EBioMedicine (May 2019)

APOA1 oxidation is associated to dysfunctional high-density lipoproteins in human abdominal aortic aneurysmResearch in context

  • Diego Martínez-López,
  • Emilio Camafeita,
  • Lídia Cedó,
  • Raquel Roldan-Montero,
  • Inmaculada Jorge,
  • Fernando García-Marqués,
  • María Gómez-Serrano,
  • Elena Bonzon-Kulichenko,
  • Francisco Blanco-Vaca,
  • Luis Miguel Blanco-Colio,
  • Jean-Baptiste Michel,
  • Joan Carles Escola-Gil,
  • Jesús Vázquez,
  • Jose Luis Martin-Ventura

Journal volume & issue
Vol. 43
pp. 43 – 53

Abstract

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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. Keywords: Abdominal aortic aneurysm, HDL, Oxidative stress, Proteomics, Cholesterol efflux, Biomarkers