Odontogenic differentiation of human dental pulp stem cells induced by preameloblast-derived factors

Biomaterials. 2011 Dec;32(36):9696-706. doi: 10.1016/j.biomaterials.2011.09.007. Epub 2011 Sep 16.

Abstract

The differentiation of odontoblasts is initiated by the organization of differentiating ameloblasts during tooth formation. However, the exact roles of ameloblast-derived factors in odontoblast differentiation have not yet been characterized. We investigated the effects of preameloblast-conditioned medium (PA-CM) on the odontogenic differentiation of human dental pulp stem cells (hDPSCs) in vitro and in vivo. Furthermore, we analyzed the PA-CM by liquid chromatography-mass spectrometry to identify novel factors that facilitate odontoblast differentiation. In the co-culture of MDPC-23 cells or hDPSCs with mouse apical bud cells (ABCs), ABCs promoted differentiation of odontoblastic MDPC-23 cells and facilitated odontoblast differentiation of hDPSCs. PA-CM, CM from ABCs after 3 days culture, was most effective in increasing the dentin sialophosphoprotein promoter activity of odontoblastic MDPC-23 cells. When PA-CM-treated hDPSCs were transplanted into immunocompromised mice, they generated pulp-like structures lined with human odontoblast-like cells showing typical odontoblast processes. However, during recombinant human bone morphogenenetic protein 2-treated hDPSCs transplantation, some of the cells were entrapped in mineralized matrix possessing osteocyte characteristics. After proteomic analyses, we identified 113 types of proteins in PA-CM, of which we characterized 23. The results show that preameloblast-derived factors induce the odontogenic differentiation of hDPSCs and promote dentin formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Ameloblasts / cytology*
  • Ameloblasts / drug effects
  • Ameloblasts / metabolism
  • Animals
  • Calcification, Physiologic / drug effects
  • Calcification, Physiologic / genetics
  • Cell Differentiation / drug effects*
  • Cell Differentiation / genetics
  • Culture Media, Conditioned / pharmacology*
  • Dental Pulp / cytology*
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism
  • Gene Expression Regulation / drug effects
  • HEK293 Cells
  • Humans
  • Integrin-Binding Sialoprotein / genetics
  • Integrin-Binding Sialoprotein / metabolism
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Odontoblasts / cytology
  • Odontoblasts / drug effects
  • Odontoblasts / ultrastructure
  • Odontogenesis / drug effects*
  • Odontogenesis / genetics
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Promoter Regions, Genetic / genetics
  • Proteomics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Sialoglycoproteins / genetics
  • Sialoglycoproteins / metabolism
  • Stem Cells / cytology*
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Young Adult

Substances

  • Culture Media, Conditioned
  • Extracellular Matrix Proteins
  • Integrin-Binding Sialoprotein
  • Membrane Proteins
  • Phosphoproteins
  • RNA, Messenger
  • Sialoglycoproteins
  • dentin sialophosphoprotein