Cited by 176Cholesterol and Lipid MetabolismParaoxonase enzyme and polymorphismsLipoproteins and Cardiovascular Health

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Structural modifications of HDL and functional consequences

Ferretti, Gianna, Bacchetti, Tiziana, Nègre-Salvayre, Anne, Salvayre, Robert, Dousset, Nicole, Curatola, Giovanna·2006·Atherosclerosis

DOI 10.1016/j.atherosclerosis.2005.08.008

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Abstract

High density lipoproteins (HDL) are susceptible to structural modifications mediated by various mechanisms including oxidation, glycation, homocysteinylation or enzymatic degradation. Structural alterations of HDL may affect their functional and atheroprotective properties. Oxidants, such as hypochlorous acid, peroxyl radicals, metal ions, peroxynitrite, lipoxygenases and smoke extracts, can alter both surface and core components of HDL. The formation of lipid peroxidation derivatives, such as thiobarbituric acid reactive substances, conjugated dienes, lipid hydroperoxides and aldehydes, is associated with changes of physical properties (fluidity, molecular order) and of apoprotein conformation. Non-enzymatic glycation, generally associated with lipoxidation, leads to form irreversible complexes called advanced glycation end products. These HDL modifications are accompanied with altered biological activities of HDL and associated enzymes, including paraoxonase, CETP and LCAT. Homocysteine-induced modification of HDL is mediated by homocysteine-thiolactone, and can be prevented by a calcium-dependent thiolactonase/paraoxonase. Tyrosylation of HDL induces the formation of dimers and trimers of apo AI, and alters cholesterol efflux. Phospholipases and proteolytic enzymes can also modify HDL lipid and apoprotein structure. HDL modification induces generally the loss of their anti-inflammatory and cytoprotective properties. This could play a role in the pathogenesis of atherosclerosis and neurodegenerative diseases such as Alzheimer's disease.

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Authors: Ferretti, G., Bacchetti, T., Nègre-Salvayre, A., Salvayre, R., Dousset, N., & Curatola, G.
Affiliations: Inserm (FR)
Université Toulouse III - Paul Sabatier (FR)
Corresponding author: Ferretti, Gianna
ORCID: Ferretti, Gianna
Bacchetti, Tiziana
Curatola, Giovanna
Venue: Atherosclerosis
Publisher: Elsevier BV
Published: 2006-01
Volume: 184
Issue: 1
Pages: 1-7
ISSN: 0021-9150 (ISSN-L)
DOI: 10.1016/j.atherosclerosis.2005.08.008
OpenAlex: W2085222803
Cited by: 176
References: 70
Citations by year: 2026: 2 · 2025: 4 · 2024: 2 · 2023: 7 · 2022: 8 · 2021: 2 · 2020: 9 · 2019: 11 · 2018: 3 · 2017: 9 · 2016: 5 · 2015: 9 · 2014: 9 · 2013: 9 · 2012: 6
FWCI: 2.38
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Atherosclerosis (publishedVersion)
PubMed (publishedVersion)
Università Politecnica delle Marche (Università Politecnica delle Marche) (submittedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Paraoxonase enzyme and polymorphisms
Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
Keywords: high-density lipoprotein, HDL oxidation, lipid peroxidation, glycation, advanced glycation end products, homocysteine thiolactone, paraoxonase, cholesteryl ester transfer protein, lecithin:cholesterol acyltransferase, cholesterol efflux, anti-inflammatory activity, Alzheimer's disease, neurodegenerative diseases
MeSH terms: Antioxidants, Humans, Cholesterol, HDL, Lipid Peroxidation, Atherosclerosis

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Structural modifications of HDL and functional consequences

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