Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis

Sci Rep. 2020 Nov 19;10(1):20216. doi: 10.1038/s41598-020-77161-4.

Abstract

The interaction between immune cells and stem cells is important during tissue repair. Macrophages have been described as being crucial for limb regeneration and in certain circumstances have been shown to affect stem cell differentiation in vivo. Dentine is susceptible to damage as a result of caries, pulp infection and inflammation all of which are major problems in tooth restoration. Characterising the interplay between immune cells and stem cells is crucial to understand how to improve natural repair mechanisms. In this study, we used an in vivo damage model, associated with a macrophage and neutrophil depletion model to investigate the role of immune cells in reparative dentine formation. In addition, we investigated the effect of elevating the Wnt/β-catenin pathway to understand how this might regulate macrophages and impact upon Wnt receiving pulp stem cells during repair. Our results show that macrophages are required for dental pulp stem cell activation and appropriate reparative dentine formation. In addition, pharmacological stimulation of the Wnt/β-catenin pathway via GSK-3β inhibitor small molecules polarises macrophages to an anti-inflammatory state faster than inert calcium silicate-based materials thereby accelerating stem cell activation and repair. Wnt/β-catenin signalling thus has a dual role in promoting reparative dentine formation by activating pulp stem cells and promoting an anti-inflammatory macrophage response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Dental Pulp / drug effects
  • Dental Pulp / metabolism*
  • Dentinogenesis / drug effects
  • Dentinogenesis / physiology*
  • Enzyme Inhibitors / pharmacology
  • Glycogen Synthase Kinase 3 beta / antagonists & inhibitors
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Mice
  • Molar / drug effects
  • Molar / metabolism
  • Wnt Signaling Pathway / drug effects

Substances

  • Enzyme Inhibitors
  • Glycogen Synthase Kinase 3 beta