Immunomodulation of ADPs-1a and ADPs-3a on RAW264.7 cells through NF-κB/MAPK signaling pathway

Int J Biol Macromol. 2019 Jul 1:132:1024-1030. doi: 10.1016/j.ijbiomac.2019.04.031. Epub 2019 Apr 5.

Abstract

ADPs-1a and ADPs-3a were two kinds of pure polysaccharide in Angelica dahurica. The immunomodulatory effects of ADPs-1a and ADPs-3a were assayed on phagocytosis, nitric oxide (NO) and cytokines of RAW264.7 cells, and the mechanism was investigated through NF-κB and MAPKs signaling pathway. RAW264.7 cells were stimulated by different concentrations of ADPs-1a and ADPs-3a with LPS (1 μg/mL) as positive control. The results showed that ADPs-1a and ADPs-3a could significantly enhance the phagocytic activity of RAW264.7 cells, and enhance the ability of RAW264.7 cells to release NO, TNF-α and IL-6 in a concentration-dependent manner. At the same time, ADPs-1a and ADPs-3a could significantly up-regulate the mRNA expression of iNOS, TNF-α, IL-6 and the phosphorylation level of p65, p38, ERK, JNK proteins. The immunomodulatory mechanism of ADPs-1a and ADPs-3a on macrophages was related to the up-regulation of phosphorylation of MAPKs and NF-kB.

Keywords: Angelica dahurica polysaccharide; Immunomodulation; MAPKs; NF-kB.

MeSH terms

  • Angelica / chemistry*
  • Animals
  • Cell Survival / drug effects
  • Gene Expression Regulation, Enzymologic / drug effects
  • Immunologic Factors / pharmacology*
  • Interleukin-6 / genetics
  • MAP Kinase Signaling System / drug effects*
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism*
  • NF-kappa B / metabolism*
  • Nitric Oxide / biosynthesis
  • Nitric Oxide Synthase Type II / genetics
  • Phagocytosis / drug effects
  • Polysaccharides / pharmacology*
  • RAW 264.7 Cells
  • Transcription Factor RelA / metabolism
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Immunologic Factors
  • Interleukin-6
  • NF-kappa B
  • Polysaccharides
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide
  • Nitric Oxide Synthase Type II
  • Mitogen-Activated Protein Kinases