Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2006
Substance P stimulates release of RANKL via COX-2 expression in human dental pulp cells.
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Обработка статьи · этапы, ошибки и управление
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История · было → стало
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Kojima T, Yamaguchi M, Kasai K
Аннотация
OBJECTIVE: Our previous study found that substance P (SP), a sensory neuropeptide, was expressed in the dental pulp of rats during experimental tooth movement. We examined the effects of SP on the production of prostaglandin (PG) E2 and the receptor activator of nuclear factor- B ligand (RANKL) by human dental pulp fi broblast-like (HDPF) cells.
MATERIALS AND METHODS: SP was added to cultured HDPF cells at concentrations ranging from of 10(-4) to 10(-12) mol/L. PGE2 and soluble RANKL (sRANKL) levels were determined using enzyme-linked immunosorbent assay kits. Gene expression was confi rmed by RT-PCR analysis. Pit formation assays using dentin slices were carried out to examine the effect of SP on osteoclastogenesis.
RESULTS: The levels of PGE2 and sRANKL increased in the presence of SP, though the increases were greater in the experimental groups in both a time- and concentration-dependent manner, and the increase of RANKL was partially mediated by PGE2. The gene expression of cyclooxygenase (COX)-2 and RANKL was up-regulated, and conditioned medium samples obtained from HDPF cells treated with SP induced bone resorption.
CONCLUSIONS: SP stimulated the production of PGE2 and RANKL, and promoted bone resorption. Therefore, SP may be involved in pulpal inflammation and root resorption during orthodontic tooth movement.
MATERIALS AND METHODS: SP was added to cultured HDPF cells at concentrations ranging from of 10(-4) to 10(-12) mol/L. PGE2 and soluble RANKL (sRANKL) levels were determined using enzyme-linked immunosorbent assay kits. Gene expression was confi rmed by RT-PCR analysis. Pit formation assays using dentin slices were carried out to examine the effect of SP on osteoclastogenesis.
RESULTS: The levels of PGE2 and sRANKL increased in the presence of SP, though the increases were greater in the experimental groups in both a time- and concentration-dependent manner, and the increase of RANKL was partially mediated by PGE2. The gene expression of cyclooxygenase (COX)-2 and RANKL was up-regulated, and conditioned medium samples obtained from HDPF cells treated with SP induced bone resorption.
CONCLUSIONS: SP stimulated the production of PGE2 and RANKL, and promoted bone resorption. Therefore, SP may be involved in pulpal inflammation and root resorption during orthodontic tooth movement.
Предметные рубрики MeSH
AdolescentAdultCarrier ProteinsCell LineCells, CulturedCulture Media, ConditionedCyclooxygenase 2Cyclooxygenase InhibitorsDental PulpDinoprostoneDose-Response Relationship, DrugFemaleHumansMaleMembrane GlycoproteinsMembrane ProteinsNitrobenzenesRANK LigandReceptor Activator of Nuclear Factor-kappa BSubstance PSulfonamides