Chapman Jessica R, Katsara Olga, Ruoff Rachel, Morgenstern David, Nayak Shruti, Basilico Claudio, Ueberheide Beatrix, Kolupaeva Victoria
From the ‡Proteomics Laboratory.
Departments of §Microbiology.
Mol Cell Proteomics. 2017 Jun;16(6):1126-1137. doi: 10.1074/mcp.M116.064980. Epub 2017 Mar 15.
Fibroblast growth factor (FGF) signaling is vital for many biological processes, beginning with development. The importance of FGF signaling for skeleton formation was first discovered by the analysis of genetic FGFR mutations which cause several bone morphogenetic disorders, including achondroplasia, the most common form of human dwarfism. The formation of the long bones is mediated through proliferation and differentiation of highly specialized cells - chondrocytes.Chondrocytes respond to FGF with growth inhibition, a unique response which differs from the proliferative response of the majority of cell types; however, its molecular determinants are still unclear. Quantitative phosphoproteomic analysis was utilized to catalogue the proteins whose phosphorylation status is changed upon FGF1 treatment. The generated dataset consists of 756 proteins. We could localize the divergence between proliferative (canonical) and inhibitory (chondrocyte specific) FGF transduction pathways immediately upstream of AKT kinase. Gene Ontology (GO) analysis of the FGF1 regulated peptides revealed that many of the identified phosphorylated proteins are assigned to negative regulation clusters, in accordance with the observed inhibitory growth response. This is the first time a comprehensive subset of proteins involved in FGF inhibitory response is defined. We were able to identify a number of targets and specifically discover glycogen synthase kinase3β (GSK3β) as a novel key mediator of FGF inhibitory response in chondrocytes.
成纤维细胞生长因子(FGF)信号传导对许多生物过程至关重要,从发育过程就开始发挥作用。FGF信号传导对骨骼形成的重要性最初是通过对导致多种骨形态发生障碍的遗传性FGFR突变进行分析发现的,这些障碍包括软骨发育不全,这是人类侏儒症最常见的形式。长骨的形成是通过高度特化的细胞——软骨细胞的增殖和分化介导的。软骨细胞对FGF的反应是生长抑制,这是一种独特的反应,不同于大多数细胞类型的增殖反应;然而,其分子决定因素仍不清楚。利用定量磷酸化蛋白质组学分析对FGF1处理后磷酸化状态发生变化的蛋白质进行分类。生成的数据集包含756种蛋白质。我们能够在AKT激酶的紧邻上游定位增殖性(经典)和抑制性(软骨细胞特异性)FGF转导途径之间的差异。对FGF1调节肽的基因本体(GO)分析表明,根据观察到的抑制性生长反应,许多已鉴定的磷酸化蛋白质被归类为负调控簇。这是首次定义参与FGF抑制反应的蛋白质的全面子集。我们能够识别多个靶点,并特别发现糖原合酶激酶3β(GSK3β)是软骨细胞中FGF抑制反应的一种新型关键介质。