4.7 Article

Phospholipidome of endothelial cells shows a different adaptation response upon oxidative, glycative and lipoxidative stress

Journal

SCIENTIFIC REPORTS
Volume 8, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-018-30695-0

Keywords

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Funding

  1. European Commission [675132]
  2. CSIC
  3. University of Aveiro
  4. FCT/MEC
  5. European Union
  6. QREN
  7. COMPETE [FCT UID/QUI/00062/2013]
  8. FEDER [LISBOA-01-0145-FEDER-402-022125]
  9. Post-Doc grant [BPD/UI 51/5388/2017]
  10. Spanish MINECO/FEDER [SAF2015-68590-R]
  11. Instituto de Salud Carlos III/FEDER
  12. RETIC Aradyal [RD16/0006/0021]
  13. COST Action [CM1001]

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Endothelial dysfunction has been widely associated with oxidative stress, glucotoxicity and lipotoxicity and underlies the development of cardiovascular diseases (CVDs), atherosclerosis and diabetes. In such pathological conditions, lipids are emerging as mediators of signalling pathways evoking key cellular responses as expression of proinflammatory genes, proliferation and apoptosis. Hence, the assessment of lipid profiles in endothelial cells (EC) can provide valuable information on the molecular alterations underlying CVDs, atherosclerosis and diabetes. We performed a lipidomic approach based on hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) for the analysis of the phospholipidome of bovine aortic EC (BAEC) exposed to oxidative (H2O2), glycative (glucose), or lipoxidative (4-hydroxynonenal, HNE) stress. The phospholipid (PL) profile was evaluated for the classes PC, PE, PS, PG, PI, SM, LPC and CL. H2O2 induced a more acute adaptation of the PL profile than glucose or HNE. Unsaturated PL molecular species were up-regulated after 24 h incubation with H2O2, while an opposite trend was observed in glucose-and HNE-treated cells. This study compared, for the first time, the adaptation of the phospholipidome of BAEC upon different induced biochemical stresses. Although further biological studies will be necessary, our results unveil specific lipid signatures in response to characteristic types of stress.

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