Thompson L M, Raffioni S, Wasmuth J J, Bradshaw R A
Department of Biological Chemistry, College of Medicine, University of California, Irvine 92697, USA.
Mol Cell Biol. 1997 Jul;17(7):4169-77. doi: 10.1128/MCB.17.7.4169.
Mutations in the gene for human fibroblast growth factor receptor 3 (hFGFR3) cause a variety of skeletal dysplasias, including the most common genetic form of dwarfism, achondroplasia (ACH). Evidence indicates that these phenotypes are not due to simple haploinsufficiency of FGFR3 but are more likely related to a role in negatively regulating skeletal growth. The effects of one of these mutations on FGFR3 signaling were examined by constructing chimeric receptors composed of the extracellular domain of human platelet-derived growth factor receptor beta (hPDGFR beta) and the transmembrane and intracellular domains of hFGFR3 or of an ACH (G375C) mutant. Following stable transfection in PC12 cells, which lack platelet-derived growth factor (PDGF) receptors, all clonal cell lines, with either type of chimera, showed strong neurite outgrowth in the presence of PDGF but not in its absence. Antiphosphotyrosine immunoblots showed ligand-dependent autophosphorylation, and both receptor types stimulated strong phosphorylation of mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase, an event associated with the differentiative response of these cells. In addition, ligand-dependent phosphorylation of phospholipase Cgamma and Shc was also observed. All of these responses were comparable to those observed from ligand activation, such as by nerve growth factor, of the native PC12 cells used to prepare the stable transfectants. The cells with the chimera bearing the ACH mutation were more rapidly responsive to ligand with less sustained MAPK activation, indicative of a preactivated or primed condition and consistent with the view that these mutations weaken ligand control of FGFR3 function. However, the full effect of the mutation likely depends in part on structural features of the extracellular domain. Although FGFR3 has been suggested to act as a negative regulator of long-bone growth in chrondrocytes, it produces differentiative signals similar to those of FGFR1, to which only positive effects have been ascribed, in PC12 cells. Therefore, its regulatory effects on bone growth likely result from cellular contexts and not the induction of a unique FGFR3 signaling pathway.
人类成纤维细胞生长因子受体3(hFGFR3)基因的突变会导致多种骨骼发育异常,包括最常见的侏儒症遗传形式——软骨发育不全(ACH)。有证据表明,这些表型并非由于FGFR3的单倍体不足,而更可能与负向调节骨骼生长的作用有关。通过构建由人血小板衍生生长因子受体β(hPDGFRβ)的胞外结构域与hFGFR3或ACH(G375C)突变体的跨膜和胞内结构域组成的嵌合受体,研究了其中一种突变对FGFR3信号传导的影响。在缺乏血小板衍生生长因子(PDGF)受体的PC12细胞中进行稳定转染后,所有带有任一类型嵌合体的克隆细胞系在有PDGF存在时均表现出强烈的神经突生长,而在无PDGF时则无此现象。抗磷酸酪氨酸免疫印迹显示配体依赖性自磷酸化,并且两种受体类型均刺激丝裂原活化蛋白激酶(MAPK)/细胞外信号调节激酶的强烈磷酸化,这一事件与这些细胞的分化反应相关。此外,还观察到磷脂酶Cγ和Shc的配体依赖性磷酸化。所有这些反应与用于制备稳定转染体的天然PC12细胞经配体激活(如神经生长因子激活)所观察到的反应相当。带有ACH突变的嵌合体的细胞对配体的反应更快,MAPK激活的持续时间更短,这表明处于预激活或启动状态,与这些突变削弱FGFR3功能的配体控制这一观点一致。然而,该突变的全部效应可能部分取决于胞外结构域的结构特征。尽管FGFR3被认为在软骨细胞中作为长骨生长的负调节因子起作用,但在PC12细胞中它产生的分化信号与FGFR1相似,而FGFR1仅被归因于具有正向作用。因此,其对骨骼生长的调节作用可能源于细胞环境,而非诱导独特的FGFR3信号通路。