Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia, INSERM UMR 1163, Université de Paris, Imagine Institute, Paris, France.
MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
J Bone Miner Res. 2020 Sep;35(9):1782-1797. doi: 10.1002/jbmr.4042. Epub 2020 May 26.
Gain or loss-of-function mutations in fibroblast growth factor receptor 3 (FGFR3) result in cranial vault defects highlighting the protein's role in membranous ossification. Zebrafish express high levels of fgfr3 during skull development; in order to study FGFR3's role in cranial vault development, we generated the first fgfr3 loss-of-function zebrafish (fgfr3 ). The mutant fish exhibited major changes in the craniofacial skeleton, with a lack of sutures, abnormal frontal and parietal bones, and the presence of ectopic bones. Integrated analyses (in vivo imaging and single-cell RNA sequencing of the osteoblast lineage) of zebrafish fgfr3 revealed a delay in osteoblast expansion and differentiation, together with changes in the extracellular matrix. These findings demonstrate that fgfr3 is a positive regulator of osteogenesis. We conclude that changes in the extracellular matrix within growing bone might impair cell-cell communication, mineralization, and new osteoblast recruitment. © 2020 American Society for Bone and Mineral Research.
成纤维细胞生长因子受体 3(FGFR3)的获得或功能丧失性突变导致颅穹窿缺陷,突出了该蛋白在膜性成骨中的作用。斑马鱼在颅骨发育过程中表达高水平的 fgfr3;为了研究 FGFR3 在颅穹窿发育中的作用,我们生成了第一个 fgfr3 功能丧失性斑马鱼( fgfr3 )。突变鱼的颅面骨骼发生了重大变化,没有骨缝,额骨和顶骨异常,并且存在异位骨。对斑马鱼 fgfr3 的综合分析(成骨细胞谱系的体内成像和单细胞 RNA 测序)表明成骨细胞的扩增和分化延迟,同时细胞外基质发生变化。这些发现表明 fgfr3 是成骨作用的正向调节剂。我们得出结论,生长中的骨骼内细胞外基质的变化可能会损害细胞间通讯、矿化和新成骨细胞的募集。© 2020 美国骨矿研究学会。