GLM, a novel luteolin derivative, attenuates inflammatory responses in dendritic cells: Therapeutic potential against ulcerative colitis

Biochem Biophys Res Commun. 2019 Oct 8;518(1):87-93. doi: 10.1016/j.bbrc.2019.08.012. Epub 2019 Aug 9.

Abstract

GLM, a luteolin derivative, shows anti-melanogenic effect via regulation of various signal molecules; however, it is unclear whether it also exerts anti-inflammatory effect. This study investigated the mechanisms of the anti-inflammatory effect of GLM on activated dendritic cells (DCs) to elucidate its therapeutic potential for ulcerative colitis. The anti-inflammatory effect of GLM was firstly investigated based on its effect on DCs maturation and T cells proliferation/activation. GLM treatment downregulated pro-inflammatory cytokine productions, surface molecule expression, and antigen-presenting ability for MHC-II complex in LPS-activated DCs. Importantly, anti-inflammatory effect induced by GLM treatment were independent of MAPK/NF-κB signaling pathways. Furthermore, DCs that were co-treated with LPS and GLM impaired the proliferation and activation of naïve CD4+ T cells. Interestingly, GLM exerted in vivo protective effect in DSS-induced colitis models by decreasing Th1, Th2, and Th17 cells and myeloperoxidase (MPO) levels, as well as restoring body weight, disease activity, and DSS-induced pathology. Based on these results, GLM was shown to be a potential candidate treatment for ulcerative colitis.

Keywords: Anti-inflammatory activity; Dendritic cells; GLM; Ulcerative colitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation / drug effects
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cell Proliferation / drug effects
  • Colitis, Ulcerative / complications
  • Colitis, Ulcerative / drug therapy*
  • Colitis, Ulcerative / pathology*
  • Cytokines / biosynthesis
  • Dendritic Cells / drug effects
  • Dendritic Cells / pathology*
  • Dextran Sulfate
  • Female
  • Inflammation / complications
  • Inflammation / drug therapy*
  • Inflammation / pathology*
  • Lipopolysaccharides
  • Luteolin / chemistry
  • Luteolin / pharmacology
  • Luteolin / therapeutic use*
  • Lymphocyte Activation / drug effects
  • MAP Kinase Signaling System / drug effects
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Phenotype
  • Transcription Factor RelA / metabolism

Substances

  • Cytokines
  • Lipopolysaccharides
  • Transcription Factor RelA
  • Dextran Sulfate
  • Luteolin