Journal of Dental Research · 2003 · 60 citations · 20 references
DentistryOral BiologyOral PathologyDental Pulp BiologyOral ImmunologyPulp BiologyDental PulpDentin HistologyOdontoblast BiologyPulp Defense MechanismsPulp ImmunologyPulp InflammationAntigen Presenting CellsAntigen-presenting Cell MaturationDentin-pulp SignalingImmune Cell MigrationPulp Immune CellsPulp Immune FunctionPulp Immune ResponsePulpal Immune Cells
TGF-beta1 released from dentin degraded by bacterial or iatrogenic agents is suspected to influence dental pulp response, including the modulation of cell migration. To determine the consequences of TGF-beta1 action on pulp immune cells, we analyzed, by immunohistochemistry, the effect of transdentinally diffusing TGF-beta1 on their localization in a human tooth slice culture model. TGF-beta1 induced an accumulation of HLA-DR-positive cells in both odontoblast and subodontoblast layers of the stimulated zone. Together with HLA-DR, these cells co-expressed Factor XIIIa and CD68, two features of immature antigen-presenting dendritic cells (DC), as well as the TGF-beta1 specific receptor TbetaRII. In contrast, no effect could be detected on the localization of either mature DC-LAMP-positive DC or of T- and B-lymphocytes. Analysis of these data suggests that TGF-beta1 released from dentin degraded by bacterial or iatrogenic agents could be involved in the immune response of the dental pulp resulting from tooth injury.
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