Effects of C-xylopyranoside derivative on epithelial regeneration in an in vitro 3D oral mucosa model

Biosci Biotechnol Biochem. 2016 Jul;80(7):1344-55. doi: 10.1080/09168451.2016.1153957. Epub 2016 Mar 11.

Abstract

Identifying substandard tissue-engineered oral mucosa grafts with a poor epithelium before clinical use is critical to ensure quality assurance/control in regenerative medicine, leading to success of grafting. This study investigated the effects of one of the C-xylopyranoside derivatives, β-D-xylopyranoside-n-propane-2-one (XPP), on oral epithelial regeneration. Using a three-dimensional oral mucosa model, we analyzed changes of the epithelial structure, glycosaminoglycan (GAG) synthesis, the expression levels of basement membrane zone markers, and substrates of Akt/mTOR signaling. Compared with the control, 2 mM XPP treatment increased the mean and minimal epithelial thickness, and reduced the variation of epithelial thickness. It also stimulated expressions of decorin and syndecan-1 with change of GAG amount and/or composition, and enhanced the expressions of integrin α6, CD44, and Akt/mTOR signaling substrates. These findings suggest that XPP supplementation contributes to consistent epithelial regeneration. Moreover, upregulation of those markers may play a role in increasing the quality of the oral mucosal epithelium.

Keywords: epithelium; glycosaminoglycan; in vitro model; oral mucosa; regenerative medicine.

MeSH terms

  • Basement Membrane / drug effects
  • Basement Membrane / metabolism
  • Decorin / genetics
  • Decorin / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / drug effects*
  • Fibroblasts / metabolism
  • Gene Expression Regulation
  • Glycosaminoglycans / agonists
  • Glycosaminoglycans / biosynthesis*
  • Glycosides / pharmacology*
  • Humans
  • Hyaluronan Receptors
  • Integrin alpha6 / genetics
  • Integrin alpha6 / metabolism
  • Keratinocytes / cytology
  • Keratinocytes / drug effects*
  • Keratinocytes / metabolism
  • Models, Biological
  • Mouth Mucosa / cytology
  • Mouth Mucosa / drug effects*
  • Mouth Mucosa / metabolism
  • Primary Cell Culture
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Regeneration / drug effects*
  • Regeneration / genetics
  • Signal Transduction
  • Syndecan-1 / genetics
  • Syndecan-1 / metabolism
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism
  • Tissue Engineering

Substances

  • CD44S antigen
  • DCN protein, human
  • Decorin
  • Glycosaminoglycans
  • Glycosides
  • Hyaluronan Receptors
  • Integrin alpha6
  • SDC1 protein, human
  • Syndecan-1
  • MTOR protein, human
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases