The innate immune response to products of phospholipid peroxidation☆
Autor: | Weismann, David, Binder, Christoph J. |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2012 |
Předmět: |
MFG-E8
Milk fat globule epidermal growth factor 8 (lactadherin) CEP carboxyethylpyrrole OxCL oxidized cardiolipin OxLDL oxidized LDL C# complement component # Damage-associated molecular pattern Apoptosis Review CHD coronary heart disease Biochemistry PAMP(s) pathogen-associated molecular pattern(s) Epitopes LDL low-density lipoprotein AMD age-related macular degeneration DAMP(s) damage-associated molecular pattern(s) POVPC 1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphcholine Phospholipids ApoE apolipoprotein E CFHR complement factor H related protein CPS capsular polysaccharide CuOx-LDL copper-oxidized LDL Receptors Pattern Recognition CRP C-reactive protein MAA malonacetaldehyde NAb(s) Natural antibodies FAAB 2-formyl-3-(alkylamino)butanal Oxidation-Reduction OxPS oxidized phosphatidylserine Oxidized LDL PUFA(s) polyunsaturated fatty acid(s) CL cardiolipin Lipid peroxidation Biophysics Pattern recognition receptor IL-# interleukin-# CFH complement factor H PE phosphatidylethanolamine HBGM1 high-mobility group box 1 4-HNE 4-hydroxynonenal Animals Humans PRR(s) pattern recognition receptor(s) TLR# toll-like receptor MDA malondialdehyde Cell Biology HSP(s) heat shock protein(s) AGE(s) advanced glycation end product(s) Immunity Innate RAG recombinase activating gene OSE(s) oxidation-specific epitope(s) BSA bovine serum albumin Oxidation-specific epitope MDHDC 4-methyl-1 4-dihydropyridine-3 5-dicarbaldehyde PC phosphocholine |
Zdroj: | Biochimica et Biophysica Acta |
ISSN: | 0006-3002 |
Popis: | Lipid peroxidation occurs in the context of many physiological processes but is greatly increased in various pathological situations. A consequence of phospholipid peroxidation is the generation of oxidation-specific epitopes, such as phosphocholine of oxidized phospholipids and malondialdehyde, which form neo-self determinants on dying cells and oxidized low-density lipoproteins. In this review we discuss evidence demonstrating that pattern recognition receptors of the innate immune system recognize oxidation-specific epitopes as endogenous damage-associated molecular patterns, allowing the host to identify dangerous biological waste. Oxidation-specific epitopes are important targets of both cellular and soluble pattern recognition receptors, including toll-like and scavenger receptors, C-reactive protein, complement factor H, and innate natural IgM antibodies. This recognition allows the innate immune system to mediate important physiological house keeping functions, for example by promoting the removal of dying cells and oxidized molecules. Once this system is malfunctional or overwhelmed the development of diseases, such as atherosclerosis and age-related macular degeneration is favored. Understanding the molecular components and mechanisms involved in this process, will help the identification of individuals with increased risk of developing chronic inflammation, and indicate novel points for therapeutic intervention. This article is part of a Special Issue entitled: Oxidized phospholipids—their properties and interactions with proteins. Highlights ► Phospholipid peroxidation results in the formation of oxidation-specific epitopes. ► Oxidation-specific epitopes are recognized by soluble and cellular pattern recognition receptors. ► Recognition by these receptors promotes the clearance of biological waste. ► This innate defense is challenged by increased oxidative stress, such as in chronic inflammation. |
Databáze: | OpenAIRE |
Externí odkaz: |