| Literature DB >> 27834664 |
I Vidovic1, A Banerjee1, R Fatahi2, B G Matthews2, N A Dyment2, I Kalajzic2, M Mina1.
Abstract
The goal of this study was to examine the contribution of perivascular cells to odontoblasts during the development, growth, and repair of dentin using mouse molars as a model. We used an inducible, Cre-loxP in vivo fate-mapping approach to examine the contributions of the descendants of cells expressing the αSMA-CreERT2 transgene to the odontoblast lineage. In vivo lineage-tracing experiments in molars showed the contribution of αSMA-tdTomato+ cells to a small number of newly formed odontoblasts during primary dentinogenesis. Using an experimental pulp exposure model in molars to induce reparative dentinogenesis, we demonstrate the contribution of αSMA-tdTomato+ cells to cells secreting reparative dentin. Our results demonstrate that αSMA-tdTomato+ cells differentiated into Col2.3-GFP+ cells composed of both Dspp+ odontoblasts and Bsp+ osteoblasts. Our findings identify a population of mesenchymal progenitor cells capable of giving rise to a second generation of odontoblasts during reparative dentinogenesis. This population also makes a small contribution to odontoblasts during primary dentinogenesis.Entities:
Keywords: dentin sialophosphoprotein; dentinogenesis; odontoblasts; pulp biology; reparative dentin; stem cells
Mesh:
Substances:
Year: 2016 PMID: 27834664 PMCID: PMC5298392 DOI: 10.1177/0022034516678208
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116