Nurcombe V, Ford M D, Wildschut J A, Bartlett P F
Department of Anatomy and Cell Biology, University of Melbourne, Parkville, Australia.
Science. 1993 Apr 2;260(5104):103-6. doi: 10.1126/science.7682010.
Murine neural precursor cells and cell lines derived from them are stimulated by members of the heparin-binding fibroblast growth factor (FGF) family. The activity of FGF is regulated by heparan sulfate proteoglycans (HSPGs), and this interaction is an essential prerequisite for the binding of growth factor to the signal transducing receptors. Messenger RNA for FGF-2 was detectable in the neuroepithelium at embryonic day 9, and the HSPGs produced by these cells at this time preferentially bound FGF-2. However, at embryonic day 11, when messenger RNA for FGF-1 was first detectable, there was a switch in the binding specificity of the HSPG to FGF-1. Thus, a single species of HSPG undergoes a rapid, tightly controlled change in growth factor-binding specificity concomitant with the temporal expression of the FGFs.
小鼠神经前体细胞及其衍生的细胞系受到肝素结合成纤维细胞生长因子(FGF)家族成员的刺激。FGF的活性受硫酸乙酰肝素蛋白聚糖(HSPG)调节,这种相互作用是生长因子与信号转导受体结合的必要前提。在胚胎第9天的神经上皮中可检测到FGF-2的信使核糖核酸,此时这些细胞产生的HSPG优先结合FGF-2。然而,在胚胎第11天,当首次检测到FGF-1的信使核糖核酸时,HSPG对FGF-1的结合特异性发生了转变。因此,单一类型的HSPG在生长因子结合特异性方面经历了快速、严格控制的变化,这与FGF的时序表达相伴。