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动态原子力显微镜检测低密度脂蛋白在氧化诱导下大小、硬度和粘性的变化。

Dynamic AFM detection of the oxidation-induced changes in size, stiffness, and stickiness of low-density lipoprotein.

机构信息

Jiangxi Key Laboratory for Microscale interdisciplinary Study, Institute for Advanced Study, Nanchang University, Nanchang, 330031, Jiangxi, P. R. China.

School of Materials Science and Engineering, Nanchang University, 999 Xuefu Ave., Honggutan District, Nanchang, 330031, Jiangxi, P. R. China.

出版信息

J Nanobiotechnology. 2020 Nov 12;18(1):167. doi: 10.1186/s12951-020-00727-x.


DOI:10.1186/s12951-020-00727-x
PMID:33183326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7664080/
Abstract

BACKGROUND: Low-density lipoprotein (LDL) is an important plasma lipoprotein transporting lipids to peripheral tissues/cells. The oxidation of LDL plays critical roles in atherogenesis and its oxidized form (oxLDL) is an important risk factor of atherosclerosis. The biomechanical properties of LDL/oxLDL are closely correlated with the disease. To date, however, the oxidation-induced changes in size and biomechanical properties (stiffness and stickiness) of LDL particles are less investigated. METHODS: In this study, copper-induced LDL oxidation was confirmed by detecting electrophoretic mobility, malondialdehyde production, and conjugated diene formation. Then, the topographical and biomechanical mappings of LDL particles before/after and during oxidation were performed by using atomic force microscopy (AFM) and the size and biomechanical forces of particles were measured and quantitatively analyzed. RESULTS: Oxidation induced a significant decrease in size and stiffness (Young's modulus) but a significant increase in stickiness (adhesion force) of LDL particles. The smaller, softer, and stickier characteristics of oxidized LDL (oxLDL) partially explains its pro-atherosclerotic role. CONCLUSIONS: The data implies that LDL oxidation probably aggravates atherogenesis by changing the size and biomechanical properties of LDL particles. The data may provide important information for a better understanding of LDL/oxLDL and atherosclerosis.

摘要

背景:低密度脂蛋白(LDL)是一种重要的血浆脂蛋白,负责将脂质转运至外周组织/细胞。LDL 的氧化在动脉粥样硬化形成中起着关键作用,其氧化形式(oxLDL)是动脉粥样硬化的一个重要危险因素。LDL/oxLDL 的生物力学特性与该疾病密切相关。然而,迄今为止,LDL 颗粒的氧化诱导的大小和生物力学特性(刚性和粘性)变化研究较少。

方法:在这项研究中,通过检测电泳迁移率、丙二醛产生和共轭二烯形成来确认铜诱导的 LDL 氧化。然后,通过原子力显微镜(AFM)对 LDL 颗粒在氧化前后及氧化过程中的形貌和生物力学进行映射,并测量和定量分析颗粒的大小和生物力学力。

结果:氧化导致 LDL 颗粒的大小和刚性(杨氏模量)显著降低,但粘性(粘附力)显著增加。氧化 LDL(oxLDL)的更小、更软、更粘性的特征部分解释了其促动脉粥样硬化的作用。

结论:这些数据表明,LDL 氧化可能通过改变 LDL 颗粒的大小和生物力学特性来加重动脉粥样硬化形成。这些数据可能为更好地理解 LDL/oxLDL 和动脉粥样硬化提供重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/dab18bb7b6ec/12951_2020_727_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/a9ed5a933949/12951_2020_727_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/c67f1f46ef79/12951_2020_727_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/bc107c8832fa/12951_2020_727_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/dab18bb7b6ec/12951_2020_727_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/a9ed5a933949/12951_2020_727_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/c67f1f46ef79/12951_2020_727_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/bc107c8832fa/12951_2020_727_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4d/7664080/dab18bb7b6ec/12951_2020_727_Fig4_HTML.jpg

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本文引用的文献

[1]
Mapping the surface potential, charge density and adhesion of cellulose nanocrystals using advanced scanning probe microscopy.

Carbohydr Polym. 2020-10-15

[2]
Can atherosclerosis be cured?

Curr Opin Lipidol. 2019-12

[3]
Exogenous GM3 ganglioside inhibits atherosclerosis via multiple steps: A potential atheroprotective drug.

Pharmacol Res. 2019-9-14

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AFM assessing of nanomechanical fingerprints for cancer early diagnosis and classification: from single cell to tissue level.

Nanoscale. 2018-11-8

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Effects of enzymes on elastic modulus of low-density lipoproteins were investigated using atomic force microscopy.

Biochem Biophys Res Commun. 2018-6-27

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Comparative investigation on the sizes and scavenger receptor binding of human native and modified lipoprotein particles with atomic force microscopy.

J Nanobiotechnology. 2018-3-21

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Semin Cell Dev Biol. 2017-8-19

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In situ AFM imaging of apolipoprotein A-I directly derived from plasma HDL.

Atherosclerosis. 2017-4

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Effects of cyclodextrins on the structure of LDL and its susceptibility to copper-induced oxidation.

Eur J Pharm Sci. 2016-8-25

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