Enamel fluorosis is a defect in enamel development that occurs after exposure to excess fluoride. Fluorotic enamel is more porous, and contains more proteins than sound enamel. The mechanisms by which fluoride alters enamel formation remain not well understood. In this competing renewal, we propose studies to begin to explore the indirect effects of fluoride resulting from changes in the forming enamel matrix, secondary to fluoride incorporation in the growth of enamel crystals. We will also continue to explore the direct effects of fluoride on the cells, matrix proteins, and proteinases that form enamel. We hypothesize that both of these effects of fluoride on enamel formation are mechanisms by which fluoride alters enamel formation, and propose the following Specific Aims: 1). To determine the indirect effects of fluoride on enamel formation and biomineralization, including acidification of the enamel space that indirectly affects cell and matrix function. 2). To determine how fluoride interacts with enamel proteins including amelogenins and proteinases resulting in changes of amelogenin processing and crystal growth. 3) To determine how fluoride directly affects ameloblast differentiation, including altered expression of matrix proteins and proteinases, and apoptosis. The changes in pH resulting from fluoride exposure will be measured, and the effect of amelogenin and bicarbonate buffering in the enamel matrix and in the ameloblasts will be determined in amelogenin knockout mice and HCO37C1 (Ae2) exchange knockout mice. The direct interactions of fluoride with amelogenins and matrix proteinases, and the effect on crystal growth will be measured in an in vitro crystal growth system. We will use ameloblast cell culture to identify fluoride related changes in gene expression related to cell proliferation, apoptosis, and measure changes in activity of matrix enzymes that are related to mineralization. These studies are important to understand how fluorosis forms in enamel. By understanding the mechanisms by which fluorosis occurs, we will be able to identify individuals and conditions which may be more sensitive to or affected by fluoride, and will be better able to prevent the formation of enamel fluorosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE013508-09
Application #
7465529
Study Section
Special Emphasis Panel (ZRG1-MOSS-E (02))
Program Officer
Shum, Lillian
Project Start
1999-12-01
Project End
2010-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
9
Fiscal Year
2008
Total Cost
$345,569
Indirect Cost
Name
University of California San Francisco
Department
Anatomy/Cell Biology
Type
Schools of Dentistry
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Varga, G; DenBesten, P; Rácz, R et al. (2018) Importance of bicarbonate transport in pH control during amelogenesis - need for functional studies. Oral Dis 24:879-890
Rácz, Róbert; Földes, Anna; Bori, Erzsébet et al. (2017) No Change in Bicarbonate Transport but Tight-Junction Formation Is Delayed by Fluoride in a Novel Ameloblast Model. Front Physiol 8:940
Le, Michael H; Nakano, Yukiko; Abduweli Uyghurturk, Dawud et al. (2017) Fluoride Alters Klk4 Expression in Maturation Ameloblasts through Androgen and Progesterone Receptor Signaling. Front Physiol 8:925
Bori, E; Guo, J; Rácz, R et al. (2016) Evidence for Bicarbonate Secretion by Ameloblasts in a Novel Cellular Model. J Dent Res 95:588-96
Bronckers, A L J J; Lyaruu, D; Jalali, R et al. (2015) Ameloblast Modulation and Transport of Cl?, Na?, and K? during Amelogenesis. J Dent Res 94:1740-7
Guo, J; Lyaruu, D M; Takano, Y et al. (2015) Amelogenins as potential buffers during secretory-stage amelogenesis. J Dent Res 94:412-20
Bronckers, Antonius L J J; Lyaruu, Don M; Guo, Jing et al. (2015) Composition of mineralizing incisor enamel in cystic fibrosis transmembrane conductance regulator-deficient mice. Eur J Oral Sci 123:9-16
Jalali, R; Zandieh-Doulabi, B; DenBesten, P K et al. (2015) Slc26a3/Dra and Slc26a6 in Murine Ameloblasts. J Dent Res 94:1732-9
Lyaruu, D M; Medina, J F; Sarvide, S et al. (2014) Barrier formation: potential molecular mechanism of enamel fluorosis. J Dent Res 93:96-102
Lyaruu, Donacian M; Schoonderwoerd, Mark; Tio, Dane et al. (2014) Parenteral monofluorophosphate (MFP) is a more potent inducer of enamel fluorotic defects in neonatal hamster molars than sodium fluoride. Odontology 102:147-53

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