Fluoride effects on cell viability and ENaC expression in kidney epithelial cells

• Published in: Toxicology mechanisms and methods Vol. 31; no. 8; pp. 566 - 571
• Main Authors: Santesso, Mariana R., Oliveira, Flávia A., Tokuhara, Cintia K., Oliveira, Gabriela S. N., Levy, Flávia M., Antonio, Lígia S., Buzalaf, Marília A. R., Oliveira, Rodrigo C.
• Format: Journal Article
• Language: English
• Published: Taylor & Francis 13-10-2021
• Subjects: ENaC; Fluoride; kidney epithelial cells; M-1 cells; NaF
• ISSN: 1537-6516; 1537-6524
• DOI: 10.1080/15376516.2021.1938325

Fluoride (F) at micromolar (µM) concentrations induces apoptosis in several cell lines. Moreover, proteomic studies have shown major changes in the profile of proteins involved in signal transduction. These effects may negatively affect ion transport in the kidneys. The activity of epithelial sodium channels (ENaCs) is a limiting factor for sodium and water resorption in the kidneys, which is essential for the maintenance of the electrolyte balance and homeostasis of the body. Here we investigated the effects of F, at different concentrations (10, 40, 100, 200, and 400 μM), on the viability of renal epithelial cells (M-1), and ENaC expression. We showed that sodium fluoride (NaF) reduces cell viability in a concentration-dependent manner (p < 0.05) up to a 96-h time-point when compared to control. Sodium fluoride at moderate concentrations (100 and 200 μM), upregulated the ENaC subunit genes Scnn1a and Scnn1g, but not Scnn1b. Sodium fluoride downregulated all three ENaC subunit genes at a higher concentration of 400 μM (p < 0.05). Immunofluorescence analysis showed that Scnn1a and Scnn1g expression was decreased within 24 h of NaF treatment. After 48 h, NaF (400 μM) increased the expression of Scnn1a but not Scnn1g. However, NaF decreased the expression of Scnn1g at all studied concentrations. We conclude that F, at µM concentrations, modulates the expression of ENaC subunit genes, which is likely to significantly affect molecular signaling in kidney epithelial cells.