Effects of Bio-Oss® and Cerasorb® dental M on the expression of bone-remodeling mediators in human monocytes.
Filipe de Assis GonzagaTatiana Teixeira de MirandaLuisa Mourão Dias MagalhãesWalderez Ornelas DutraKenneth John GollobPaulo Eduardo Alencar SouzaMartinho Campolina Rebello HortaPublished in: Journal of biomedical materials research. Part B, Applied biomaterials (2016)
In contribution to diverse techniques of bone reconstruction involving biomaterials in contemporary dentistry, this study aimed to evaluate the effect of the bone-grafting materials Bio-Oss® and Cerasorb® Dental M on the expression of cytokines associated with bone remodeling by human monocytes in vitro. Bio-Oss® and Cerasorb® Dental M were incubated in separate culture media, and their supernatants were added to mononuclear cells of human peripheral blood, some of which had been stimulated with Porphyromonas gingivalis. The frequency of total monocytes and CD14+ monocytes producing cytokines interleukin 6 (IL-6), IL-8, IL-10, IL-12, and tumor necrosis factor alpha (TNF-α) were determined by flow cytometry. One-way analysis of variance with repeated measures, followed by Tukey's post hoc test, revealed that stimulation with P. gingivalis increased the expression of IL-6 and IL-8 and reduced the expression of TNF-α compared to effects demonstrated in the control group (p < 0.05). Adding biomaterial supernatants did not significantly affect the expression of any cytokine evaluated, however, either in the absence or in the presence of bacterial stimulation. Our data suggest that Bio-Oss® and Cerasorb® Dental M neither stimulate cytokine production in human monocytes nor interfere with mechanisms of cell communication mediated by cytokines evaluated during stimulation with P. gingivalis. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 2066-2073, 2017.
Keyphrases
- peripheral blood
- poor prognosis
- endothelial cells
- rheumatoid arthritis
- induced pluripotent stem cells
- bone mineral density
- dendritic cells
- pluripotent stem cells
- oral health
- binding protein
- single cell
- stem cells
- long non coding rna
- induced apoptosis
- immune response
- postmenopausal women
- mesenchymal stem cells
- bone loss
- cell proliferation
- body composition
- endoplasmic reticulum stress
- pi k akt