Filla M S, Dam P, Rapraeger A C
Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison 53706, USA.
J Cell Physiol. 1998 Mar;174(3):310-21. doi: 10.1002/(SICI)1097-4652(199803)174:3<310::AID-JCP5>3.0.CO;2-R.
Binding of fibroblast growth factors (FGFs) to receptor tyrosine kinases (FGFRs) and signaling is facilitated by binding of FGF to heparan sulfate proteoglycans (HSPGs). There are multiple families of HSPGs, including extracellular and cell surface forms. An important and potentially controversial question is whether cell surface forms of HSPGs act as positive or negative regulators of FGF signaling. This study examines the ability of the cell surface HSPG syndecan-1 to regulate FGF binding and signaling. HSPG-deficient Raji lymphoma cells, expressing a transfected syndecan-1 cDNA (Raji S1 cells), were used as HSPG "donor" cells. BaF3 cells, expressing an FGFR1 cDNA (FR1C-11 cells), were used as FGFR "reporter" cells. Using Raji S1 cells preincubated with FGF, it was found that they formed heterotypic aggregates with FR1C-11 cells in the presence of FGF-2, but not FGF-1. In addition, the FR1C-11 cells demonstrated FGF-2, but not FGF-1, dependent survival when cultured on fixed Raji S1 cells. Thus, Raji syndecan-1 1) differentially regulates the binding and signaling of FGFs 1 and 2 and 2) acts as a positive regulator of FGF-2 signaling.
成纤维细胞生长因子(FGFs)与受体酪氨酸激酶(FGFRs)的结合及信号传导是通过FGF与硫酸乙酰肝素蛋白聚糖(HSPGs)的结合来促进的。HSPGs有多个家族,包括细胞外和细胞表面形式。一个重要且可能有争议的问题是,细胞表面形式的HSPGs是作为FGF信号传导的正调节因子还是负调节因子。本研究检测了细胞表面HSPG syndecan-1调节FGF结合和信号传导的能力。缺乏HSPG的Raji淋巴瘤细胞,表达转染的syndecan-1 cDNA(Raji S1细胞),用作HSPG“供体”细胞。表达FGFR1 cDNA的BaF3细胞(FR1C-11细胞)用作FGFR“报告”细胞。使用预先与FGF孵育的Raji S1细胞,发现在FGF-2存在下,它们与FR1C-11细胞形成异型聚集体,但在FGF-1存在下则不然。此外,当在固定的Raji S1细胞上培养时,FR1C-11细胞表现出FGF-2依赖性存活,但不是FGF-1依赖性存活。因此,Raji syndecan-1 1)差异调节FGF-1和FGF-2的结合及信号传导,2)作为FGF-2信号传导的正调节因子。