Vitamin D promotes odontogenic differentiation of human dental pulp cells via ERK activation

Abstract

The active metabolite of vitamin D such as 1α25-dihydroxyvitamin D3 (1α25(OH)2D3) is a well-known key regulatory factor in bone metabolism. However, little is known about the potential of vitamin D as an odontogenic inducer in human dental pulp cells (HDPCs) in vitro. The purpose of this study was to evaluate the effect of vitamin D3 metabolite, 1α25(OH)2D3, on odontoblastic differentiation in HDPCs. HDPCs extracted from maxillary supernumerary incisors and third molars were directly cultured with 1α25(OH)2D3 in the absence of differentiation-inducing factors. Treatment of HDPCs with 1α25(OH)2D3 at a concentration of 10 nM or 100 nM significantly upregulated the expression of dentin sialophosphoprotein (DSPP) and dentin matrix protein1 (DMP1), the odontogenesis-related genes. Also, 1α25(OH)2D3 enhanced the alkaline phosphatase (ALP) activity and mineralization in HDPCs. In addition, 1 α25(OH)2D3 induced activation of extracellular signal regulated kinases (ERKs), whereas the ERK inhibitor U0126 ameliorated the upregulation of DSPP and DMP1 and reduced the mineralization enhanced by 1α25(OH)2D3. These results demonstrated that 1α25(OH)2D3 promoted odontoblastic differentiation of HDPCs via modulating ERK activation.