Activation of TGF-β pathway by areca nut constituents: a possible cause of oral submucous fibrosis

PLoS One. 2012;7(12):e51806. doi: 10.1371/journal.pone.0051806. Epub 2012 Dec 19.

Abstract

Oral submucous fibrosis (OSF) is a chronic inflammatory disease characterized by the accumulation of excess collagen, and areca nut chewing has been proposed as an important etiological factor for disease manifestation. Activation of transforming growth factor-β signaling has been postulated as the main causative event for increased collagen production in OSF. Oral epithelium plays important roles in OSF, and arecoline has been shown to induce TGF-β in epithelial cells. In an attempt to understand the role of areca nut constituents in the manifestation of OSF, we studied the global gene expression profile in epithelial cells (HaCaT) following treatment with areca nut water extract or TGF-β. Interestingly, 64% of the differentially regulated genes by areca nut water extract matches with the TGF-β induced gene expression profile. Out of these, expression of 57% of genes was compromised in the presence of ALK5 (TβRI) inhibitor and 7% were independently induced by areca nut, highlighting the importance of TGF-β in areca nut actions. Areca nut water extract treatment induced p-SMAD2 and TGF-β downstream targets in HaCaT cells but not in human gingival fibroblast cells (hGF), suggesting epithelial cells could be the source of TGF-β in promoting OSF. Water extract of areca nut consists of polyphenols and alkaloids. Both polyphenol and alkaloid fractions of areca nut were able to induce TGF-β signaling and its downstream targets. Also, SMAD-2 was phosphorylated following treatment of HaCaT cells by Catechin, Tannin and alkaloids namely Arecoline, Arecaidine and Guvacine. Moreover, both polyphenols and alkaloids induced TGF-β2 and THBS1 (activator of latent TGF-β) in HaCaT cells suggesting areca nut mediated activation of p-SMAD2 involves up-regulation and activation of TGF-β. These data suggest a major causative role for TGF-β that is induced by areca nut in OSF progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Areca / adverse effects*
  • Arecoline / analogs & derivatives*
  • Arecoline / pharmacology
  • Biomarkers / metabolism*
  • Cells, Cultured
  • Collagen / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Gene Expression Profiling
  • Gingiva / cytology
  • Gingiva / drug effects
  • Gingiva / metabolism
  • Humans
  • Keratinocytes / cytology
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • Mastication
  • Nuts / adverse effects*
  • Oligonucleotide Array Sequence Analysis
  • Oral Submucous Fibrosis / etiology*
  • Phosphorylation / drug effects
  • Plant Extracts / pharmacology
  • Plants, Toxic / adverse effects
  • RNA, Messenger / genetics
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Smad2 Protein / genetics
  • Smad2 Protein / metabolism*
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism*
  • Up-Regulation

Substances

  • Biomarkers
  • Plant Extracts
  • RNA, Messenger
  • SMAD2 protein, human
  • Smad2 Protein
  • Transforming Growth Factor beta
  • arecaidine
  • Arecoline
  • Collagen

Grants and funding

The authors acknowledge Department of Science and Technology (DST), Government of India, for funding this study and Infrastructural support from DST (Fund for Improvement of Science and Technology) and University Grants Commission, Government of India, to the Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science. IK is recipient of a fellowship from Council of Scientific and Industrial Research, New Delhi. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.