Species-specific fibroblasts required for triggering invasiveness of partially transformed oral keratinocytes

被引:29
作者
Costea, Daniela Elena [1 ]
Kulasekara, Keerthi
Neppelberg, Evelyn
Johannessen, Anne Christine
Vintermyr, Olav Karsten
机构
[1] Univ Bergen, Dept Odontol, Gade Inst, Haukeland Univ Hosp, N-5021 Bergen, Norway
[2] Univ Bergen, Dept Oral Pathol & Forens, Gade Inst, Haukeland Univ Hosp, N-5021 Bergen, Norway
[3] Univ Bergen, Dept Oral Surg, Gade Inst, Haukeland Univ Hosp, N-5021 Bergen, Norway
[4] Univ Bergen, Dept Oral Med, Gade Inst, Haukeland Univ Hosp, N-5021 Bergen, Norway
[5] Univ Bergen, Dept Pathol, Gade Inst, Haukeland Univ Hosp, N-5021 Bergen, Norway
关键词
D O I
10.2353/ajpath.2006.050843
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
This study tests the hypothesis that invasion of partially transformed keratinocytes is initiated by diffusible, proinvasive signals provided by species-specific fibroblasts. In vitro organotypic cultures of neoplastic human oral mucosa were constructed by growing a partially transformed, nontumorigenic keratinocytic cell line isolated from a dysplastic human oral lesion (DOK-ECACC94122104) on top of various types of connective tissue equivalents. Cultured tissues were analyzed by histomorphometry (depth and area of invasion: D-inv, A(inv)) and immunohistochemistry. Presence of human fibroblasts in the matrix induced a local invasion of DOK (D-inv = 95.6 +/- 7.1 mu m, A(inv) = 45.8 +/- 3.5%). Minimal invasion (P < 0.05) was observed when DOK grew on simple collagen matrix (D-inv 14.1 +/- 2.1 mu m, A(inv) = 3.7 +/- 0.8%) or matrices containing fibroblasts from mouse (D-inv = 11.5 +/- 4.0 mu m, A(inv) = 4.3 +/- 1.0%) or rat (D-inv = 15.6 +/- 1.2 mu m, A(inv) = 6.1 +/- 0.5%). In these cultures, local invasion could be induced by the presence of human fibroblasts in a bottom layer of the collagen matrix (P < 0.05) or by conditioned medium from organotypic cultures of DOK on human fibroblast-containing matrix (P < 0.05) but not by conditioned medium from human fibroblast monocultures (P > 0.05). Deposition of human collagen IV was observed at epithelial-matrix interface only when DOK behaved invasively. in conclusion, invasion of partially transformed oral keratinocytes was triggered by keratinocyte-induced fibroblast-derived diffusible factor(s) in a species-specific manner and associated with de novo synthesis of collagen TV.
引用
收藏
页码:1889 / 1897
页数:9
相关论文
共 46 条
[1]   Microenvironmental control of premalignant disease: the role of intercellular adhesion in the progression of squamous cell carcinoma [J].
Alt-Holland, A ;
Zhang, WT ;
Margulis, A ;
Garlick, JA .
SEMINARS IN CANCER BIOLOGY, 2005, 15 (02) :84-96
[2]   Basement membrane proteins promote progression of intraepithelial neoplasia in 3-dimensional models of human stratified epithelium [J].
Andriani, F ;
Garfield, J ;
Fusenig, NE ;
Garlick, JA .
INTERNATIONAL JOURNAL OF CANCER, 2004, 108 (03) :348-357
[3]   Fibroblasts can modulate the phenotype of malignant epithelial cells in vitro [J].
Atula, S ;
Grenman, R ;
Syrjanen, S .
EXPERIMENTAL CELL RESEARCH, 1997, 235 (01) :180-187
[4]   Stromagenesis: The changing face of fibroblastic microenvironments during tumor progression [J].
Beacham, DA ;
Cukierman, E .
SEMINARS IN CANCER BIOLOGY, 2005, 15 (05) :329-341
[5]   3-dimensional in vitro invasion model for oral squamous epithelial carcinomas. Evaluation of tumor and stromal cell properties as well as extracellular matrix [Dreidimensionales In-vitro-Invasionsmodell für orale Plattenepithelkarzinome. Evaluation von Tumor- und Stromazelleigenschaften sowie der extrazellulären Matrix.] [J].
Berndt A. ;
Hyckel P. ;
Könneker A. ;
Kosmehl H. .
Mund-, Kiefer- und Gesichtschirurgie, 1998, 2 (5) :256-260
[6]  
Berndt A, 1997, INVAS METAST, V17, P251
[7]   Fibrillary co-deposition of laminin-5 and large unspliced tenascin-C in the invasive front of oral squamous cell carcinoma in vivo and in vitro [J].
Berndt, A ;
Borsi, L ;
Hyckel, P ;
Kosmehl, H .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2001, 127 (05) :286-292
[8]   Stromal fibroblasts in cancer initiation and progression [J].
Bhowmick, NA ;
Neilson, EG ;
Moses, HL .
NATURE, 2004, 432 (7015) :332-337
[9]  
Breuninger H, 1997, CANCER-AM CANCER SOC, V79, P915, DOI 10.1002/(SICI)1097-0142(19970301)79:5<915::AID-CNCR7>3.0.CO
[10]  
2-A