The fibroblast growth factor binding protein is a novel interaction partner of FGF-7, FGF-10 and FGF-22 and regulates FGF activity: implications for epithelial repair

被引:80
作者
Beer, HD
Bittner, M
Niklaus, G
Munding, C
Max, N
Goppelt, A
Werner, S [1 ]
机构
[1] ETH Honggerberg, Inst Cell Biol, Dept Biol, CH-8093 Zurich, Switzerland
[2] Switch Biotech AG, D-82061 Neuried, Germany
关键词
epidermis; heparin; KGF; skin; wound;
D O I
10.1038/sj.onc.1208560
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The fibroblast growth factor-binding protein (FGF-BP) binds and activates FGF-1 and FGF-2, thereby contributing to tumor angiogenesis. In this study, we identified novel binding partners of FGF-BP, and we provide evidence for a role of this protein in epithelial repair processes. We show that expression of FGF-BP increases after injury to murine and human skin, in particular in keratinocytes. This upregulation is most likely achieved by major keratinocyte mitogens present at the wound site. Most importantly, we demonstrate that FGF-BP interacts with FGF-7, FGF-10, and with the recently identified FGF-22, and enhances the activity of low concentrations of ligand. Due to the important functions of FGF-7 and FGF-10 for repair of injured epithelia, our findings suggest that upregulation of FGF-BP expression after injury stimulates FGF activity at the wound site, thus enhancing the process of epithelial repair.
引用
收藏
页码:5269 / 5277
页数:9
相关论文
共 45 条
[1]   Tissue distribution and retinoid-mediated downregulation of an FGF-binding protein (FGF-BP) in the rat [J].
Aigner, A ;
Malerczyk, C ;
Houghtling, R ;
Wellstein, A .
GROWTH FACTORS, 2000, 18 (01) :51-+
[2]   Ribozyme-targeting of a secreted FGF-binding protein (FGF-BP) inhibits proliferation of prostate cancer cells in vitro and in vivo [J].
Aigner, A ;
Renneberg, H ;
Bojunga, J ;
Apel, J ;
Nelson, PS ;
Czubayko, F .
ONCOGENE, 2002, 21 (37) :5733-5742
[3]   Immunolocalization of an FGF-binding protein reveals a widespread expression pattern during different stages of mouse embryo development [J].
Aigner, A ;
Ray, PE ;
Czubayko, F ;
Wellstein, A .
HISTOCHEMISTRY AND CELL BIOLOGY, 2002, 117 (01) :1-11
[4]  
Aigner A, 2001, INT J CANCER, V92, P510, DOI 10.1002/1097-0215(20010515)92:4<510::AID-IJC1227>3.0.CO
[5]  
2-H
[6]   Mouse fibroblast growth factor 10: cDNA cloning, protein characterization, and regulation of mRNA expression [J].
Beer, HD ;
Florence, C ;
Dammeier, J ;
McGuire, L ;
Werner, S ;
Duan, DR .
ONCOGENE, 1997, 15 (18) :2211-2218
[7]   Fibroblast growth factor 22 and its potential role during skin development and repair [J].
Beyer, TA ;
Werner, S ;
Dickson, C ;
Grose, R .
EXPERIMENTAL CELL RESEARCH, 2003, 287 (02) :228-236
[8]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[9]  
BRAUCHLE M, 1994, ONCOGENE, V9, P3199
[10]   Protection of the intestinal mucosa by intraepithelial γδ T cells [J].
Chen, YP ;
Chou, K ;
Fuchs, E ;
Havran, WL ;
Boismenu, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (22) :14338-14343