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胆固醇、脂蛋白与 COVID-19:基本概念与临床应用。

Cholesterol, lipoproteins, and COVID-19: Basic concepts and clinical applications.

机构信息

Centre for Functional Genomics and Bio-Chips, Institute of Biochemistry, Faculty of Medicine, University of Ljubljana, Zaloška 4, 1000 Ljubljana, Slovenia.

出版信息

Biochim Biophys Acta Mol Cell Biol Lipids. 2021 Feb;1866(2):158849. doi: 10.1016/j.bbalip.2020.158849. Epub 2020 Nov 4.


DOI:10.1016/j.bbalip.2020.158849
PMID:33157278
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7610134/
Abstract

Cholesterol is being recognized as a molecule involved in regulating the entry of the SARS-CoV-2 virus into the host cell. However, the data about the possible role of cholesterol carrying lipoproteins and their receptors in relation to infection are scarce and the connection of lipid-associated pathologies with COVID-19 disease is in its infancy. Herein we provide an overview of lipids and lipid metabolism in relation to COVID-19, with special attention on different forms of cholesterol. Cholesterol enriched lipid rafts represent a platform for viruses to enter the host cell by endocytosis. Generally, higher membrane cholesterol coincides with higher efficiency of COVID-19 entry. Inversely, patients with COVID-19 show lowered levels of blood cholesterol, high-density lipoproteins (HDL) and low-density lipoproteins. The modulated efficiency of viral entry can be explained by availability of SR-B1 receptor. HDL seems to have a variety of roles, from being itself a scavenger for viruses, an immune modulator and mediator of viral entry. Due to inverse roles of membrane cholesterol and lipoprotein cholesterol in COVID-19 infected patients, treatment of these patients with cholesterol lowering statins needs more attention. In conclusion, cholesterol and lipoproteins are potential markers for monitoring the viral infection status, while the lipid metabolic pathways and the composition of membranes could be targeted to selectively inhibit the life cycle of the virus as a basis for antiviral therapy.

摘要

胆固醇被认为是一种参与调节 SARS-CoV-2 病毒进入宿主细胞的分子。然而,关于胆固醇携带脂蛋白及其受体在感染中的可能作用的数据很少,脂质相关病理学与 COVID-19 疾病的联系还处于起步阶段。本文综述了与 COVID-19 相关的脂质和脂质代谢,特别关注不同形式的胆固醇。富含胆固醇的脂筏代表病毒通过内吞作用进入宿主细胞的平台。一般来说,较高的膜胆固醇与 COVID-19 进入的效率较高相一致。相反,COVID-19 患者的血液胆固醇、高密度脂蛋白 (HDL) 和低密度脂蛋白水平降低。病毒进入效率的调节可以用 SR-B1 受体的可用性来解释。HDL 似乎具有多种作用,它本身既是病毒的清除剂,又是免疫调节剂和病毒进入的介质。由于膜胆固醇和脂蛋白胆固醇在 COVID-19 感染患者中的作用相反,因此需要更多关注用降低胆固醇的他汀类药物治疗这些患者。总之,胆固醇和脂蛋白可能是监测病毒感染状态的潜在标志物,而脂质代谢途径和膜的组成可以作为抗病毒治疗的基础,针对病毒的生命周期进行选择性抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b06/7610134/9bd8240d42ee/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b06/7610134/9bd8240d42ee/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b06/7610134/9bd8240d42ee/gr1_lrg.jpg

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引用本文的文献

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Influence of Cholesterol on the Insertion and Interaction of SARS-CoV-2 Proteins with Lipid Membranes.

ACS Appl Bio Mater. 2025-6-16

[2]
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Surg Today. 2025-5

[3]
Proposed Mechanisms and Associations of COVID-19 with Cardiometabolic Risk Factors.

Am J Lifestyle Med. 2024-9-2

[4]
Phenotypic switch of vascular smooth muscle cells in COVID-19: Role of cholesterol, calcium, and phosphate.

J Cell Physiol. 2024-12

[5]
Lipoprotein particles exhibit distinct mechanical properties.

J Extracell Biol. 2022-12-18

[6]
Effect of IL-6R blockade on plasma lipids and clinical outcomes among hospitalized patients with COVID-19 infection.

J Lipid Res. 2024-6

[7]
Solid-liquid distribution of SARS-CoV-2 in primary effluent of a wastewater treatment plant.

MethodsX. 2024-3-11

[8]
Novel COVID-19 biomarkers identified through multi-omics data analysis: N-acetyl-4-O-acetylneuraminic acid, N-acetyl-L-alanine, N-acetyltriptophan, palmitoylcarnitine, and glycerol 1-myristate.

Intern Emerg Med. 2024-8

[9]
Associations of Temporal Cardiometabolic Patterns and Incident SARS-CoV-2 Infection Among U.S. Blood Donors With Serologic Evidence of Vaccination.

AJPM Focus. 2024-1-8

[10]
Research Advances on the Role of Lipids in the Life Cycle of Human Coronaviruses.

Microorganisms. 2023-12-28

本文引用的文献

[1]
COVID-19-activated SREBP2 disturbs cholesterol biosynthesis and leads to cytokine storm.

Signal Transduct Target Ther. 2020-9-3

[2]
Interaction Between Coronavirus S-Protein and Human ACE2: Hints for Exploring Efficient Therapeutic Targets to Treat COVID-19.

Angiology. 2021-2

[3]
The cholesterol metabolite 27-hydroxycholesterol inhibits SARS-CoV-2 and is markedly decreased in COVID-19 patients.

Redox Biol. 2020-8-10

[4]
Mevalonate pathway, selenoproteins, redox balance, immune system, Covid-19: Reasoning about connections.

Med Hypotheses. 2020-7-21

[5]
Cytokine Storm in COVID-19-Immunopathological Mechanisms, Clinical Considerations, and Therapeutic Approaches: The REPROGRAM Consortium Position Paper.

Front Immunol. 2020-7-10

[6]
Cholesterol in Relation to COVID-19: Should We Care about It?

J Clin Med. 2020-6-18

[7]
Potential COVID-19 therapeutics from a rare disease: weaponizing lipid dysregulation to combat viral infectivity.

J Lipid Res. 2020-5-26

[8]
Hypolipidemia is associated with the severity of COVID-19.

J Clin Lipidol. 2020-4-30

[9]
The Role of Lipid Metabolism in COVID-19 Virus Infection and as a Drug Target.

Int J Mol Sci. 2020-5-17

[10]
Statins and the COVID-19 main protease: evidence on direct interaction.

Arch Med Sci. 2020-4-25

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