Inhibitory effect of GMI, an immunomodulatory protein from Ganoderma microsporum, on myofibroblast activity and proinflammatory cytokines in human fibrotic buccal mucosal fibroblasts

Environ Toxicol. 2018 Jan;33(1):32-40. doi: 10.1002/tox.22489. Epub 2017 Oct 6.

Abstract

Oral submucous fibrosis (OSF) has been indicated as one of the oral potentially malignant disorders. Epidemiological studies have attributed this pathological fibrosis to the habit of areca nuts chewing, which causes chronic inflammation and persistent activation of myofibroblasts in the oral cavity. Hence, it is crucial to find an effective intervention to ameliorate inflammation in order to prevent the malignant progression of OSF. In this study, we assessed the anti-inflammatory effect of the immunomodulatory protein, GMI, extracted from Ganoderma microsporum on the expression proinflammatory cytokines and the myofibroblast characteristics in human fibrotic buccal mucosal fibroblasts (fBMFs). Our results demonstrated that the expression level of interleukin (IL)-6 and IL-8 were decreased after exposure of GMI and the myofibroblast activities, including collagen gel contraction, migration, invasion, and wound healing abilities were inhibited as well. Furthermore, we confirmed these findings in the arecoline-stimulated BMFs. Consistent with the above findings, the expression of the myofibroblast marker α-smooth muscle actin and other fibrogenic markers, such as type I collagen, fibronectin, and vimentin in fBMFs were all reduced in a dose-dependent manner. Collectively, our data suggested that GMI suppressed the proinflammatory cytokines and myofibroblast features in fBMFs, and could serve as a promising and natural antifibrosis agent.

Keywords: GMI; arecoline; myofibroblast; oral submucous fibrosis.

MeSH terms

  • Actins / metabolism
  • Arecoline / pharmacology
  • Cell Movement / drug effects
  • Cells, Cultured
  • Collagen Type I / metabolism
  • Cytokines / metabolism*
  • Down-Regulation / drug effects
  • Enzyme-Linked Immunosorbent Assay
  • Fibroblasts / cytology
  • Fibroblasts / drug effects*
  • Fibroblasts / metabolism
  • Fibronectins / metabolism
  • Fungal Proteins / pharmacology*
  • Ganoderma / metabolism*
  • Humans
  • Interleukin-6 / analysis
  • Interleukin-6 / metabolism
  • Interleukin-8 / analysis
  • Interleukin-8 / metabolism
  • Mouth Mucosa / cytology
  • Oral Submucous Fibrosis / metabolism
  • Oral Submucous Fibrosis / pathology
  • Vimentin / metabolism

Substances

  • ACTA2 protein, human
  • Actins
  • Collagen Type I
  • Cytokines
  • Fibronectins
  • Fungal Proteins
  • Interleukin-6
  • Interleukin-8
  • Vimentin
  • Arecoline