Crucial effects of fibroblasts and keratinocyte growth factor on morphogenesis of reconstituted human oral epithelium

被引:77
作者
Costea, DE
Loro, LL
Dimba, EAO
Vintermyr, OK
Johannessen, AC
机构
[1] Univ Bergen, Fac Dent, Dept Odontol Oral Pathol & Forens Odontol, Bergen, Norway
[2] Univ Bergen, Haukeland Univ Hosp, Gade Inst, Dept Pathol, Bergen, Norway
关键词
cell culture; cell differentiation; epithelium; keratinocytes;
D O I
10.1111/j.1523-1747.2003.12616.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The connective tissue is known to have a general supportive effect for the development of the overlying epithelium; however, the more specific effects of fibroblasts and the involvement of their product, keratinocyte growth factor, on oral epithelial morphogenesis have not yet been addressed. Therefore, the purpose of this study was to investigate the effects of fibroblasts and keratinocyte growth factor on human oral epithelial morphogenesis in vitro. Reconstituted human oral epithelium was generated from primary human oral keratinocytes and fibroblasts by use of an organotypic cell culture model in a defined medium. Addition of fibroblasts to the collagen biomatrix increased total epithelial thickness from 28.0+/-5.0 mum to 66.1+/-8.6 mum (p=0.028), and basal cell proliferation from 3.6+/-0.7% to 16.6+/-1.1% (p=0.025). Presence of fibroblasts profoundly influenced the pattern of epithelial differentiation, and induced a switch in the pattern of cell death, from a predominance of spontaneous cell death in the basal cell layer (from 4.7+/-0.6% to 1.8+/-0.3%, p=0.029) to a more prevalent cell death due to terminal differentiation in the suprabasal cell layer (from 4.0+/- 0.1% to 5.4+/-0.1%, p=0.034). Keratinocyte growth factor promoted epithelial growth, but did not significantly enhance epithelial differentiation, demonstrating that fibroblasts possess additional mechanisms to keratinocyte growth factor synthesis that can modulate differentiation of reconstituted human oral epithelium.
引用
收藏
页码:1479 / 1486
页数:8
相关论文
共 42 条
[11]  
GARLICK JA, 1994, LAB INVEST, V70, P916
[12]   THE FATE OF GENETICALLY MARKED HUMAN ORAL KERATINOCYTES IN-VITRO [J].
GARLICK, JA ;
TAICHMAN, LB .
ARCHIVES OF ORAL BIOLOGY, 1993, 38 (10) :903-910
[13]   Epidermal growth factor and keratinocyte growth factor differentially regulate epidermal migration, growth, and differentiation [J].
Gibbs, S ;
Pinto, ANS ;
Murli, S ;
Huber, M ;
Hohl, D ;
Ponec, M .
WOUND REPAIR AND REGENERATION, 2000, 8 (03) :192-203
[14]   Intrinsic regulation of differentiation markers in human epidermis, hard palate and buccal mucosa [J].
Gibbs, S ;
Ponec, M .
ARCHIVES OF ORAL BIOLOGY, 2000, 45 (02) :149-158
[15]   Oral fibroblasts produce more HGF and KGF than skin fibroblasts in response to co-culture with keratinocytes [J].
Gron, B ;
Stoltze, K ;
Andersson, A ;
Dabelsteen, E .
APMIS, 2002, 110 (12) :892-898
[16]   Blood-group-related carbohydrates are expressed in organotypic cultures of human skin and oral mucosa [J].
Gron, B ;
Andersson, A ;
Dabelsteen, E .
APMIS, 1999, 107 (08) :779-790
[17]  
HILL MW, 1989, CELL TISSUE RES, V255, P179
[18]   A rote for skin γδ T cells in wound repair [J].
Jameson, J ;
Ugarte, K ;
Chen, N ;
Yachi, P ;
Fuchs, E ;
Boismenu, R ;
Havran, WL .
SCIENCE, 2002, 296 (5568) :747-749
[19]   Non-viral liposomal keratinocyte growth factor (KGF) cDNA gene transfer improves dermal and epidermal regeneration through stimulation of epithelial and mesenchymal factors [J].
Jeschke, MG ;
Richter, G ;
Höfstädter, F ;
Herndon, DN ;
Perez-Polo, JR ;
Jauch, KW .
GENE THERAPY, 2002, 9 (16) :1065-1074
[20]  
Kim SW, 2001, J BIOMED MATER RES, V58, P108, DOI 10.1002/1097-4636(2001)58:1<108::AID-JBM160>3.0.CO