| Literature DB >> 29649366 |
I Vidovic-Zdrilic1, K H Vining2, A Vijaykumar1, I Kalajzic3, D J Mooney2, M Mina1.
Abstract
The goal of this study was to examine the effects of early and limited exposure of perivascular cells expressing α (αSMA) to fibroblast growth factor 2 (FGF2) in vivo. We performed in vivo fate mapping by inducible Cre-loxP and experimental pulp injury in molars to induce reparative dentinogenesis. Our results demonstrate that early delivery of exogenous FGF2 to exposed pulp led to proliferative expansion of αSMA-tdTomato+ cells and their accelerated differentiation into odontoblasts. In vivo lineage-tracing experiments showed that the calcified bridge/reparative dentin in FGF2-treated pulps were lined with an increased number of Dspp+ odontoblasts and devoid of BSP+ osteoblasts. The increased number of odontoblasts derived from αSMA-tdTomato+ cells and the formation of reparative dentin devoid of osteoblasts provide in vivo evidence for the stimulatory effects of FGF signaling on odontoblast differentiation from early progenitors in dental pulp.Entities:
Keywords: dentin matrix protein 1 (DMP1); dentin sialophosphoprotein (DSPP); perivascular cells; pulp biology; reparative dentinogenesis; stem cells
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Year: 2018 PMID: 29649366 PMCID: PMC6169028 DOI: 10.1177/0022034518769827
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116