Expression of Mineralization Markers in Dental Pulp Cells
Xi Wei, MS, MDS,* Junqi Ling, PhD,* Liping Wu, MS,* Lu Liu, MD,* and Yin Xiao, PhD†
Abstract
There is an increasing interest in the utility of dental pulp
stem cells (DPSCs) for dentin regeneration. The mechanisms
involved in DPSC differentiation remain poorly understood.
The purpose of the study was to investigate the
mineralization capacity of human dental pulp cells (DPCs)
and identify potential markers for odontoblast differentiation.
The isolated DPCs expressed mesenchymal stemcell
markers as shown by flow cytometry and could differentiate
in vitro into odontogenic, adipogenic, and
chondrogenic lineages. Alkaline phosphatase activity of
DPCs elevated over time, with significant upregulation on
day 21 in odontogenic induction. Quantitative RT-PCR
revealed that osteocalcin, dentin sialophosphoprotein
(DSPP), and matrix extracellular phosphoglycoprotein
(MEPE) expression also increased time dependently in the
induction cultures. In conclusion, we isolated DPCs with
stem cell characteristics. MEPE and DSPP showed a similar
regulatory pattern of DPCs mineralization. MEPE along
with DSPP may be potential odontogenetic differentiation
markers. (J Endod 2007;33:703–708)
牙髓细胞矿化标志物的表达
牙髓干细胞重建牙本质越来越受到关注。人们对牙髓干细胞的分化机制了解不多,本研究旨在检测人牙髓干细胞矿化能力和明确成牙分化的可能标志物。分离的人牙髓下随时间增加,在21天最高。干细胞表达间充质干细胞的表面标志,可以向成牙,成脂,成软骨分化。人牙髓细胞碱磷酶活性在成牙诱导实时PCR显示在诱导环境下,OCN,DSPP,MEPE随时间增加。因此,分离出的牙髓细胞有干细胞性质,MEPE和DSPP可能是成牙分化的标志。