Abstract

BackgroundOdontoblast is a unique progenitor that plays a role in dentin formation. So far, the dentinogenic differentiation of dental pulp stem cells and the role of surface molecules of odontoblasts in dentinogenesis are not well known yet. In this study, we obtained odontoblast-like cells from human dental pulp cells and screened odontoblast-specific cell surface antigens by decoy immunization.MethodsThrough decoy immunization with intact odontoblast-like cells derived from human dental pulp cells, we constructed 12 monoclonal antibodies (mAbs) of IgG type, and their binding affinities for cell surface of odontoblast-like cells were analyzed by flow cytometry. Immunoprecipitation, mass spectrometry, and immunohistochemistry were performed to demonstrate odontoblast-specific antigens. Odontoblasts were sorted by these mAbs using magnetic-activated cell sorting system, and their mineralization efficiency was increased after sorting.ResultsWe constructed 12 mAbs of IgG type, which had a strong binding affinity for cell surface antigens of odontoblast-like cells. In human adult tooth, these mAbs accumulated in the odontoblastic layer between dentin and pulp and in the perivascular region adjacent to the blood vessels in the pulp core. Cell surface expression of the antigenic molecules was increased during odontogenic cytodifferentiation and decreased gradually as dentinogenic maturation progressed. Proteomic analysis showed that two representative antigenic molecules, OD40 and OD46, had the potential to be components for cell adhesion and extracellular matrix structures.ConclusionThese results suggest that mAbs will be useful for detecting and separating odontoblasts from the primary pulp cells and other lineage cells and will provide information on the structures of extracellular matrix and microenvironment that appears during the dentinogenic differentiation.

Highlights

  • Odontoblast is a unique progenitor that plays a role in dentin formation

  • Dentinogenic differentiation of human adult dental pulp cells by co-treatment of BMP2 and BMP4 To identify the optimal conditions for dentinogenic differentiation, human adult dental pulp cells were treated with various cytokines

  • B Comparison of expression patterns of odontogenic and osteogenic markers in between odontoblast-like cells (a) and osteoblasts (b) by co-treatment with BMP2 and BMP4. hDPC, human dental pulp cells no-treated with Bone morphogenic proteins (BMP); hDPC +BMPs, human dental pulp cells co-treated with BMPs; pre-Human fetal osteoblast (hFOB), human fetal osteoblasts grown at 34 °C; hFOB, human fetal osteoblasts grown at 39 °C for induction of osteo-maturation

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Summary

Introduction

Odontoblast is a unique progenitor that plays a role in dentin formation. So far, the dentinogenic differentiation of dental pulp stem cells and the role of surface molecules of odontoblasts in dentinogenesis are not well known yet. We obtained odontoblast-like cells from human dental pulp cells and screened odontoblast-specific cell surface antigens by decoy immunization. Previous studies with knockout mice revealed that the arrest of tooth development caused by the deletion of Msx and Pax proteins is rescued by BMP4 overexpression [14, 15], and BMP4 signaling converges on Wnt activation during odontogenesis [16]. Both collagen and non-collagenous proteins are produced during odontogenic differentiation. Through direct immunization with intact odontoblasts, we identified several candidate antibodies recognizing odontoblast-specific cell surface antigens

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