Osteopromotive carbon dots promote bone regeneration through the PERK-eIF2α-ATF4 pathway

Biomater Sci. 2020 May 19;8(10):2840-2852. doi: 10.1039/d0bm00424c.

Abstract

Bone defects are still an unsolved clinical issue that must be overcome. Carbon dots have shown very promising effects in biological therapy. In the current study, we explored their effects on osteogenesis. Furthermore, we revealed the mechanisms in order to develop novel therapeutic approaches to manage the bone defect. For this study, ascorbic acid carbon dots (CDs) were created by a one-step microwave-assisted method. Results showed that the CDs effectively enhanced matrix mineralization, promoted osteogenic differentiation in vitro, and promoted new bone regeneration in the skull defect model in vivo. Furthermore, our data demonstrated that the ER stress and PERK-eIF2α-ATF4 pathway were activated by the CD-induced increase in intracellular calcium. Taken together, our findings suggest that the PERK pathway plays a critical role in CD-induced osteogenic differentiation, and the CDs created herein have the potential to be used to repair bone defects in clinical practice.

MeSH terms

  • Activating Transcription Factor 4 / metabolism*
  • Animals
  • Ascorbic Acid / pharmacology*
  • Bone Regeneration / drug effects*
  • Carbon / pharmacology*
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Endoplasmic Reticulum Stress / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Microwaves
  • Osteoblasts / drug effects*
  • Osteogenesis / drug effects
  • Particle Size
  • Protein Serine-Threonine Kinases / metabolism*
  • Quantum Dots / chemistry*
  • Surface Properties
  • eIF-2 Kinase / metabolism*

Substances

  • Atf4 protein, mouse
  • Activating Transcription Factor 4
  • Carbon
  • PERK kinase
  • Protein Serine-Threonine Kinases
  • eIF-2 Kinase
  • eIF2alpha kinase, mouse
  • Ascorbic Acid