current evidence about pyroptosis and atherosclerosis, and potential therapeutic strategies that target pyroptosis in the development of atherosclerosis.

摘要

动脉粥样硬化是一种严重的心血管疾病负担,也是全球范围内的主要死亡原因,被认为是一种慢性非感染性炎症性疾病。细胞焦亡是一种新型的促炎调控性细胞死亡,其特征为细胞肿胀、细胞膜起泡和促炎细胞因子(如白细胞介素-1β和白细胞介素-18)的强烈释放。越来越多的研究表明细胞焦亡对动脉粥样硬化有重要贡献,并阐明了针对动脉粥样硬化的细胞焦亡治疗靶点候选药物。本文综述了细胞焦亡的初步特征、细胞焦亡的详细机制、细胞焦亡与动脉粥样硬化的现有证据,以及针对动脉粥样硬化发生过程中细胞焦亡的潜在治疗策略。

相似文献

1
Role of pyroptosis in atherosclerosis and its therapeutic implications.细胞焦亡在动脉粥样硬化中的作用及其治疗意义。
J Cell Physiol. 2021 Oct;236(10):7159-7175. doi: 10.1002/jcp.30366. Epub 2021 Mar 23.
2
The NLRP3 inflammasome and the emerging role of colchicine to inhibit atherosclerosis-associated inflammation.NLRP3 炎性小体与秋水仙碱抑制动脉粥样硬化相关炎症的新作用。
Atherosclerosis. 2018 Feb;269:262-271. doi: 10.1016/j.atherosclerosis.2017.12.027. Epub 2017 Dec 25.
3
Nicotine promotes atherosclerosis via ROS-NLRP3-mediated endothelial cell pyroptosis.尼古丁通过 ROS-NLRP3 介导的内皮细胞焦亡促进动脉粥样硬化。
Cell Death Dis. 2018 Feb 7;9(2):171. doi: 10.1038/s41419-017-0257-3.
4
The emerging role of pyroptosis-related inflammasome pathway in atherosclerosis.焦亡相关炎性小体通路在动脉粥样硬化中的新兴作用。
Mol Med. 2022 Dec 21;28(1):160. doi: 10.1186/s10020-022-00594-2.
5
Cell-Specific Roles of NLRP3 Inflammasome in Myocardial Infarction.NLRP3 炎性小体在心肌梗死中的细胞特异性作用。
J Cardiovasc Pharmacol. 2019 Sep;74(3):188-193. doi: 10.1097/FJC.0000000000000709.
6
Adiponectin alleviates NLRP3-inflammasome-mediated pyroptosis of aortic endothelial cells by inhibiting FoxO4 in arteriosclerosis.脂联素通过抑制动脉粥样硬化中的 FoxO4 减轻 NLRP3 炎性小体介导的主动脉内皮细胞焦亡。
Biochem Biophys Res Commun. 2019 Jun 18;514(1):266-272. doi: 10.1016/j.bbrc.2019.04.143. Epub 2019 Apr 25.
7
Atorvastatin inhibits pyroptosis through the lncRNA NEXN-AS1/NEXN pathway in human vascular endothelial cells.阿托伐他汀通过长链非编码 RNA NEXN-AS1/NEXN 通路抑制人血管内皮细胞焦亡。
Atherosclerosis. 2020 Jan;293:26-34. doi: 10.1016/j.atherosclerosis.2019.11.033. Epub 2019 Dec 3.
8
Low-dose Sinapic Acid Abates the Pyroptosis of Macrophages by Downregulation of lncRNA-MALAT1 in Rats With Diabetic Atherosclerosis.低剂量芥子酸通过下调糖尿病动脉粥样硬化大鼠lncRNA-MALAT1减轻巨噬细胞焦亡
J Cardiovasc Pharmacol. 2018 Feb;71(2):104-112. doi: 10.1097/FJC.0000000000000550.
9
Electrical stimulation inhibits Val-boroPro-induced pyroptosis in THP-1 macrophages via sirtuin3 activation to promote autophagy and inhibit ROS generation.电刺激通过激活 Sirtuin3 抑制 Val-boroPro 诱导的 THP-1 巨噬细胞焦亡,从而促进自噬并抑制 ROS 的产生。
Aging (Albany NY). 2020 Apr 14;12(7):6415-6435. doi: 10.18632/aging.103038.
10
MicroRNA-30c-5p inhibits NLRP3 inflammasome-mediated endothelial cell pyroptosis through FOXO3 down-regulation in atherosclerosis.miRNA-30c-5p 通过下调 FOXO3 抑制动脉粥样硬化中 NLRP3 炎性小体介导的内皮细胞焦亡
Biochem Biophys Res Commun. 2018 Sep 18;503(4):2833-2840. doi: 10.1016/j.bbrc.2018.08.049. Epub 2018 Aug 6.

引用本文的文献

1
Identification of pyroptosis related genes and subtypes in atherosclerosis using multiomic and single cell analysis.利用多组学和单细胞分析鉴定动脉粥样硬化中焦亡相关基因和亚型
Sci Rep. 2025 Jul 1;15(1):22360. doi: 10.1038/s41598-025-04398-2.
2
Anti-atherosclerotic effects and molecular targets of salvianolic acids from Bunge.来自 Bunge 的丹酚酸的抗动脉粥样硬化作用及分子靶点。
Front Pharmacol. 2025 May 21;16:1574086. doi: 10.3389/fphar.2025.1574086. eCollection 2025.
3
Targeting cholesterol-driven pyroptosis: a promising strategy for the prevention and treatment of atherosclerosis.
靶向胆固醇驱动的细胞焦亡:一种防治动脉粥样硬化的有前景策略。
Mol Biol Rep. 2025 May 15;52(1):459. doi: 10.1007/s11033-025-10554-8.
4
Isoorientin Ameliorates Macrophage Pyroptosis and Atherogenesis by Reducing KDM4A Levels and Promoting SKP1-Cullin1-F-box E3 Ligase-mediated NLRP3 Ubiquitination.异荭草素通过降低KDM4A水平并促进SKP1-Cullin1-F-box E3连接酶介导的NLRP3泛素化来改善巨噬细胞焦亡和动脉粥样硬化。
Inflammation. 2025 Mar 25. doi: 10.1007/s10753-025-02289-2.
5
Exosomes derived from baicalin‑pretreated mesenchymal stem cells mitigate atherosclerosis by regulating the SIRT1/NF‑κB signaling pathway.黄芩苷预处理间充质干细胞来源的外泌体通过调节SIRT1/NF-κB信号通路减轻动脉粥样硬化。
Mol Med Rep. 2025 May;31(5). doi: 10.3892/mmr.2025.13491. Epub 2025 Mar 14.
6
Pyroptosis-Mediator GSDMD in Plasma: A Promising Biomarker for Early Diagnosis of Type 2 Diabetes.血浆中焦亡介质GSDMD:一种用于2型糖尿病早期诊断的有前景的生物标志物。
Diabetes Metab Syndr Obes. 2025 Feb 14;18:453-464. doi: 10.2147/DMSO.S502336. eCollection 2025.
7
Pyroptosis in Endothelial Cells and Extracellular Vesicle Release in Atherosclerosis via NF-κB-Caspase-4/5-GSDM-D Pathway.通过NF-κB-半胱天冬酶-4/5-GSDM-D途径,内皮细胞中的焦亡与动脉粥样硬化中的细胞外囊泡释放
Pharmaceuticals (Basel). 2024 Nov 22;17(12):1568. doi: 10.3390/ph17121568.
8
FSCN1 is a Potential Therapeutic Target for Atherosclerosis Revealed by Single-Cell and Bulk RNA Sequencing.FSCN1是通过单细胞和批量RNA测序揭示的动脉粥样硬化的潜在治疗靶点。
J Inflamm Res. 2024 Nov 25;17:9683-9696. doi: 10.2147/JIR.S480528. eCollection 2024.
9
High-intensity interval training and moderate-intensity continuous training alleviate vascular dysfunction in spontaneously hypertensive rats through the inhibition of pyroptosis.高强度间歇训练和中等强度持续训练通过抑制细胞焦亡减轻自发性高血压大鼠的血管功能障碍。
Heliyon. 2024 Oct 19;10(21):e39505. doi: 10.1016/j.heliyon.2024.e39505. eCollection 2024 Nov 15.
10
Antiatherosclerotic Effect and Molecular Mechanism of Salidroside.红景天苷的抗动脉粥样硬化作用及分子机制
Rev Cardiovasc Med. 2023 Mar 23;24(4):97. doi: 10.31083/j.rcm2404097. eCollection 2023 Apr.