Gingival mucosa regeneration in athymic mice using in vitro engineered human oral mucosa.

Biomaterials

Groupe de Recherche en Ecologie Buccale, Faculté de médecine dentaire, Université Laval, Québec, Quebec G1K 7P4, Canada.

Published: August 2010

AI Article Synopsis

  • The study aimed to evaluate the effectiveness of engineered human oral mucosa for repairing mucosal defects in the oral cavity.
  • Human gingival cells combined with a collagen scaffold created a well-structured artificial mucosa that showed no wound contraction after grafting.
  • The regenerated tissue was similar to natural mucosa in terms of structure, layers, and blood supply, indicating a promising alternative for oral mucosal repair.

Article Abstract

Our goal was to investigate in vivo tissue formation following the grafting of engineered human oral mucosa to demonstrate its usefulness in replacing mucosal defects in the oral cavity. Human gingival cells were isolated from the oral mucosa and were used in combination with a collagen scaffold to engineer oral mucosa. Structural and ultrastructural analyses revealed that the engineered mucosa had a well-organized stratified epithelium on the surface of the fibroblast-populated lamina propria tissue. Following grafting for 15 and 60 days, the engineered oral mucosa was shown to cover the recipient site with no wound contraction. The regenerated mucosa displayed an epithelium with multiple layers, including a stratum corneum where epithelial cells expressed cytokeratin Ki-67 and K-14 positive cells located in the basal and supra-basal layers. The interaction between the epithelium and the lamina propria was promoted by the formation of a basement membrane structure containing key proteins, such as laminin-5 and type IV collagen. Following the engineered mucosa grafting, the regenerated tissue was well vascularized, similar to the native mucosa. These data demonstrate the usefulness of engineered human oral mucosa as an alternative treatment for mucosal defects in the oral cavity.

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Source
http://dx.doi.org/10.1016/j.biomaterials.2010.04.004DOI Listing

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