Immunomodulatory Properties of Polysaccharides from the Coral Pseudopterogorgia americana in Macrophages

Cells. 2021 Dec 14;10(12):3531. doi: 10.3390/cells10123531.

Abstract

Polysaccharides from marine organisms produce an important regulatory effect on the mammalian immune system. In this study, the immunomodulatory properties of a polysaccharide that was isolated from the coral Pseudopterogorgia americana (PPA) were investigated. PPA increased the expression levels of tumour necrosis factor-α (TNF-α), interleukin-6 (IL-6) and cyclooxygenase-2 (COX-2), but not inducible nitric oxide synthase and nitric oxide, in macrophages. A mechanistic study revealed that PPA activated macrophages through the toll-like receptor-4 and induced the generation of reactive oxygen species (ROS), increased the phosphorylation levels of protein kinase C (PKC)-α, PKC-δ and mitogen-activated protein kinases (MAPK), and activated NF-κB. The inhibition of ROS and knockdown of PKC-α reduced PPA-mediated TNF-α and IL-6 expression; however, the knockdown of PKC-δ significantly increased PPA-mediated TNF-α expression. In addition, the inhibition of c-Jun N-terminal kinase-1/2 and NF-κB reduced PPA-mediated TNF-α, IL-6 and COX-2 expression. Furthermore, the inhibition of ROS, MAPK and PKC-α/δ reduced PPA-mediated NF-κB activation, indicating that ROS, MAPK and PKC-α/δ function as upstream signals of NF-κB. Finally, PPA treatment decreased the phagocytosis activity of macrophages and reduced cytokine expression in bacteria-infected macrophages. Taken together, our current findings suggest that PPA can potentially play a role in the development of immune modulators in the future.

Keywords: Pseudopterogorgia americana; immune modulation; macrophages; polysaccharide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anthozoa / chemistry*
  • Cyclooxygenase 2 / metabolism
  • Cytokines / biosynthesis
  • Escherichia coli / drug effects
  • Escherichia coli / physiology
  • Humans
  • Immunologic Factors / pharmacology*
  • Inflammation Mediators / metabolism
  • Interleukin-6 / metabolism
  • Lipopolysaccharides
  • Macrophage Activation / drug effects
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Macrophages / microbiology
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Phagocytosis / drug effects
  • Polysaccharides / chemistry
  • Polysaccharides / pharmacology*
  • Protein Kinase C-alpha / metabolism
  • Protein Kinase C-delta / metabolism
  • RAW 264.7 Cells
  • Reactive Oxygen Species / metabolism
  • THP-1 Cells
  • Toll-Like Receptor 4 / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Immunologic Factors
  • Inflammation Mediators
  • Interleukin-6
  • Lipopolysaccharides
  • NF-kappa B
  • Polysaccharides
  • Reactive Oxygen Species
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Cyclooxygenase 2
  • Protein Kinase C-alpha
  • Protein Kinase C-delta
  • Mitogen-Activated Protein Kinases