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                  <mods:namePart>Vazquez, Jesus</mods:namePart>
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                  <mods:namePart>Martin-Ventura, Jose Luis</mods:namePart>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
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                  <mods:namePart>Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)</mods:namePart>
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                  <mods:namePart>Fundación La Caixa</mods:namePart>
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               <mods:identifier type="citation">EBioMedicine. 2019; 43:43-53</mods:identifier>
               <mods:identifier type="doi">10.1016/j.ebiom.2019.04.012</mods:identifier>
               <mods:identifier type="e-issn">2352-3964</mods:identifier>
               <mods:identifier type="issn">23523964</mods:identifier>
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               <mods:abstract>BACKGROUND: High-density lipoproteins (HDL) are a complex mixture of lipids and proteins with vasculoprotective properties. However, HDL components could suffer post-translational modifications (PTMs) under pathological conditions, leading to dysfunctional HDL. We studied whether HDL are modified in abdominal aortic aneurysm (AAA) and the effect on HDL functionality. METHODS: HDL were isolated by ultracentrifugation from AAA tissue (HDL-T) and from plasma of healthy volunteers and then incubated with AAA tissue-conditioned medium (HDL-AAA CM). PTMs from these particles were characterized using Comet-PTM. The ability of HDL-AAA CM for promoting cholesterol efflux was determined ex vivo and in vivo by using J774A.1 [3H]cholesterol-labeled mouse macrophages and after injecting [3H]cholesterol-labeled mouse macrophages and HDL into the peritoneal cavity of wild-type C57BL/6 mice, respectively. Trp50 and Trp108 oxidized forms of APOA1 in HDL incubated with conditioned-medium of activated neutrophils and in plasma of AAA patients and controls were measured by targeted parallel reaction monitoring. FINDINGS: Oxidation was the most prevalent PTM in apolipoproteins, particularly in APOA1. Trp50 and Trp108 in APOA1 were the residues most clearly affected by oxidation in HDL-T and in HDL-AAA CM, when compared to their controls. In addition, cholesterol efflux was decreased in macrophages incubated with HDL-AAA CM in vitro and a decreased macrophage-to-serum reverse cholesterol transport was also observed in mice injected with HDL-AAA CM. Finally, both oxidized Trp50 and Trp108 forms of APOA1 were increased in HDL incubated with conditioned-medium of activated neutrophils and in plasma of AAA patients in relation to controls. INTERPRETATION: Oxidative modifications of HDL present in AAA tissue and plasma were closely associated with the loss of vasculoprotective properties of HDL in AAA. FUND: MINECO, ISCiii-FEDER, CIBERDEM, CIBERCV and LA CAIXA.</mods:abstract>
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                  <mods:topic>Abdominal aortic aneurysm</mods:topic>
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               <mods:subject>
                  <mods:topic>Biomarkers</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Cholesterol efflux</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>HDL</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Oxidative stress</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Proteomics</mods:topic>
               </mods:subject>
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                  <mods:title>APOA1 oxidation is associated to dysfunctional high-density lipoproteins in human abdominal aortic aneurysm</mods:title>
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         <div TYPE="DSpace BITSTREAM">
            <fptr FILEID="BITSTREAM_ORIGINAL_20.500.12105_7851_1"/>
         </div>
         <div TYPE="DSpace BITSTREAM">
            <fptr FILEID="BITSTREAM_ORIGINAL_20.500.12105_7851_2"/>
         </div>
      </div>
   </structMap>
</mets></metadata></record></GetRecord></OAI-PMH>