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In vivo behavior of complete human oral mucosa equivalents: characterization in athymic mice
Author(s) -
Peña I.,
Junquera L. M.,
Meana Á.,
García E.,
Aguilar C.,
Fresno M. F.
Publication year - 2011
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.2010.01330.x
Subject(s) - cytokeratin , oral mucosa , vimentin , in vivo , pathology , basal (medicine) , immunohistochemistry , biology , chemistry , medicine , endocrinology , microbiology and biotechnology , insulin
Peña I, Junquera LM, Meana Á, García E, Aguilar C, Fresno MF. In vivo behavior of complete human oral mucosa equivalents: characterization in athymic mice. J Periodont Res 2011; 46: 214–220. © 2010 John Wiley & Sons A/S Background and Objective: The interest in tissue engineering as a way to achieve repair of damaged body tissues has led to the carrying out of many studies whose results point to the potential effectiveness of these methods. In a previous study, we reported the obtaining of complete autologous oral mucosa equivalents (CAOMEs), characterized by oral immature keratinocytes and stem cells on an autologous plasma and fibroblast scaffold. The purpose of this study is to show their behavior in vivo , by using them as free grafts in experimental animals, and to demonstrate their potential capacity to regenerate oral mucosa. Material and Methods: We engineered CAOMEs, as previously described. All CAOMEs thus obtained were used as free grafts in nu / nu mice. To assess their evolution in vivo , we studied their histological and immunohistochemical features by using AE1/AE3 pancytokeratin, the 5/6 cytokeratin pair, cytokeratin 13, laminin 5, collagen IV, vimentin, p‐63 and Ki‐67, at 7, 14 and 21 d. Results: The structure became progressively closer to that of oral mucosa samples. Cytokeratin 5/6 staining became increasingly intense in the basal and suprabasal layers, and cytokeratin 13 was exclusively positive in the superficial layers. The basal membrane was completed in 21 d. Vimentin showed a correct formation of the chorion. The increasingly positive staining of p‐63 and Ki‐67 indicated that the regeneration process was taking place. Conclusion: The present study shows the potential regenerative capacity of the CAOMEs by their ability to reach maturity similar to that seen in oral mucosa.