Activation of αSMA expressing perivascular cells during reactionary dentinogenesis

Int Endod J. 2019 Jan;52(1):68-76. doi: 10.1111/iej.12983. Epub 2018 Jul 26.

Abstract

Aim: To examine the contribution of perivascular cells expressing αSMA to reactionary dentinogenesis.

Methodology: An inducible, Cre-loxP in vivo fate-mapping approach was used to examine the contribution of the descendants of cells expressing the αSMA-CreERT2 transgene to reactionary dentinogenesis in mice molars. Reactionary dentinogenesis was induced by experimental mild injury to dentine without pulp exposure. The Student's t test was used to determine statistical significance at *P ≤ 0.05.

Results: The lineage tracing experiments revealed that mild injury to dentine first led to activation of αSMA-tdTomato+ cells in the entire pulp chamber. The percentage of areas occupied by αSMA-tdTomato+ in injured (7.5 ± 0.7%) teeth were significantly higher than in teeth without injury (2 ± 0.5%). After their activation, αSMA-tdTomato+ cells migrated towards the site of injury, gave rise to pulp cells and a few odontoblasts that became integrated into the existing odontoblast layer expressing Col2.3-GFP and Dspp.

Conclusion: Mild insult to dentine activated perivascular αSMA-tdTomato+ cells giving rise to pulp cells as well as a few odontoblasts that were integrated into the pre-existing odontoblast layer.

Keywords: odontoblasts; perivascular cells; pulp biology; reactionary dentine; αSMA.

MeSH terms

  • Actins / metabolism*
  • Animals
  • Bone Remodeling
  • Cell Movement
  • Dental Pulp / metabolism
  • Dentin / growth & development
  • Dentin / injuries
  • Dentin / pathology
  • Dentinogenesis / physiology*
  • Extracellular Matrix Proteins / metabolism
  • Immunohistochemistry
  • Mice
  • Mice, Transgenic
  • Models, Animal
  • Molar
  • Odontoblasts
  • Phosphoproteins / metabolism
  • Sialoglycoproteins / metabolism

Substances

  • Actins
  • Extracellular Matrix Proteins
  • Phosphoproteins
  • Sialoglycoproteins
  • alpha-smooth muscle actin, mouse
  • dentin sialophosphoprotein