Reconstruction of a full-thickness collagen-based human oral mucosal equivalent

被引:59
作者
Kinikoglu, Beste [1 ,2 ]
Auxenfans, Celine [1 ]
Pierrillas, Pascal [1 ,3 ]
Justin, Virginie [1 ]
Breton, Pierre [3 ]
Burillon, Carole [4 ]
Hasirci, Vasif [2 ]
Damour, Odile [1 ]
机构
[1] Hosp Civils Lyon, Banque Tissus & Cellules, F-69437 Lyon 03, France
[2] Middle E Tech Univ, BIOMAT, Dept Biotechnol, TR-06531 Ankara, Turkey
[3] Hosp Civils Lyon, Serv Chirurg Maxillofaciale, F-69495 Lyon, France
[4] Hosp Civils Lyon, Serv Ophtalmol, F-69437 Lyon, France
关键词
Oral mucosa engineering; Collagen scaffold; 3-D model; Oral fibroblasts; Oral epithelial cells; IN-VITRO; EX-VIVO; TISSUE; SKIN; MODEL;
D O I
10.1016/j.biomaterials.2009.08.010
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Tissue engineered human oral mucosa has the potential to be applied to the closure of surgical wounds after tissue deficits due to facial trauma, malignant lesion surgery or preposthetic procedure. It can also be used to elucidate the biology and pathology of oral mucosa and as a model alternative to animals for safety testing of oral care products. Using the technology previously developed in our laboratory for the production of a skin equivalent, we were able to reconstruct a nonkeratinized full-thickness human oral mucosal equivalent closely mimicking human native oral mucosa. The successive coculture of human lamina propria fibroblasts and human oral epithelial cells isolated from the nonkeratinized region of oral cavity in a porous collagen-glycosaminoglycan (GAG)-chitosan scaffold gave rise to a lamina propria equivalent (LPE) and then to an oral mucosa equivalent (OME). The results of the histology, immunohistology and transmission electron microscopy of this OME demonstrated the presence of a nonkeratinized pluristratified and differentiated epithelium as in native nonkeratinized human oral mucosa expressing both K13 and K3/76. This epithelium was firmly anchored to the LPE by a continuous and ultrastructurally well-organized basement membrane. In the LPE, fibroblasts synthesized new extracellular matrix where the average collagen fibre diameter was 28.4 nm, close to that of native oral mucosa. The proliferative capacity of the basal cells was demonstrated by the expression of Ki67. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6418 / 6425
页数:8
相关论文
共 35 条
[1]
Time-course study of histological and genetic patterns of differentiation in human engineered oral mucosa [J].
Alaminos, M. ;
Garzon, I. ;
Sanchez-Quevedo, M. C. ;
Moreu, G. ;
Gonzalez-Andrades, M. ;
Fernandez-Montoya, A. ;
Campos, A. .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2007, 1 (05) :350-359
[2]
Measurements of the protective effect of topically applied sunscreens using in vitro three-dimensional dermal and skin equivalents [J].
Augustin, C ;
Collombel, C ;
Damour, O .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 66 (06) :853-859
[3]
AUGUSTIN C, 1997, IN VITRO TOXICOL, V1, P21
[4]
Development of a hemicornea from human primary cell cultures for pharmacotoxicology testing [J].
Builles, N. ;
Bechetoille, N. ;
Justin, V. ;
Andre, V. ;
Barbaro, V. ;
Di Iorio, E. ;
Auxenfans, C. ;
Hulmes, D. J. S. ;
Damour, O. .
CELL BIOLOGY AND TOXICOLOGY, 2007, 23 (04) :279-292
[5]
Collombel C, 1987, French patent, Patent No. 8708252
[6]
COLLOMBEL C, 1989, Patent No. 8800303
[7]
Collombel C, 1987, European patent, Patent No. 884101948
[8]
Role of tissue engineering in oral and maxillofacial reconstruction: Findings of the 2005 AAOMS Research Summit [J].
Feinberg, SE ;
Aghaloo, TL ;
Cunningham, LL .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2005, 63 (10) :1418-1425
[9]
Gallico G G, 1995, Tissue Eng, V1, P231, DOI 10.1089/ten.1995.1.231
[10]
Status and potential commercial impact of stem cell-based treatments on dental and craniofacial regeneration [J].
Garcia-Godoy, Franklin ;
Murray, Peter E. .
STEM CELLS AND DEVELOPMENT, 2006, 15 (06) :881-887