Mouse fibroblast growth factor 10: cDNA cloning, protein characterization, and regulation of mRNA expression

被引:108
作者
Beer, HD
Florence, C
Dammeier, J
McGuire, L
Werner, S
Duan, DR
机构
[1] HUMAN GENOME SCI INC,ROCKVILLE,MD 20850
[2] MAX PLANCK INST BIOCHEM,D-82152 MARTINSRIED,GERMANY
关键词
keratinocyte growth factor; secretion; wound repair; heparin; growth factor; regulation;
D O I
10.1038/sj.onc.1201383
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
Fibroblast growth factor 7 (FGF-7) or keratinocyte growth factor (KGF), is a potent and specific mitogen for epithelial cells, We have recently identified a novel human FGF-7 homologue, named FGF-10. To study the expression of this new FGF family member and its regulation in wound repair, we cloned the mouse FGF-10 (mFGF-10) cDNA, The encoded protein is 92% identical to human FGF-10 and 91% identical to rat FGF-10, When expressed in mammalian 293 cells, the mFGF-10 protein was glycosylated but remained cell- or extracellular matrix-associated. Upon addition of heparin, mFGF-10 protein was released into the media, mRNA encoding mFGF-10 was relatively abundant in lung, skin, brain and heart, In the skin, both FGF-7 and mFGF-10 were expressed in the dermal, but not the epidermal compartment, In contrast to FGF-7, mFGF-10 expression was not induced during cutaneous wound repair, In cultured fibroblasts, expression of mFGF-10 was strongly repressed by transforming growth factor beta and tumor necrosis factor alpha, whereas epidermal growth factor and interleukin-1 beta had no effect, These results demonstrate a differential regulation of mFGF-10 and FGF-7 expression in vitro and during the wound healing process.
引用
收藏
页码:2211 / 2218
页数:8
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