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Fgfr3 Is a Positive Regulator of Osteoblast Expansion and Differentiation During Zebrafish Skull Vault Development.

Emilie DambroiseIvan KtorzaAlessandro BrombinGhaith AbdessalemJoanne EdouardMarine LukaImke FiedlerOlivia BinderOlivier PelleE Elizabeth PattonBjörn BusseMickaël MenagerFrederic SohmLaurence Legeai-Mallet
Published in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2020)
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 (fgfr3lof/lof ). 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 fgfr3lof/lof 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.
Keyphrases
  • single cell
  • extracellular matrix
  • rna seq
  • bone regeneration
  • high throughput
  • transcription factor
  • cell therapy
  • stem cells
  • functional connectivity
  • protein protein
  • photodynamic therapy
  • wild type