4.7 Article

Low Concentrations of Oxidized Phospholipids Increase Stress Tolerance of Endothelial Cells

Journal

ANTIOXIDANTS
Volume 11, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/antiox11091741

Keywords

oxidized phospholipids; endothelial cell stress; cell survival

Funding

  1. Austrian Science Fund (FWF) [P27682, P35129]
  2. National Institute of Health [HL076259, HL146829, HL152761]
  3. Austrian Science Fund (FWF) [P35129, P27682] Funding Source: Austrian Science Fund (FWF)

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Oxidized phospholipids (OxPLs) can protect endothelial cells from stress-induced damage by extracting membrane cholesterol and inducing the expression of heat shock proteins and pro-survival factors.
Oxidized phospholipids (OxPLs) are generated by enzymatic or autooxidation of esterified polyunsaturated fatty acids (PUFAs) residues. OxPLs are present in circulation and atherosclerotic plaques where they are thought to induce predominantly proinflammatory and toxic changes in endothelial (ECs) and other cell types. Unexpectedly, we found that low concentrations of OxPLs were not toxic but protected ECs from stress induced by serum deprivation or cytostatic drugs. The protective effect was observed in ECs obtained from different vessels and was monitored using a variety of readouts based on different biological and chemical principles. Analysis of the structure-activity relationship identified oxidized or missing fatty acid residue (OxPLs or Lyso-PLs, respectively) as a prerequisite for the protective action of a PL. Protective OxPLs or Lyso-PLs acquired detergent-like properties and formed in solution aggregates <10 nm in diameter (likely micelles), which were in striking contrast with large aggregates (>1000 nm, likely multilayer liposomes) produced by nonoxidized precursor PLs. Because surfactants, OxPLs, and Lyso-PLs are known to extract membrane cholesterol, we tested if this effect might trigger the protection of endothelial cells. The protective action of OxPLs and Lyso-PLs was inhibited by cotreatment with cholesterol and mimicked by cholesterol-binding beta-cyclodextrin but not inactive alpha-cyclodextrin. Wide-scale mRNA expression analysis in four types of ECs showed the induction of genes encoding for heat shock proteins (HSPs) and secreted prosurvival peptides and proteins. Inducers of HSPs, chemical chaperones, and pure prosurvival factors mimicked the protective action of OxPLs/Lyso-PLs. We hypothesize that oxidation changes the physicochemical properties of PLs, thus promoting membrane cholesterol redistribution or extraction leading to the expression of intra- and extracellular prosurvival factors.

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