dPGS Regulates the Phenotype of Macrophages via Metabolic Switching

Macromol Biosci. 2019 Dec;19(12):e1900184. doi: 10.1002/mabi.201900184. Epub 2019 Oct 21.

Abstract

The synthetic compound dendritic polyglycerol sulfate (dPGS) is a pleiotropic acting molecule but shows a high binding affinity to immunological active molecules as L-/P-selectin or complement proteins leading to well described anti-inflammatory properties in various mouse models. In order to make a comprehensive evaluation of the direct effect on the innate immune system, macrophage polarization is analyzed in the presence of dPGS on a phenotypic but also metabolic level. dPGS administered macrophages show a significant increase of MCP1 production paralleled by a reduction of IL-10 secretion. Metabolic analysis reveals that dPGS could potently enhance the glycolysis and mitochondrial respiration in M0 macrophages as well as decrease the mitochondrial respiration of M2 macrophages. In summary the data indicate that dPGS polarizes macrophages into a pro-inflammatory phenotype in a metabolic pathway-dependent manner.

Keywords: MCP1; infection; macrophage polarization; metabolic switch; polyglycerol sulfates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / immunology
  • Dendrimers / chemical synthesis
  • Dendrimers / pharmacology*
  • Gene Expression Regulation / drug effects*
  • Gene Expression Regulation / immunology
  • Glycerol / chemistry
  • Glycolysis / drug effects*
  • Glycolysis / genetics
  • Immunity, Innate
  • Immunophenotyping
  • Interleukin-10 / genetics
  • Interleukin-10 / immunology
  • Lectins / genetics
  • Lectins / immunology
  • Lectins, C-Type / genetics
  • Lectins, C-Type / immunology
  • Macrophage Colony-Stimulating Factor / pharmacology
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mitochondria / drug effects
  • Mitochondria / immunology
  • Mitochondria / metabolism
  • Oxidative Phosphorylation / drug effects*
  • Phenotype
  • Polymers / chemistry
  • Primary Cell Culture
  • Pyridines / chemistry
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology
  • beta-N-Acetylhexosaminidases / genetics
  • beta-N-Acetylhexosaminidases / immunology

Substances

  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Dendrimers
  • IL10 protein, mouse
  • Lectins
  • Lectins, C-Type
  • MGL2 protein, mouse
  • Polymers
  • Pyridines
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • polyglycerol
  • Macrophage Colony-Stimulating Factor
  • Chil3 protein, mouse
  • beta-N-Acetylhexosaminidases
  • Glycerol