• 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

长链非编码 RNA 将氧化型低密度脂蛋白与动脉粥样硬化中巨噬细胞的炎症反应联系起来。

Long Non-Coding RNAs Link Oxidized Low-Density Lipoprotein With the Inflammatory Response of Macrophages in Atherogenesis.

机构信息

Department of Cardiology, Second Hospital of Jilin University, Changchun, China.

Key Laboratory of Myocardial Ischemia, Ministry of Education, Harbin Medical University, Harbin, China.

出版信息

Front Immunol. 2020 Jan 30;11:24. doi: 10.3389/fimmu.2020.00024. eCollection 2020.

DOI:10.3389/fimmu.2020.00024
PMID:32082313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7003668/
Abstract

Atherosclerosis is characterized as a chronic inflammatory response to cholesterol deposition in arteries. Low-density lipoprotein (LDL), especially the oxidized form (ox-LDL), plays a crucial role in the occurrence and development of atherosclerosis by inducing endothelial cell (EC) dysfunction, attracting monocyte-derived macrophages, and promoting chronic inflammation. However, the mechanisms linking cholesterol accumulation with inflammation in macrophage foam cells are poorly understood. Long non-coding RNAs (lncRNAs) are a group of non-protein-coding RNAs longer than 200 nucleotides and are found to regulate the progress of atherosclerosis. Recently, many lncRNAs interfering with cholesterol deposition or inflammation were identified, which might help elucidate their underlying molecular mechanism or be used as novel therapeutic targets. In this review, we summarize and highlight the role of lncRNAs linking cholesterol (mainly ox-LDL) accumulation with inflammation in macrophages during the process of atherosclerosis.

摘要

动脉粥样硬化的特征是胆固醇在动脉中的沉积引发的慢性炎症反应。低密度脂蛋白(LDL),尤其是氧化形式(ox-LDL),通过诱导内皮细胞(EC)功能障碍、吸引单核细胞来源的巨噬细胞和促进慢性炎症,在动脉粥样硬化的发生和发展中起着关键作用。然而,胆固醇积累与巨噬细胞泡沫细胞中炎症之间的联系的机制尚不清楚。长链非编码 RNA(lncRNA)是一组长度超过 200 个核苷酸的非蛋白编码 RNA,被发现可以调节动脉粥样硬化的进展。最近,许多干扰胆固醇沉积或炎症的 lncRNA 被鉴定出来,这可能有助于阐明其潜在的分子机制,或可作为新的治疗靶点。在这篇综述中,我们总结并强调了 lncRNA 在动脉粥样硬化过程中连接胆固醇(主要是 ox-LDL)积累与巨噬细胞炎症的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e71b/7003668/23869f355859/fimmu-11-00024-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e71b/7003668/23869f355859/fimmu-11-00024-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e71b/7003668/23869f355859/fimmu-11-00024-g0001.jpg

相似文献

1
Long Non-Coding RNAs Link Oxidized Low-Density Lipoprotein With the Inflammatory Response of Macrophages in Atherogenesis.长链非编码 RNA 将氧化型低密度脂蛋白与动脉粥样硬化中巨噬细胞的炎症反应联系起来。
Front Immunol. 2020 Jan 30;11:24. doi: 10.3389/fimmu.2020.00024. eCollection 2020.
2
RP5-833A20.1/miR-382-5p/NFIA-dependent signal transduction pathway contributes to the regulation of cholesterol homeostasis and inflammatory reaction.RP5-833A20.1/miR-382-5p/核因子IA依赖的信号转导通路有助于胆固醇稳态和炎症反应的调节。
Arterioscler Thromb Vasc Biol. 2015 Jan;35(1):87-101. doi: 10.1161/ATVBAHA.114.304296. Epub 2014 Aug 14.
3
Inclisiran inhibits oxidized low-density lipoprotein-induced foam cell formation in Raw264.7 macrophages via activating the PPARγ pathway.依洛昔兰通过激活 PPARγ 通路抑制氧化型低密度脂蛋白诱导的 Raw264.7 巨噬细胞泡沫细胞形成。
Autoimmunity. 2022 Jun;55(4):223-232. doi: 10.1080/08916934.2022.2051142. Epub 2022 Mar 15.
4
Clematichinenoside AR Alleviates Foam Cell Formation and the Inflammatory Response in Ox-LDL-Induced RAW264.7 Cells by Activating Autophagy.滇藏木兰苷元 AR 通过激活自噬减轻氧化型低密度脂蛋白诱导的 RAW264.7 细胞泡沫细胞形成和炎症反应。
Inflammation. 2021 Apr;44(2):758-768. doi: 10.1007/s10753-020-01375-x. Epub 2020 Nov 5.
5
Long Noncoding RNA HOXC-AS1 Suppresses Ox-LDL-Induced Cholesterol Accumulation Through Promoting HOXC6 Expression in THP-1 Macrophages.长链非编码RNA HOXC-AS1通过促进THP-1巨噬细胞中HOXC6的表达来抑制氧化型低密度脂蛋白诱导的胆固醇积累。
DNA Cell Biol. 2016 Nov;35(11):722-729. doi: 10.1089/dna.2016.3422. Epub 2016 Aug 30.
6
Silence of long intergenic noncoding RNA HOTAIR ameliorates oxidative stress and inflammation response in ox-LDL-treated human macrophages by upregulating miR-330-5p.长链非编码 RNA HOTAIR 的沉默通过上调 miR-330-5p 减轻 ox-LDL 处理的人巨噬细胞中的氧化应激和炎症反应。
J Cell Physiol. 2019 Apr;234(4):5134-5142. doi: 10.1002/jcp.27317. Epub 2018 Sep 6.
7
Blockade of NEAT1 represses inflammation response and lipid uptake via modulating miR-342-3p in human macrophages THP-1 cells.NEAT1 阻断通过调节人巨噬细胞 THP-1 细胞中的 miR-342-3p 抑制炎症反应和脂质摄取。
J Cell Physiol. 2019 Apr;234(4):5319-5326. doi: 10.1002/jcp.27340. Epub 2018 Sep 27.
8
Long noncoding RNA THRIL promotes foam cell formation and inflammation in macrophages.长链非编码RNA THRIL促进巨噬细胞中泡沫细胞的形成和炎症反应。
Cell Biol Int. 2023 Jan;47(1):156-166. doi: 10.1002/cbin.11934. Epub 2022 Oct 13.
9
LncRBA GSA5, up-regulated by ox-LDL, aggravates inflammatory response and MMP expression in THP-1 macrophages by acting like a sponge for miR-221.LncRBA GSA5 在氧化低密度脂蛋白(ox-LDL)的作用下被上调,通过充当 miR-221 的海绵体,加剧了 THP-1 巨噬细胞的炎症反应和 MMP 表达。
Exp Cell Res. 2018 Aug 15;369(2):348-355. doi: 10.1016/j.yexcr.2018.05.039. Epub 2018 May 31.
10
Tribbles Homolog 3 Promotes Foam Cell Formation Associated with Decreased Proinflammatory Cytokine Production in Macrophages: Evidence for Reciprocal Regulation of Cholesterol Uptake and Inflammation.Tribbles同源物3促进巨噬细胞中与促炎细胞因子产生减少相关的泡沫细胞形成:胆固醇摄取与炎症相互调节的证据
Metab Syndr Relat Disord. 2016 Feb;14(1):7-15. doi: 10.1089/met.2015.0037. Epub 2015 Nov 19.

引用本文的文献

1
Long noncoding RNAs in familial hypercholesterolemia: biomarkers, therapeutics, and AI in precision medicine.家族性高胆固醇血症中的长链非编码RNA:精准医学中的生物标志物、治疗方法及人工智能
Lipids Health Dis. 2025 May 21;24(1):182. doi: 10.1186/s12944-025-02605-7.
2
Neutrophil Extracellular Traps in Atherosclerosis: Research Progress.动脉粥样硬化中的中性粒细胞胞外陷阱:研究进展
Int J Mol Sci. 2025 Mar 6;26(5):2336. doi: 10.3390/ijms26052336.
3
Antioxidant and Anti-Inflammatory Effects of Bioactive Compounds in Atherosclerosis.生物活性化合物在动脉粥样硬化中的抗氧化和抗炎作用

本文引用的文献

1
Long non-coding RNA CDKN2B-AS1 contributes to atherosclerotic plaque formation by forming RNA-DNA triplex in the CDKN2B promoter.长非编码 RNA CDKN2B-AS1 通过在 CDKN2B 启动子中形成 RNA-DNA 三链体促进动脉粥样硬化斑块形成。
EBioMedicine. 2020 May;55:102694. doi: 10.1016/j.ebiom.2020.102694. Epub 2020 Apr 24.
2
The long noncoding RNA CHROME regulates cholesterol homeostasis in primate.长链非编码 RNA CHROME 调节灵长类动物的胆固醇稳态。
Nat Metab. 2019 Jan;1(1):98-110. doi: 10.1038/s42255-018-0004-9. Epub 2018 Dec 3.
3
LncRNA MEG3-derived miR-361-5p regulate vascular smooth muscle cells proliferation and apoptosis by targeting ABCA1.
Int J Mol Sci. 2025 Feb 6;26(3):1379. doi: 10.3390/ijms26031379.
4
Effect of Extract on Foam Cell Formation in THP-1 Macrophages.提取物对THP-1巨噬细胞中泡沫细胞形成的影响。
Prev Nutr Food Sci. 2024 Sep 30;29(3):288-300. doi: 10.3746/pnf.2024.29.3.288.
5
The lncRNA GAS5 upregulates ANXA2 to mediate the macrophage inflammatory response during atherosclerosis development.长链非编码RNA GAS5上调膜联蛋白A2以介导动脉粥样硬化发展过程中的巨噬细胞炎症反应。
Heliyon. 2024 Jan 4;10(2):e24103. doi: 10.1016/j.heliyon.2024.e24103. eCollection 2024 Jan 30.
6
Non-Coding RNAs in Regulating Plaque Progression and Remodeling of Extracellular Matrix in Atherosclerosis.非编码 RNA 在调控动脉粥样硬化斑块进展和细胞外基质重塑中的作用。
Int J Mol Sci. 2022 Nov 8;23(22):13731. doi: 10.3390/ijms232213731.
7
A bibliometric analysis of autophagy in atherosclerosis from 2012 to 2021.2012年至2021年动脉粥样硬化中自噬的文献计量分析。
Front Pharmacol. 2022 Sep 15;13:977870. doi: 10.3389/fphar.2022.977870. eCollection 2022.
8
Exploring the Mangrove Fruit: From the Phytochemicals to Functional Food Development and the Current Progress in the Middle East.探索红树林果实:从植物化学物质到功能性食品开发以及在中东的最新进展。
Mar Drugs. 2022 Apr 28;20(5):303. doi: 10.3390/md20050303.
9
The role of long noncoding RNA Nron in atherosclerosis development and plaque stability.长链非编码RNA Nron在动脉粥样硬化发展和斑块稳定性中的作用。
iScience. 2022 Feb 24;25(3):103978. doi: 10.1016/j.isci.2022.103978. eCollection 2022 Mar 18.
10
Overexpression of miR-126 Protects Hypoxic-Reoxygenation-Exposed HUVEC Cellular Injury through Regulating LRP6 Expression.miR-126 的过表达通过调节 LRP6 表达来保护缺氧复氧暴露的 HUVEC 细胞损伤。
Oxid Med Cell Longev. 2022 Jan 17;2022:3647744. doi: 10.1155/2022/3647744. eCollection 2022.
长链非编码RNA MEG3衍生的miR-361-5p通过靶向ABCA1调控血管平滑肌细胞的增殖和凋亡。
Am J Transl Res. 2019 Jun 15;11(6):3600-3609. eCollection 2019.
4
The lncRNA DAPK-IT1 regulates cholesterol metabolism and inflammatory response in macrophages and promotes atherogenesis.长链非编码 RNA DAPK-IT1 调控巨噬细胞中的胆固醇代谢和炎症反应,并促进动脉粥样硬化形成。
Biochem Biophys Res Commun. 2019 Sep 3;516(4):1234-1241. doi: 10.1016/j.bbrc.2019.06.113. Epub 2019 Jul 9.
5
Up-regulation of MIAT aggravates the atherosclerotic damage in atherosclerosis mice through the activation of PI3K/Akt signaling pathway.上调 MIAT 通过激活 PI3K/Akt 信号通路加重动脉粥样硬化小鼠的动脉粥样硬化损伤。
Drug Deliv. 2019 Dec;26(1):641-649. doi: 10.1080/10717544.2019.1628116.
6
LncRNA-MIAT Increased in Patients with Coronary Atherosclerotic Heart Disease.长链非编码RNA-MIAT在冠状动脉粥样硬化性心脏病患者中表达升高。
Cardiol Res Pract. 2019 Apr 16;2019:6280194. doi: 10.1155/2019/6280194. eCollection 2019.
7
LncRNA H19/miR-let-7 axis participates in the regulation of ox-LDL-induced endothelial cell injury via targeting periostin.长链非编码 RNA H19/miR-let-7 轴通过靶向骨膜蛋白参与调控氧化型低密度脂蛋白诱导的内皮细胞损伤。
Int Immunopharmacol. 2019 Jul;72:496-503. doi: 10.1016/j.intimp.2019.04.042. Epub 2019 May 1.
8
Ox-LDL-induced lncRNA MALAT1 promotes autophagy in human umbilical vein endothelial cells by sponging miR-216a-5p and regulating Beclin-1 expression.Ox-LDL 诱导的长链非编码 RNA MALAT1 通过海绵吸附 miR-216a-5p 并调节 Beclin-1 表达促进人脐静脉内皮细胞自噬。
Eur J Pharmacol. 2019 Sep 5;858:172338. doi: 10.1016/j.ejphar.2019.04.019. Epub 2019 Apr 25.
9
LncRNA ENST00000602558.1 regulates ABCG1 expression and cholesterol efflux from vascular smooth muscle cells through a p65-dependent pathway.LncRNA ENST00000602558.1 通过依赖 p65 的途径调节 ABCG1 表达和血管平滑肌细胞中的胆固醇外排。
Atherosclerosis. 2019 Jun;285:31-39. doi: 10.1016/j.atherosclerosis.2019.04.204. Epub 2019 Apr 8.
10
LncRNA AC096664.3/PPAR-γ/ABCG1-dependent signal transduction pathway contributes to the regulation of cholesterol homeostasis.LncRNA AC096664.3/PPAR-γ/ABCG1 依赖性信号转导通路参与胆固醇稳态的调控。
J Cell Biochem. 2019 Aug;120(8):13775-13782. doi: 10.1002/jcb.28650. Epub 2019 Apr 2.