The process of amelogenesis comprises several well-defined stages culminating in highly mineralized mature enamel. Disturbances (e.g., ingestion of fluoride at higher than optimum doses) at any of those stages result in a defective enamel structure which may be aesthetically undesirable, less resistant to physical wearing, or more susceptible to caries formation. The present proposal attempts to gain information on the following points: 1) Characterization of the physical chemical properties of the medium in which enamel crystallites are formed. Of particular importance is the determination of the calcium, phosphate and pH values of the fluid in the initial (cheese-like) stage of enamel formation. Special microanalytical techniques will be used for that purpose in conjunction with bovine and porcine enamel. The proteins associated with the enamel will be examined electrophoretically. 2) The surface pools of Ca and P of the enamel crystals from the secretory, transitional and maturing stages will be determined by isotopic exchange with 45Ca and 33P to obtain information on the nature (and possible transformations) of the growing mineral. Further characterization of the enamel surface will be done through adsorption experiments using small synthetic peptides as adsorbates and, also, through crystal growth experiments using the deproteinated enamel as seeds in solutions supersaturated with respect to calcium hydroxyapatite. 3) The interaction of amelogenins and enamelins with apatitic surfaces will be investigated using model systems, i.e., determining their adsorption isotherms onto hydroxyapatite. 4) The possible orientation of apatitic crystals by permselective membranes. This kind of experimentation is a first approximation to a postulated mechanism in which the orientation of the enamel crystallites (perpendicular to the Tomes processes) is determined by the electrochemical properties of the membrane and the direction of flow of one limiting ion, i.e., calcium. It is proposed to study the aspects described above first with bovine and porcine enamel and then with rats. With the rat model, the investigation will cover animal under various fluoride regimes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
1R01DE007623-01
Application #
3221277
Study Section
Oral Biology and Medicine Study Section (OBM)
Project Start
1986-03-01
Project End
1989-02-28
Budget Start
1986-03-01
Budget End
1987-02-28
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Forsyth Institute
Department
Type
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02142
Aoba, T (1996) Recent observations on enamel crystal formation during mammalian amelogenesis. Anat Rec 245:208-18
Aoba, T; Taya, Y; Sato, A et al. (1995) Mechanistic understanding of enamel mineralization under fluoride regime. Connect Tissue Res 33:145-9
Aoba, T (1994) Strategies for improving the assessment of dental fluorosis: focus on chemical and biochemical aspects. Adv Dent Res 8:66-74
Goto, Y; Kogure, E; Takagi, T et al. (1993) Molecular conformation of porcine amelogenin in solution: three folding units at the N-terminal, central, and C-terminal regions. J Biochem 113:55-60
Miake, Y; Shimoda, S; Fukae, M et al. (1993) Epitaxial overgrowth of apatite crystals on the thin-ribbon precursor at early stages of porcine enamel mineralization. Calcif Tissue Int 53:249-56
Aoba, T; Shimoda, S; Akita, H et al. (1992) Anti-peptide antibodies reactive with epitopic domains of porcine amelogenins at the C-terminus. Arch Oral Biol 37:249-55
Akita, H; Fukae, M; Shimoda, S et al. (1992) Localization of glycosylated matrix proteins in secretory porcine enamel and their possible functional roles in enamel mineralization. Arch Oral Biol 37:953-62
Aoba, T; Moreno, E C; Shimoda, S (1992) Competitive adsorption of magnesium and calcium ions onto synthetic and biological apatites. Calcif Tissue Int 51:143-50
Aoba, T; Shimoda, S; Shimokawa, H et al. (1992) Common epitopes of mammalian amelogenins at the C-terminus and possible functional roles of the corresponding domain in enamel mineralization. Calcif Tissue Int 51:85-91
McKee, M D; Aoba, T; Moreno, E C (1991) Morphology of the enamel organ in the miniature swine. Anat Rec 230:97-113

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