Eicosapentaenoic Acid (EPA) Induced Macrophages Activation through GPR120-Mediated Raf-ERK1/2-IKKβ-NF-κB p65 Signaling Pathways

Nutrients. 2017 Aug 25;9(9):937. doi: 10.3390/nu9090937.

Abstract

Objectives: To investigate the immunomodulatory effect and molecular mechanisms of Eicosapentaenoic acid (EPA, a typical kind of n-3PUFAs) on RAW264.7 cells. Methods: A variety of research methods, including the RAW264.7 cells culture, cell proliferation assays, morphologic observations, measurements of NO production, cytokine assays, nuclear protein extractions, western blot analyses and NF-κB p65 immunofluorescence assays were used in this study. Results: The results showed that EPA could increase the proliferation index and enhance the release of nitric oxide (NO) and cytokines in RAW264.7 cells. Western blotting results revealed that the protein level of GPR120 increased significantly in RAW264.7 cells after EPA treatment. Meanwhile, EPA elevated the phosphorylation status of Raf, which may act as an upstream regulator of EPA-induced phosphorylated ERK1/2. In addition, the phosphorylated ERK1/2 may then promote IKKβ in endochylema and translocate the NF-κB p65 subunit into the nucleus, thus regulating the production of inducible nitric oxide synthase (iNOS) and cytokines. Conclusions: EPA (0.6-3.0 μmol) activates RAW264.7 cells through GPR120-mediated Raf-ERK1/2-IKKβ-NF-κB p65 signaling pathways.

Keywords: Eicosapentaenoic acid; NF-κB; RAW264.7 cells; Raf; immunomodulatory.

MeSH terms

  • Active Transport, Cell Nucleus / drug effects
  • Animals
  • Cell Proliferation / drug effects
  • Cytokines / metabolism
  • Eicosapentaenoic Acid / metabolism*
  • I-kappa B Kinase / metabolism
  • Immunomodulation* / drug effects
  • MAP Kinase Signaling System* / drug effects
  • Macrophage Activation* / drug effects
  • Macrophages / cytology
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Mice
  • Models, Immunological*
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Phosphorylation / drug effects
  • Protein Kinase Inhibitors / pharmacology
  • Protein Processing, Post-Translational / drug effects
  • RAW 264.7 Cells
  • Receptors, G-Protein-Coupled / agonists*
  • Receptors, G-Protein-Coupled / metabolism
  • Transcription Factor RelA / antagonists & inhibitors
  • Transcription Factor RelA / metabolism

Substances

  • Cytokines
  • FFAR4 protein, mouse
  • Protein Kinase Inhibitors
  • Receptors, G-Protein-Coupled
  • Rela protein, mouse
  • Transcription Factor RelA
  • Nitric Oxide
  • Eicosapentaenoic Acid
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • I-kappa B Kinase
  • Ikbkb protein, mouse