Guimond S E, Turnbull J E
School of Biosciences, Molecular Cell Biology Research Laboratories, University of Birmingham, Edgbaston, B15 2TT, England, UK.
Curr Biol. 1999 Nov 18;9(22):1343-6. doi: 10.1016/s0960-9822(00)80060-3.
Signalling by fibroblast growth factors (FGFs) through FGF receptors (FGFRs) depends on the cell-surface polysaccharide heparan sulphate (HS) [1] [2]. HS has an ordered domain structure of highly diverse saccharide motifs that present unique displays of sulphate, carboxyl and hydroxyl groups [3]. These motifs interact with many proteins, particularly growth factors. HS binds both to FGFs [4] [5] [6] and FGFRs [7], and probably activates signalling by facilitating ligand-induced receptor dimerisation [8] [9]. Nevertheless, the extent to which specific HS saccharide sequences play a regulatory role has not been established. By screening a library of structurally diverse HS decasaccharides in bioassays of FGF signalling mediated by three different FGFR isoforms, we found that saccharides showed specificity for both ligands and receptors; some saccharides selectively activated FGF signalling through different FGFR isoforms, others acted as negative regulators. We conclude that HS saccharides play critical roles in dictating the specificity of ligand-receptor interactions in FGFR signalling. Controlled alterations in HS structures [10] would provide a mechanism for regulation of cellular responsiveness to growth factors that bind HS.
成纤维细胞生长因子(FGFs)通过成纤维细胞生长因子受体(FGFRs)进行信号传导依赖于细胞表面多糖硫酸乙酰肝素(HS)[1][2]。HS具有高度多样的糖基序的有序结构域结构,这些糖基序呈现出独特的硫酸根、羧基和羟基展示[3]。这些基序与许多蛋白质相互作用,特别是生长因子。HS既与FGFs[4][5][6]结合,也与FGFRs[7]结合,并且可能通过促进配体诱导的受体二聚化来激活信号传导[8][9]。然而,特定的HS糖序列发挥调节作用的程度尚未确定。通过在由三种不同FGFR亚型介导的FGF信号传导的生物测定中筛选结构多样的HS十糖文库,我们发现糖类对配体和受体都具有特异性;一些糖类通过不同的FGFR亚型选择性地激活FGF信号传导,另一些则作为负调节剂。我们得出结论,HS糖类在决定FGFR信号传导中配体 - 受体相互作用的特异性方面起着关键作用。HS结构的可控改变[10]将为调节细胞对结合HS的生长因子的反应性提供一种机制。