Time-course study of histological and genetic patterns of differentiation in human engineered oral mucosa

被引:34
作者
Alaminos, M. [1 ,2 ,3 ]
Garzon, I. [1 ]
Sanchez-Quevedo, M. C. [1 ]
Moreu, G. [4 ]
Gonzalez-Andrades, M. [1 ]
Fernandez-Montoya, A. [1 ,5 ]
Campos, A. [1 ]
机构
[1] Univ Granada, Dept Histol, E-18012 Granada, Spain
[2] Fdn FIBAO, Granada, Spain
[3] Univ Hosp San Cecilio, Granada, Spain
[4] Univ Granada, Dept Stomatol, E-18012 Granada, Spain
[5] Transfus Ctr & Tissue Bank Granada CRTS, Granada, Spain
关键词
tissue engineering; oral mucosa; histodifferentiation; microarray; electron microscopy; development;
D O I
10.1002/term.38
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The lack of sufficient oral mucosa available for intra-oral grafting is a major surgical problem, and new sources of oral tissues for clinical use are needed. In this regard, some models of engineered oral mucosa have been reported to date, but little is known about the structural and genetic mechanisms that occur during the process of development and maturation of these tissue substitutes. We have carried out a time-course study of the genes and morphological patterns of cell and tissue differentiation that develop in oral mucosa constructs after 3, 7, 11 and 21 days of development. Our electron microscopy and microarray analyses demonstrated that the oral mucosa constructs generated by tissue engineering undergo a progressive process of cell differentiation with the sequential formation and maturation of several layers of epithelium (with expression of stratifin, sciellin, involucrin, trichohyalin and kallikrein 7), intercellular junctions (with expression of plakophilin, desmocollin, desmoglein and cadherins), cytokeratins, a basement membrane (laminins, collagen M and the extracellular matrix (biglycan, matrix metalloproteinases). In conclusion, although the level and type of keratinization developed in vitro could be different, the oral mucosa substitutes were very similar to the native tissues. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:350 / 359
页数:10
相关论文
共 48 条
[1]   Evaluation of the viability of cultured corneal endothelial cells by quantitative electron probe X-ray microanalysis [J].
Alaminos, M. ;
Sanchez-Quevedo, M. C. ;
Munoz-Avila, J. I. ;
Garcia, J. M. ;
Crespo, P. V. ;
Gonzalez-Andrades, M. ;
Campos, A. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 211 (03) :692-698
[2]  
Alaminos M, 2003, CANCER RES, V63, P4538
[3]   Construction of a complete rabbit cornea substitute using a fibrin-agarose scaffold [J].
Alaminos, Miguel ;
Del Carmen Sanchez-Quevdo, Maria ;
Munoz-Avila, Jose Ignacio ;
Serrano, Daniel ;
Medialdea, Santiago ;
Carreras, Ignacio ;
Campos, Antonio .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (08) :3311-3317
[4]   Tissue engineering of artificial organs [J].
Atala, A .
JOURNAL OF ENDOUROLOGY, 2000, 14 (01) :49-57
[5]   The differentiation profile of the epithelium of the human lip [J].
Barrett, AW ;
Morgan, M ;
Nwaeze, G ;
Kramer, G ;
Berkovitz, BKB .
ARCHIVES OF ORAL BIOLOGY, 2005, 50 (04) :431-438
[6]   Polycomb complexes repress developmental regulators in murine embryonic stem cells [J].
Boyer, LA ;
Plath, K ;
Zeitlinger, J ;
Brambrink, T ;
Medeiros, LA ;
Lee, TI ;
Levine, SS ;
Wernig, M ;
Tajonar, A ;
Ray, MK ;
Bell, GW ;
Otte, AP ;
Vidal, M ;
Gifford, DK ;
Young, RA ;
Jaenisch, R .
NATURE, 2006, 441 (7091) :349-353
[7]   Expression of the angiogenesis markers vascular endothelial growth factor-A, thrombospondin-1, and platelet-derived endothelial cell growth factor in human sporadic adrenocortical tumors: Correlation with genotypic alterations [J].
de Fraipont, F ;
El Atifi, M ;
Gicquel, C ;
Bertagna, X ;
Chambaz, EM ;
Feige, JJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (12) :4734-4741
[8]  
DOUROV N, 1984, SCANNING ELECTRON MI, V1, P243
[9]   Stratum corneum tryptic enzyme in normal epidermis: A missing link in the desquamation process? [J].
Ekholm, IE ;
Brattsand, M ;
Egelrud, T .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 114 (01) :56-63
[10]   CEA-related cell adhesion molecule 1:: A potent angiogenic factor and a major effector of vascular endothelial growth factor [J].
Ergün, S ;
Kilic, N ;
Ziegeler, G ;
Hansen, A ;
Nollau, P ;
Götze, J ;
Wurmbach, JH ;
Horst, A ;
Weil, J ;
Fernando, M ;
Wagener, C .
MOLECULAR CELL, 2000, 5 (02) :311-320