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      Lipoproteins as targets and markers of lipoxidation

      review-article
      , *
      Redox Biology
      Elsevier
      AGEs, advanced glycation end products, ALEs, advanced lipoxidation end products, Apo, Apolipoprotein, COL, Nε-(8-carboxyoctanyl)-Lysine, DNPH, 2,4-dinitrophenylhydrazine, ELISA, enzyme-linked immunosorbent assay, GC-MS, gas chromatography mass spectrometry, HDDE, 4-hydroxy-2E,6Z-dodecadienal, HDL, high density lipoprotein, HHE, 4-hydroxy-trans-2-hexenal, HNE, 4-hydroxy-trans-2-nonenal, HOCl, hypochlorous acid, HPNE, 4-hydroperoxy-trans-2-nonenal, IDL, intermediate density lipoprotein, 3-HOSCA, 3β-hydroxy-5-oxo-5,6-secocholestan-6-al, KLH, keyhole limpet hemocyanin, HPLC-ESI-MSMS, (high pressure) liquid chromatography (electrospray) (tandem) mass spectrometry , LDL, low density lipoprotein, Lp(a), lipoprotein(a), MALDI-TOF, matrix-assisted laser desorption ionization time of flight, MDA, malondialdehyde, MS, mass spectrometry, OSE, oxidation-specific epitope, oxLDL/HDL, oxidized low/high density lipoprotein, (ox)PC, (oxidized) phosphatidylcholine, (ox)PL, (oxidized) phospholipid, PAH, polycyclic aromatic hydrocarbons, PL, phospholipid, PONPC, 1-palmitoyl-2-(9-oxo-nonanoyl)-sn-glycero-3-phosphocholine, POVPC, 1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphorylcholine, rLPPs, reactive lipid peroxidation products, TBArS, thiobarbituric acid reactive substances, TNBS, 2,4,6-trinitrobenzene sulfonic acid, VLDL, very low density lipoprotein, LDL, HDL, ApoB-100, Lipid peroxidation, Liquid chromatography mass spectrometry, Immunoassays, Atherosclerosis

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          Abstract

          Lipoproteins are essential systemic lipid transport particles, composed of apolipoproteins embedded in a phospholipid and cholesterol monolayer surrounding a cargo of diverse lipid species. Many of the lipids present are susceptible to oxidative damage by lipid peroxidation, giving rise to the formation of reactive lipid peroxidation products (rLPPs). In view of the close proximity of the protein and lipid moieties within lipoproteins, the probability of adduct formation between rLPPs and amino acid residues of the proteins, a process called lipoxidation, is high. There has been interest for many years in the biological effects of such modifications, but the field has been limited to some extent by the availability of methods to determine the sites and exact nature of such modification. More recently, the availability of a wide range of antibodies to lipoxidation products, as well as advances in analytical techniques such as liquid chromatography tandem mass spectrometry (LC-MSMS), have increased our knowledge substantially. While most work has focused on LDL, oxidation of which has long been associated with pro-inflammatory responses and atherosclerosis, some studies on HDL, VLDL and Lipoprotein(a) have also been reported. As the broader topic of LDL oxidation has been reviewed previously, this review focuses on lipoxidative modifications of lipoproteins, from the historical background through to recent advances in the field. We consider the main methods of analysis for detecting rLPP adducts on apolipoproteins, including their advantages and disadvantages, as well as the biological effects of lipoxidized lipoproteins and their potential roles in diseases.

          Graphical abstract

          Highlights

          • Lipoproteins can be modified by reactive Lipid Peroxidation Products (rLPPs).

          • Lipoprotein lipoxidation is known to occur in several inflammatory diseases.

          • Biochemical, immunochemical and mass spectrometry methods can detect rLPP adducts.

          • Due to higher information output, MS can facilitate localization of modifications.

          • Antibodies against some rLPPs have been used to identify lipoxidation in vivo.

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          Most cited references134

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          The distribution and chemical composition of ultracentrifugally separated lipoproteins in human serum.

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            • Article: not found

            Low density lipoprotein oxidation and its pathobiological significance.

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              • Article: not found

              Lipid peroxidation of membrane phospholipids generates hydroxy-alkenals and oxidized phospholipids active in physiological and/or pathological conditions.

              Polyunsaturated fatty acids (PUFAs) and their metabolites have a variety of physiological roles including: energy provision, membrane structure, cell signaling and regulation of gene expression. Lipids containing polyunsaturated fatty acids are susceptible to free radical-initiated oxidation and can participate in chain reactions that increase damage to biomolecules. Lipid peroxidation, which leads to lipid hydroperoxide formation often, occurs in response to oxidative stress. Hydroperoxides are usually reduced to their corresponding alcohols by glutathione peroxidases. However, these enzymes are decreased in certain diseases resulting in a temporary increase of lipid hydroperoxides that favors their degradation into several compounds, including hydroxy-alkenals. The best known of these are: 4-hydroxy-2-nonenal (4-HNE) and 4-hydroxy-2-hexenal (4-HHE), which derive from lipid peroxidation of n-6 and n-3 fatty acids, respectively. Compared to free radicals, these aldehydes are relatively stable and can diffuse within or even escape from the cell and attack targets far from the site of the original event. These aldehydes exhibit great reactivity with biomolecules, such as proteins, DNA, and phospholipids, generating a variety of intra and intermolecular covalent adducts. At the membrane level, proteins and amino lipids can be covalently modified by lipid peroxidation products (hydoxy-alkenals). These aldehydes can also act as bioactive molecules in physiological and/or pathological conditions. In addition this review is intended to provide an appropriate synopsis of identified effects of hydroxy-alkenals and oxidized phospholipids on cell signaling, from their intracellular production, to their action as intracellular messenger, up to their influence on transcription factors and gene expression.
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                Author and article information

                Contributors
                Journal
                Redox Biol
                Redox Biol
                Redox Biology
                Elsevier
                2213-2317
                06 December 2018
                May 2019
                06 December 2018
                : 23
                : 101066
                Affiliations
                [0005]School of Life and Health Sciences, Aston University, Aston Triangle, Aston University, Birmingham B4 7ET, UK
                Author notes
                [* ]Corresponding author. c.m.spickett@ 123456aston.ac.uk
                Article
                S2213-2317(18)31015-2 101066
                10.1016/j.redox.2018.101066
                6859580
                30579928
                f48a8b77-fb28-4d34-b0ca-8751262f8d2d
                © 2018 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 30 October 2018
                : 28 November 2018
                : 5 December 2018
                Categories
                Lipoxidation in pathophysiology and its assessment by high precision methodology

                ages, advanced glycation end products,ales, advanced lipoxidation end products,apo, apolipoprotein,col, nε-(8-carboxyoctanyl)-lysine,dnph, 2,4-dinitrophenylhydrazine,elisa, enzyme-linked immunosorbent assay,gc-ms, gas chromatography mass spectrometry,hdde, 4-hydroxy-2e,6z-dodecadienal,hdl, high density lipoprotein,hhe, 4-hydroxy-trans-2-hexenal,hne, 4-hydroxy-trans-2-nonenal,hocl, hypochlorous acid,hpne, 4-hydroperoxy-trans-2-nonenal,idl, intermediate density lipoprotein,3-hosca, 3β-hydroxy-5-oxo-5,6-secocholestan-6-al,klh, keyhole limpet hemocyanin,hplc-esi-msms, (high pressure) liquid chromatography (electrospray) (tandem) mass spectrometry,ldl, low density lipoprotein,lp(a), lipoprotein(a),maldi-tof, matrix-assisted laser desorption ionization time of flight,mda, malondialdehyde,ms, mass spectrometry,ose, oxidation-specific epitope,oxldl/hdl, oxidized low/high density lipoprotein,(ox)pc, (oxidized) phosphatidylcholine,(ox)pl, (oxidized) phospholipid,pah, polycyclic aromatic hydrocarbons,pl, phospholipid,ponpc, 1-palmitoyl-2-(9-oxo-nonanoyl)-sn-glycero-3-phosphocholine,povpc, 1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphorylcholine,rlpps, reactive lipid peroxidation products,tbars, thiobarbituric acid reactive substances,tnbs, 2,4,6-trinitrobenzene sulfonic acid,vldl, very low density lipoprotein,ldl,hdl,apob-100,lipid peroxidation,liquid chromatography mass spectrometry,immunoassays,atherosclerosis

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