In vitro and in vivo cytokeratin patterns of expression in bioengineered human periodontal mucosa

被引:48
作者
Garzon, I. [1 ]
Sanchez-Quevedo, M. C. [1 ]
Moreu, G. [2 ]
Gonzalez-Jaranay, M. [2 ]
Gonzalez-Andrades, M. [1 ]
Montalvo, A. [1 ]
Campos, A. [1 ]
Alaminos, M. [1 ]
机构
[1] Univ Granada, Dept Histol, Tissue Engn Grp, E-18012 Granada, Spain
[2] Univ Granada, Dept Stomatol, Unit Periodont, E-18012 Granada, Spain
关键词
oral mucosa; tissue engineering; cytokeratins; microarray; ENGINEERED ORAL-MUCOSA; IMMUNODEFICIENT MICE; ORGANOTYPIC CULTURE; GROWTH-FACTOR; FIBROBLASTS; CELLS; SKIN; DIFFERENTIATION; KERATINOCYTES; EQUIVALENT;
D O I
10.1111/j.1600-0765.2008.01159.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background and Objective: Development of human oral mucosa substitutes by tissue engineering may provide new therapeutic tools for the management of periodontal diseases. In this study we evaluated a fibrin-agarose human oral mucosa substitute both in vitro and in vivo. Material and Methods: In vitro bioengineered oral mucosa substitutes were developed from irrelevant biopsy samples of human oral gingiva. In vivo evaluation of the constructed tissues was performed by implantation into athymic nude mice. The expression of several epithelial markers was assessed by microarray analysis and immunohistochemistry. Results: Bioengineered oral mucosa samples kept in vitro developed a multilayered epithelium that expressed several cytokeratins, including some markers of simple epithelia (cytokeratins 7, 8 and 18), along with markers of stratified epithelia (cytokeratins 5 and 13) and of cell proliferation (proliferating cell nuclear antigen). Bioengineered tissues grafted in vivo onto nude mice exhibited very good biointegration with the host, showing a cytokeratin expression pattern that was very similar to that of normal native oral mucosa controls. Histological analysis of the artificial tissues demonstrated that oral mucosa substitutes evaluated in vivo were structurally mature, showing some typical structures of human native oral mucosa such as rete ridges and chorial papillae, along with numerous blood vessels at the fibrin-agarose stromal substitute. These structures were absent in samples evaluated in vitro. Conclusion: The results indicate that this model of human oral mucosa, constructed using fibrin-agarose scaffolds, shows similarities to native oral mucosa controls and imply that bioengineered oral mucosa substitutes could eventually be used clinically.
引用
收藏
页码:588 / 597
页数:10
相关论文
共 38 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]  
Albandar Jasim M, 2005, Dent Clin North Am, V49, P517, DOI 10.1016/j.cden.2005.03.003
[3]   Destructive periodontal disease in adults 30 years of age and older in the United states, 1988-1994 [J].
Albandar, JM ;
Brunelle, JA ;
Kingman, A .
JOURNAL OF PERIODONTOLOGY, 1999, 70 (01) :13-29
[4]   Platelet-derived growth factor gene delivery stimulates ex vivo gingival repair [J].
Anusaksathien, O ;
Webb, SA ;
Jin, QM ;
Giannobile, WV .
TISSUE ENGINEERING, 2003, 9 (04) :745-756
[5]   Recapitulation of oral mucosal tissues in long-term organotypic culture [J].
Chinnathambi, S ;
Tomanek-Chalkley, A ;
Ludwig, N ;
King, E ;
DeWaard, R ;
Johnson, G ;
Wertz, PW ;
Bickenach, JR .
ANATOMICAL RECORD PART A-DISCOVERIES IN MOLECULAR CELLULAR AND EVOLUTIONARY BIOLOGY, 2003, 270A (02) :162-174
[6]   Crucial effects of fibroblasts and keratinocyte growth factor on morphogenesis of reconstituted human oral epithelium [J].
Costea, DE ;
Loro, LL ;
Dimba, EAO ;
Vintermyr, OK ;
Johannessen, AC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (06) :1479-1486
[7]  
DALE B A, 1990, Critical Reviews in Oral Biology and Medicine, V1, P167
[8]   Gene-enhanced tissue engineering for dental hard tissue regeneration: (2) dentin-pulp and periodontal regeneration [J].
Paul C Edwards ;
James M Mason .
Head & Face Medicine, 2 (1)
[9]   Expression of keratins in normal, immortalized and malignant oral epithelia in organotypic culture [J].
Hansson, A ;
Bloor, BK ;
Haig, Y ;
Morgan, PR ;
Ekstrand, J ;
Grafström, RC .
ORAL ONCOLOGY, 2001, 37 (05) :419-430
[10]   Cultured mucosal cell sheet with a double layer of keratinocytes and fibroblasts on a collagen membrane [J].
Imaizumi, F ;
Asahina, I ;
Moriyama, T ;
Ishii, M ;
Omura, K .
TISSUE ENGINEERING, 2004, 10 (5-6) :657-664