Jagged1 promotes mineralization in human bone-derived cells

Arch Oral Biol. 2019 Mar:99:134-140. doi: 10.1016/j.archoralbio.2019.01.013. Epub 2019 Jan 18.

Abstract

Objectives: The present study aimed to investigate the expression of Notch signaling components during osteogenic differentiation in vitro and bone healing in vivo. In addition, the influence of Notch signaling on osteogenic differentiation of human bone-derived cells was examined.

Methods: Gene expression profiling of osteogenic differentiation of human bone marrow-derived mesenchymal stromal cells in vitro (GSE80614) and bone healing period of murine tibial fracture in vivo (GSE99388) was downloaded from Gene Expression Omnibus database. The expression of Notch signaling components was obtained from bioinformatic tools. Human bone-derived cells were isolated from alveolar and iliac bone. Cells were seeded on Jagged1 immobilized surface. Osteogenic marker gene expression and mineralization were examined using real-time polymerase chain reaction and alizarin red s staining, respectively.

Results: From bioinformatic analysis of gene expression profiling, various Notch signaling components were differentially expressed during osteogenic differentiation of human bone marrow-derived mesenchymal stromal cells in vitro and bone healing period of murine tibial fracture in vivo. The common genes differentially regulated of these two datasets were Hes1, Aph1a, Nsctn, Furin, Adam17, Hey1, Pcsk5, Nedd4, Jag1, Heyl, Notch3, Dlk1, and Hey2. For an in vitro analysis, the mineral deposition markedly increased after seeding human bone-derived cells on Jagged1 immobilized surface, correspondingly with the increase of ALP mRNA expression. Jagged1 treatment downregulated TWIST2 mRNA expression in both human alveolar and iliac bone-derived cells.

Conclusion: Notch signaling is regulated during osteogenic differentiation and bone healing. In addition, the activation of Notch signaling promotes osteogenic differentiation in human alveolar and iliac bone-derived cells. Therefore, Notch signaling manipulation could be a useful approach for enhancing bone regeneration.

Keywords: Bone; Mineralization; Notch signaling; Osteogenic differentiation.

MeSH terms

  • ADAM17 Protein / genetics
  • Alveolar Epithelial Cells / drug effects
  • Alveolar Epithelial Cells / metabolism
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Bone Regeneration / drug effects
  • Bone Regeneration / physiology
  • Calcification, Physiologic / drug effects
  • Calcification, Physiologic / physiology*
  • Calcium-Binding Proteins
  • Cell Cycle Proteins / genetics
  • Cell Differentiation
  • Endopeptidases / genetics
  • Furin / genetics
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Humans
  • Ilium / drug effects
  • Ilium / metabolism
  • Intercellular Signaling Peptides and Proteins / genetics
  • Jagged-1 Protein / genetics
  • Jagged-1 Protein / metabolism*
  • Jagged-1 Protein / pharmacology
  • Membrane Proteins
  • Mesenchymal Stem Cells
  • Mice
  • Nedd4 Ubiquitin Protein Ligases / genetics
  • Osteocytes / drug effects
  • Osteocytes / metabolism*
  • Osteogenesis / genetics
  • Osteogenesis / physiology*
  • Proprotein Convertase 5
  • RNA, Messenger
  • Receptor, Notch3 / genetics
  • Receptors, Notch / genetics
  • Receptors, Notch / metabolism*
  • Repressor Proteins / genetics
  • Signal Transduction*
  • Tibial Fractures / genetics
  • Tibial Fractures / metabolism
  • Transcription Factor HES-1 / genetics

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Calcium-Binding Proteins
  • Cell Cycle Proteins
  • Dlk1 protein, mouse
  • Hes1 protein, mouse
  • Hey1 protein, mouse
  • Hey2 protein, mouse
  • Heyl protein, mouse
  • Intercellular Signaling Peptides and Proteins
  • JAG1 protein, human
  • Jag1 protein, mouse
  • Jagged-1 Protein
  • Membrane Proteins
  • Notch3 protein, mouse
  • RNA, Messenger
  • Receptor, Notch3
  • Receptors, Notch
  • Repressor Proteins
  • Transcription Factor HES-1
  • Nedd4 Ubiquitin Protein Ligases
  • Nedd4 protein, mouse
  • Endopeptidases
  • Proprotein Convertase 5
  • propeptide convertase 5, mouse
  • Furin
  • ADAM17 Protein
  • Adam17 protein, mouse
  • Aph1a protein, mouse