FGF signals for cell proliferation and migration through different pathways

被引:257
作者
Boilly, B
Vercoutter-Edouart, AS
Hondermarck, H
Nurcombe, V
Le Bourhis, X
机构
[1] Univ Sci & Technol Lille, Equipe Facteurs Croissance, UPRES 1033, F-59655 Villeneuve Dascq, France
[2] Univ Queensland, Dept Anat Sci, St Lucia, Qld 4072, Australia
关键词
FGF; receptor; signaling pathway; migration; proliferation;
D O I
10.1016/S1359-6101(00)00014-9
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
FGFs are pleiotropic growth factors that control cell proliferation, migration and differentiation. However, FGF transduction studies have so far focused primarily on the mitogenic effect of this growth factor family and it has been difficult to assess if the described intracellular signaling pathways are dedicated solely to cell proliferation, or whether they are equally important for the migratory activity often seen in responsive cells. We review here papers in which the migratory effects of this growth factor family were clearly discriminated from proliferative effects. In tote: these studies suggest that cells use different signaling pathways for migration, such as Src and p38 MAP kinase, from those for proliferation, which tend to upregulate the ERKs. which signaling pathway a cell uses for proliferation or migration appears to depend on many factors, including the structure and the quantity of available FGF trapped in the basal lamina by heparan sulfate co-factors, the disposition of cognate high affinity receptors and the general environment of the cell. Thus the density of the cell population, the state of the cell cycle, the presence of other factors or receptors will modulate the migratory response of cells to FGF. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 73 条
[1]   ASSAYS FOR ANGIOGENESIS - A REVIEW [J].
AUERBACH, R ;
AUERBACH, W ;
POLAKOWSKI, I .
PHARMACOLOGY & THERAPEUTICS, 1991, 51 (01) :1-11
[2]  
BATTEGAY EJ, 1995, J MOL MED, V73, P333
[3]   Heartless, a Drosophila FGF receptor homolog, is essential for cell migration and establishment of several mesodermal lineages [J].
Beiman, M ;
Shilo, BZ ;
Volk, T .
GENES & DEVELOPMENT, 1996, 10 (23) :2993-3002
[4]  
BESSER D, 1995, CELL GROWTH DIFFER, V6, P1009
[5]   DIFFERENTIAL MODULATION OF CELL PHENOTYPE BY DIFFERENT MOLECULAR-WEIGHT FORMS OF BASIC FIBROBLAST GROWTH-FACTOR - POSSIBLE INTRACELLULAR SIGNALING BY THE HIGH-MOLECULAR-WEIGHT FORMS [J].
BIKFALVI, A ;
KLEIN, S ;
PINTUCCI, G ;
QUARTO, N ;
MIGNATTI, P ;
RIFKIN, DB .
JOURNAL OF CELL BIOLOGY, 1995, 129 (01) :233-243
[6]   Control of cell migration during Caenorhabditis elegans development [J].
Blelloch, R ;
Newman, C ;
Kimble, J .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (05) :608-613
[7]  
Bonneton C, 1999, CELL MOTIL CYTOSKEL, V43, P288, DOI 10.1002/(SICI)1097-0169(1999)43:4<288::AID-CM2>3.3.CO
[8]  
2-P
[9]   CYCLIC-AMP DISTINGUISHES BETWEEN 2 FUNCTIONS OF ACIDIC FGF IN A RAT BLADDER-CARCINOMA CELL-LINE [J].
BOYER, B ;
THIERY, JP .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :767-776
[10]   REARRANGEMENTS OF DESMOSOMAL AND CYTOSKELETAL PROTEINS DURING THE TRANSITION FROM EPITHELIAL TO FIBROBLASTOID ORGANIZATION IN CULTURED RAT BLADDER-CARCINOMA CELLS [J].
BOYER, B ;
TUCKER, GC ;
VALLES, AM ;
FRANKE, WW ;
THIERY, JP .
JOURNAL OF CELL BIOLOGY, 1989, 109 (04) :1495-1509