Characterization of Multilayered Tissue-Engineered Human Alveolar Bone and Gingival Mucosa

Tissue Eng Part C Methods. 2018 Feb;24(2):99-107. doi: 10.1089/ten.TEC.2017.0370. Epub 2018 Jan 10.

Abstract

Advances in tissue engineering have permitted assembly of multilayered composite tissue constructs for potential applications in the treatment of combined hard and soft tissue defects and as an alternative in vitro test model to animal experimental systems. The aim of this study was to develop and characterize a novel three-dimensional combined human alveolar bone and gingival mucosal model based on primary cells isolated from the oral tissues. Bone component of the model was engineered by seeding primary human alveolar osteoblasts into a hydroxyapatite/tricalcium phosphate scaffold and culturing in a spinner bioreactor. The engineered bone was then laminated, using an adhesive tissue sealant, with tissue-engineered gingival mucosa consisting of air/liquid interface-cultured normal human gingival keratinocytes on oral fibroblast-populated collagen gel scaffold. Histological characterization revealed a structure consisting of established epithelial, connective tissue and bone layers closely comparable to normal oral tissue architecture. The mucosal component demonstrated a mature epithelium undergoing terminal differentiation similar to that characteristic of native buccal mucosa, as confirmed using cytokeratin 13 and cytokeratin 14 immunohistochemistry. Ultrastructural analysis confirmed the presence of desmosomes and hemidesmosomes in the epithelial layer, a continuous basement membrane, and newly synthesized collagen in the connective tissue layer. Quantitative polymerase chain reaction (qPCR) assessment of osteogenesis-related gene expression showed a higher expression of genes encoded collagen I (COL1) and osteonectin (ON) compared with osteocalcin (OC), osteopontin (OP), and alkaline phosphatase (ALP). Enzyme-linked immunosorbent assay quantification of COL1, ON, and OC confirmed a pattern of secretion, which paralleled the model's gene expression profile. We demonstrate in this study that, replicating the anatomical setting between oral mucosa and the underlying alveolar bone is feasible and the developed model showed characteristics similar to those of normal tissue counterparts. This trilayered model therefore offers great scope as an advanced and anatomically representative tissue-engineered alternative to animal models.

Keywords: alveolar bone mucosal model; bone engineering; composite tissue engineering; oral mucosa engineering.

MeSH terms

  • Alveolar Process / cytology*
  • Alveolar Process / metabolism
  • Biomarkers / metabolism
  • Bone Regeneration*
  • Cells, Cultured
  • Fibroblasts / cytology*
  • Fibroblasts / metabolism
  • Gingiva / cytology*
  • Gingiva / metabolism
  • Humans
  • Mouth Mucosa / cytology*
  • Mouth Mucosa / metabolism
  • Osteoblasts / cytology*
  • Osteoblasts / metabolism
  • Tissue Engineering / methods*
  • Tissue Scaffolds

Substances

  • Biomarkers