• 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

好胆固醇也能变坏事?HDL 与 COVID-19。

Good Cholesterol Gone Bad? HDL and COVID-19.

机构信息

Thrombosis and Atherosclerosis Research Institute and Department of Biochemistry and Biomedical Sciences, McMaster University and Hamilton Health Sciences, Hamilton, ON L8L 2X2, Canada.

出版信息

Int J Mol Sci. 2021 Sep 22;22(19):10182. doi: 10.3390/ijms221910182.

DOI:10.3390/ijms221910182
PMID:34638523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8507803/
Abstract

The transmissible respiratory disease COVID-19, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has affected millions of people worldwide since its first reported outbreak in December of 2019 in Wuhan, China. Since then, multiple studies have shown an inverse correlation between the levels of high-density lipoprotein (HDL) particles and the severity of COVID-19, with low HDL levels being associated with an increased risk of severe outcomes. Some studies revealed that HDL binds to SARS-CoV-2 particles via the virus's spike protein and, under certain conditions, such as low HDL particle concentrations, it facilitates SARS-CoV-2 binding to angiotensin-converting enzyme 2 (ACE2) and infection of host cells. Other studies, however, reported that HDL suppressed SARS-CoV-2 infection. In both cases, the ability of HDL to enhance or suppress virus infection appears to be dependent on the expression of the HDL receptor, namely, the Scavenger Receptor Class B type 1 (SR-B1), in the target cells. SR-B1 and HDL represent crucial mediators of cholesterol metabolism. Herein, we review the complex role of HDL and SR-B1 in SARS-CoV-2-induced disease. We also review recent advances in our understanding of HDL structure, properties, and function during SARS-CoV-2 infection and the resulting COVID-19 disease.

摘要

自 2019 年 12 月中国武汉首次报告爆发传染性呼吸道疾病 COVID-19 以来,由严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)引起的这种疾病已经影响了全球数百万人。此后,多项研究表明,高密度脂蛋白(HDL)颗粒水平与 COVID-19 的严重程度呈反比,HDL 水平低与严重后果的风险增加有关。一些研究表明,HDL 通过病毒的刺突蛋白与 SARS-CoV-2 颗粒结合,并且在某些条件下,例如 HDL 颗粒浓度低,它促进 SARS-CoV-2 与血管紧张素转换酶 2(ACE2)结合并感染宿主细胞。然而,其他研究报道 HDL 抑制了 SARS-CoV-2 感染。在这两种情况下,HDL 增强或抑制病毒感染的能力似乎取决于靶细胞中 HDL 受体(即 Scavenger Receptor Class B type 1,SR-B1)的表达。SR-B1 和 HDL 是胆固醇代谢的重要介质。在此,我们回顾了 HDL 和 SR-B1 在 SARS-CoV-2 诱导的疾病中的复杂作用。我们还回顾了最近在 SARS-CoV-2 感染期间对 HDL 结构、特性和功能的理解的最新进展,以及由此导致的 COVID-19 疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/3ed90b1f0c49/ijms-22-10182-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/3884c52ff20f/ijms-22-10182-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/9007da2edb0a/ijms-22-10182-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/a8063b95479a/ijms-22-10182-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/3ed90b1f0c49/ijms-22-10182-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/3884c52ff20f/ijms-22-10182-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/9007da2edb0a/ijms-22-10182-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/a8063b95479a/ijms-22-10182-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4162/8507803/3ed90b1f0c49/ijms-22-10182-g004.jpg

相似文献

1
Good Cholesterol Gone Bad? HDL and COVID-19.好胆固醇也能变坏事?HDL 与 COVID-19。
Int J Mol Sci. 2021 Sep 22;22(19):10182. doi: 10.3390/ijms221910182.
2
HDL-scavenger receptor B type 1 facilitates SARS-CoV-2 entry.HDL scavenger receptor B type 1 促进了 SARS-CoV-2 的进入。
Nat Metab. 2020 Dec;2(12):1391-1400. doi: 10.1038/s42255-020-00324-0. Epub 2020 Nov 26.
3
Cholesterol-Rich Lipid Rafts as Platforms for SARS-CoV-2 Entry.富含胆固醇的脂筏作为 SARS-CoV-2 进入的平台。
Front Immunol. 2021 Dec 16;12:796855. doi: 10.3389/fimmu.2021.796855. eCollection 2021.
4
The potential role of scavenger receptor B type I (SR-BI) in SARS-CoV-2 infection.清道夫受体 B 型 I(SR-BI)在 SARS-CoV-2 感染中的潜在作用。
Immun Inflamm Dis. 2023 Apr;11(4):e786. doi: 10.1002/iid3.786.
5
The expression of hACE2 receptor protein and its involvement in SARS-CoV-2 entry, pathogenesis, and its application as potential therapeutic target.hACE2 受体蛋白的表达及其在 SARS-CoV-2 进入、发病机制中的作用及其作为潜在治疗靶点的应用。
Tumour Biol. 2021;43(1):177-196. doi: 10.3233/TUB-200084.
6
SARS-CoV-2, ACE2 expression, and systemic organ invasion.严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)、血管紧张素转换酶 2(ACE2)表达与全身器官侵袭。
Physiol Genomics. 2021 Feb 1;53(2):51-60. doi: 10.1152/physiolgenomics.00087.2020. Epub 2020 Dec 4.
7
Contributions of human ACE2 and TMPRSS2 in determining host-pathogen interaction of COVID-19.人类血管紧张素转换酶2(ACE2)和跨膜丝氨酸蛋白酶2(TMPRSS2)在决定新型冠状病毒肺炎(COVID-19)宿主-病原体相互作用中的作用。
J Genet. 2021;100(1). doi: 10.1007/s12041-021-01262-w.
8
High-Density Lipoprotein function is modulated by the SARS-CoV-2 spike protein in a lipid-type dependent manner.高密度脂蛋白功能受 SARS-CoV-2 刺突蛋白调控,这种调控方式依赖于脂质类型。
J Colloid Interface Sci. 2023 Sep;645:627-638. doi: 10.1016/j.jcis.2023.04.137. Epub 2023 Apr 29.
9
Cross-Linking Mass Spectrometry Uncovers Interactions Between High-Density Lipoproteins and the SARS-CoV-2 Spike Glycoprotein.交联质谱法揭示了高密度脂蛋白与 SARS-CoV-2 刺突糖蛋白之间的相互作用。
Mol Cell Proteomics. 2023 Aug;22(8):100600. doi: 10.1016/j.mcpro.2023.100600. Epub 2023 Jun 19.
10
Hypochlorite-modified high density lipoprotein, a high affinity ligand to scavenger receptor class B, type I, impairs high density lipoprotein-dependent selective lipid uptake and reverse cholesterol transport.次氯酸盐修饰的高密度脂蛋白是I型清道夫受体B类的高亲和力配体,它会损害高密度脂蛋白依赖性的选择性脂质摄取和逆向胆固醇转运。
J Biol Chem. 2002 Aug 30;277(35):32172-9. doi: 10.1074/jbc.M200503200. Epub 2002 Jun 17.

引用本文的文献

1
COVID-19 and dysregulated cholesterol levels in Type I and Type II diabetes: focus on the difference.2型糖尿病和1型糖尿病中COVID-19与胆固醇水平失调:关注差异
Biol Futur. 2025 Aug 11. doi: 10.1007/s42977-025-00285-z.
2
The importance of paying attention to the role of lipid-lowering drugs in controlling dengue virus infection.重视降脂药物在控制登革病毒感染中作用的重要性。
Virol J. 2024 Dec 19;21(1):324. doi: 10.1186/s12985-024-02608-3.
3
The BNT162b2 mRNA vaccine demonstrates reduced age-associated T1 support and .BNT162b2信使核糖核酸疫苗显示出与年龄相关的T1支持减少,以及……(原文此处不完整)

本文引用的文献

1
Importance of Apolipoprotein A-I and A-II Composition in HDL and Its Potential for Studying COVID-19 and SARS-CoV-2.载脂蛋白A-I和A-II在高密度脂蛋白中的组成重要性及其在研究新型冠状病毒肺炎和严重急性呼吸综合征冠状病毒2方面的潜力
Medicines (Basel). 2021 Jul 16;8(7):38. doi: 10.3390/medicines8070038.
2
Highly accurate protein structure prediction with AlphaFold.利用 AlphaFold 进行高精度蛋白质结构预测。
Nature. 2021 Aug;596(7873):583-589. doi: 10.1038/s41586-021-03819-2. Epub 2021 Jul 15.
3
Association of pre-pandemic high-density lipoprotein cholesterol with risk of COVID-19 hospitalisation and death: The UK Biobank cohort study.
iScience. 2024 Sep 26;27(11):111055. doi: 10.1016/j.isci.2024.111055. eCollection 2024 Nov 15.
4
Neurological complications caused by SARS-CoV-2.新型冠状病毒(SARS-CoV-2)引起的神经并发症。
Clin Microbiol Rev. 2024 Dec 10;37(4):e0013124. doi: 10.1128/cmr.00131-24. Epub 2024 Sep 18.
5
Gene Cluster at 11q23.3 and Lipid Metabolism Disorders: From Epigenetic Mechanisms to Clinical Practices.11q23.3基因簇与脂质代谢紊乱:从表观遗传机制到临床实践
Biomedicines. 2024 May 31;12(6):1224. doi: 10.3390/biomedicines12061224.
6
Targeting the High-Density Lipoprotein Proteome for the Treatment of Post-Acute Sequelae of SARS-CoV-2.以高密度脂蛋白蛋白质组为靶点治疗新冠病毒急性后遗症
Int J Mol Sci. 2024 Apr 20;25(8):4522. doi: 10.3390/ijms25084522.
7
Longitudinal NMR-Based Metabolomics Study Reveals How Hospitalized COVID-19 Patients Recover: Evidence of Dyslipidemia and Energy Metabolism Dysregulation.基于纵向 NMR 的代谢组学研究揭示了住院 COVID-19 患者的康复情况:血脂异常和能量代谢失调的证据。
Int J Mol Sci. 2024 Jan 26;25(3):1523. doi: 10.3390/ijms25031523.
8
The dengue virus NS1 protein; new roles in pathogenesis due to similarities with and affinity for the high-density lipoprotein (HDL)?登革病毒NS1蛋白:因其与高密度脂蛋白(HDL)的相似性和亲和力而在发病机制中的新作用?
PLoS Pathog. 2023 Aug 24;19(8):e1011587. doi: 10.1371/journal.ppat.1011587. eCollection 2023 Aug.
9
Integrative Plasma Metabolic and Lipidomic Modelling of SARS-CoV-2 Infection in Relation to Clinical Severity and Early Mortality Prediction.整合 SARS-CoV-2 感染的血浆代谢组学和脂质组学模型与临床严重程度及早期死亡率预测的关系。
Int J Mol Sci. 2023 Jul 18;24(14):11614. doi: 10.3390/ijms241411614.
10
SARS-CoV-2 induced HDL dysfunction may affect the host's response to and recovery from COVID-19.SARS-CoV-2 诱导的高密度脂蛋白功能障碍可能影响宿主对 COVID-19 的反应和康复。
Immun Inflamm Dis. 2023 May;11(5):e861. doi: 10.1002/iid3.861.
疫情前高密度脂蛋白胆固醇与新冠病毒疾病住院及死亡风险的关联:英国生物银行队列研究
Prev Med Rep. 2021 Sep;23:101461. doi: 10.1016/j.pmedr.2021.101461. Epub 2021 Jun 23.
4
SARS-CoV-2 spike protein removes lipids from model membranes and interferes with the capacity of high density lipoprotein to exchange lipids.SARS-CoV-2 刺突蛋白从模型膜中去除脂质,并干扰高密度脂蛋白交换脂质的能力。
J Colloid Interface Sci. 2021 Nov 15;602:732-739. doi: 10.1016/j.jcis.2021.06.056. Epub 2021 Jun 12.
5
The role of abnormalities of lipoproteins and HDL functionality in small fibre dysfunction in people with severe obesity.脂蛋白异常和高密度脂蛋白功能障碍在严重肥胖人群小纤维功能障碍中的作用。
Sci Rep. 2021 Jun 15;11(1):12573. doi: 10.1038/s41598-021-90346-9.
6
Inherited Variants in Cause Severe Early-Onset Coronary Artery Disease.致病变异体导致严重早发性冠状动脉疾病。
Circ Res. 2021 Jul 9;129(2):296-307. doi: 10.1161/CIRCRESAHA.120.318793. Epub 2021 May 12.
7
The Endothelium Is Both a Target and a Barrier of HDL's Protective Functions.内皮既是 HDL 保护功能的靶点,也是其保护功能的屏障。
Cells. 2021 Apr 28;10(5):1041. doi: 10.3390/cells10051041.
8
Dependence of SARS-CoV-2 infection on cholesterol-rich lipid raft and endosomal acidification.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染对富含胆固醇的脂筏和内体酸化的依赖性。
Comput Struct Biotechnol J. 2021;19:1933-1943. doi: 10.1016/j.csbj.2021.04.001. Epub 2021 Apr 8.
9
Baseline cardiometabolic profiles and SARS-CoV-2 infection in the UK Biobank.英国生物银行的基线心血管代谢特征和 SARS-CoV-2 感染。
PLoS One. 2021 Apr 1;16(4):e0248602. doi: 10.1371/journal.pone.0248602. eCollection 2021.
10
SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE 2.严重急性呼吸综合征冠状病毒2刺突蛋白通过下调血管紧张素转换酶2损害内皮功能。
Circ Res. 2021 Apr 30;128(9):1323-1326. doi: 10.1161/CIRCRESAHA.121.318902. Epub 2021 Mar 31.