Flaumenhaft R, Moscatelli D, Rifkin D B
Department of Cell Biology and Kaplan Cancer Center, New York University Medical Center, New York.
J Cell Biol. 1990 Oct;111(4):1651-9. doi: 10.1083/jcb.111.4.1651.
The radius of diffusion of basic FGF (bFGF) in the presence and in the absence of the glycosaminoglycans heparin and heparan sulfate was measured. Iodinated 125I-bFGF diffuses further in agarose, fibrin, and on a monolayer of bovine aortic endothelial (BAE) cells in the presence of heparin than in its absence. Heparan sulfates affected the diffusion of 125I-bFGF in a manner similar to, though less pronounced than, heparin. When applied at the center of a monolayer of BAE cells, bFGF plus heparin stimulated morphological changes at a 10-fold greater radius than bFGF alone. These results suggest that bFGF-heparin and/or heparan sulfate complexes may be more effective than bFGF alone in stimulating cells located away from the bFGF source because the bFGF-glycosaminoglycan complex partitions into the soluble phase rather than binding to insoluble glycosaminoglycans in the extracellular matrix. Thus, the complex of bFGF and glycosaminoglycan may represent one of the active forms of bFGF in vivo.
测量了在存在和不存在糖胺聚糖肝素和硫酸乙酰肝素的情况下碱性成纤维细胞生长因子(bFGF)的扩散半径。碘化的125I-bFGF在肝素存在时比不存在时在琼脂糖、纤维蛋白以及牛主动脉内皮(BAE)细胞单层上扩散得更远。硫酸乙酰肝素对125I-bFGF扩散的影响方式与肝素相似,但程度较弱。当应用于BAE细胞单层中心时,bFGF加肝素刺激形态变化的半径比单独使用bFGF大10倍。这些结果表明,bFGF-肝素和/或硫酸乙酰肝素复合物在刺激远离bFGF来源的细胞方面可能比单独的bFGF更有效,因为bFGF-糖胺聚糖复合物进入可溶性相,而不是与细胞外基质中的不溶性糖胺聚糖结合。因此,bFGF和糖胺聚糖的复合物可能代表bFGF在体内的一种活性形式。