Nitro-oleic acid downregulates lipoprotein-associated phospholipase A2 expression via the p42/p44 MAPK and NFκB pathways

  • Gangqi Wang
  • , Yuan Ji
  • , Zhuang Li
  • , Xiaolei Han
  • , Nannan Guo
  • , Qi Song
  • , Longquan Quan
  • , Tiedong Wang
  • , Wenyu Han
  • , Daxin Pang
  • , Hongsheng Ouyang
  • , Xiaochun Tang

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Nitro-oleic acid (OA-NO2), acting as anti-inflammatory signaling mediators, are involved in multiple signaling pathways. Lipoprotein-associated phospholipase A2 (Lp-PLA2) is well known as a cardiovascular risk biomarker. Our results showed that OA-NO2 downregulated the expression of Lp-PLA2 in a time- and dose-dependent manner, whereas native OA had no such effect. Furthermore, OA-NO2 could repress Lp-PLA2 expression in the peripheral blood mononuclear cells of apo CIII-transgenic (apo CIII TG) pigs, which exhibited higher Lp-PLA2 expression and activity than did wild-type (WT) pigs. OA-NO2 inhibited Lp-PLA2 expression in macrophages, independent of nitric oxide formation and PPARγ-activation. However, OA-NO2 downregulates Lp-PLA2 by inhibiting the p42/p44 mitogen-activated protein kinase (MAPK) and the nuclear factor κB (NFκB) pathways. When used to mediate anti-inflammatory signaling, the regulation of inflammatory cytokines and SOD by OA-NO2 might be associated with the reduction of Lp-PLA2. These results suggested that OA-NO2 might exert a vascular-protective effect partially via Lp-PLA2 inhibition.

Original languageEnglish
Pages (from-to)4905
JournalScientific Reports
Volume4
DOIs
Publication statusPublished - 2014

Keywords

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • Animals
  • Cytokines
  • Down-Regulation
  • Gene Expression Regulation
  • Humans
  • Inflammation Mediators
  • Mitogen-Activated Protein Kinase 3
  • NF-kappa B
  • Nitric Oxide
  • Oleic Acid
  • PPAR gamma
  • Signal Transduction
  • Superoxide Dismutase
  • Swine

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