Different concentrations of fetal bovine serum affect cytokine modulation in Lipopolysaccharide- activated apical papilla cells in vitro

Autor(es)

Santos, Leticia Martins ; Cardoso, Patricia e Silva ; Diniz, Elisa Abreu ; Rahhal, Juliana Garuba ; Sipert, Carla Renata

• Tipo de documento: Artigo Científico
• Fonte: Journal of Applied Oral Science; v. 31, p. 9-pg., 2023-01-01.

Resumo

Fetal bovine serum (FBS) is the most used supplement in culture media; however, it may interfere with in vitro assays via effects on cell proliferation and cytokine production. The ideal FBS concentration for assays using apical papilla cells (APCs) remains unknown. Therefore, this study aimed to evaluate the effects of FBS on APC activation, cell viability/proliferation, and cytokine production. Methodology: Human APCs were cultured, plated, and maintained in media containing increasing concentrations of FBS for 24 h, 48 h, 72 h, 7 days, and 14 days in the presence of Lipopolysaccharide (LPS -1 & mu;g/mL). At each time point, the cells were subjected to the MTT assay. The cytokines transforming growth factor (TGF)-& beta;1, osteoprotegerin (OPG), and interleukin (IL)-6, along with the chemokine CCL2, were quantified using the enzyme -linked immunosorbent assay at the 24-h time-point. Statistical analysis was performed using two-way analysis of variance (ANOVA) followed by Tukey's post-hoc test (p<0.05). Results: In general, APCs exhibited increasing metabolic activity in an FBS concentration-dependent fashion, regardless of the presence of LPS. In contrast, FBS interfered with the production of all the cytokines evaluated in this study, affecting the response induced by the presence of LPS. Conclusion: FBS increased APC metabolism in a concentration-dependent manner and differentially affected the production of TGF-& beta;1, OPG, IL-6, and CCL2 by APCs in vitro. (AU)

• Processo FAPESP: 20/12726-0 - Papel da osteoprotegerina na modulação in vitro de monócitos por células de papila apical
• Beneficiário: Carla Renata Sipert
• Modalidade de apoio: Auxílio à Pesquisa - Regular