| Literature DB >> 31136721 |
C Shi1,2, Y Yuan1, Y Guo1,3, J Jing1,4, T V Ho1, X Han1, J Li1,5, J Feng1, Y Chai1.
Abstract
Bone morphogenetic protein (BMP) signaling performs multiple essential functions during craniofacial development. In this study, we used the adult mouse incisor as a model to uncover how BMP signaling maintains tissue homeostasis and regulates mesenchymal stem cell (MSC) fate by mediating WNT and FGF signaling. We observed a severe defect in the proximal region of the adult mouse incisor after loss of BMP signaling in the Gli1+ cell lineage, indicating that BMP signaling is required for cell proliferation and odontoblast differentiation. Our study demonstrates that BMP signaling serves as a key regulator that antagonizes WNT and FGF signaling to regulate MSC lineage commitment. In addition, BMP signaling in the Gli1+ cell lineage is also required for the maintenance of quiescent MSCs, suggesting that BMP signaling not only is important for odontoblast differentiation but also plays a crucial role in providing feedback to the MSC population. This study highlights multiple important roles of BMP signaling in regulating tissue homeostasis.Entities:
Keywords: cell proliferation; differentiation; growth factor signaling; odontoblast; stem cells; tooth
Year: 2019 PMID: 31136721 PMCID: PMC6616121 DOI: 10.1177/0022034519850812
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116