The overall objective of this Program Project is to provide new and fundamental information on how nature controls mineralization in developing mineralized tissues, like enamel, using amelogenesis as a model. Our overall working hypothesis is that the formation of the highly organized enamel tissue results from genetically-controlled processes involving: cell motility, mineral ion fluxes; the secretion, self assembly and processing of matrix proteins, and the subsequent control of nucleation and crystal growth by specialized proteins coupled with the cell-controlled establishment of inherent driving forces to support mineralization. Specifically, we propose to elucidate fundamental mechanisms which control enamel formation through integrated studies on: 1). matrix protein-mineral interactions in the control of crystal nucleation and crystal growth; 2) the cellular (ameloblast) control of mineral ion transport, extracellular mineral ion composition, pH. and the driving force for mineral deposition; 3) the role of specific protein-protein interactions in the control of mineralization; 4) the control of protein function and mineralization via the processing of enamel-matrix proteins by tissue-specific proteinases; and 5) cell (ameloblast)-cell interactions and cell-matrix interactions, leading to the control of cell motility and enamel patterning. These studies will be carried out through the integration of five independent projects facilitated by a Protein Core, which will generate recombinant enamel proteins in both bacteria and eukaryotic cell expression systems. These areas of research will be addressed in a multi-disciplinary fashion using state-of-the-art techniques (e.g. the yeast two-hybrid system; PCR-based homology cloning, atomic force microscopy, confocal microscopy and direct 3-D fluorescence microscopy; SEM and TEM; immunohistochemistry) and physiochemical considerations to address the overall mechanisms of enamel formation. Long term, this information will be useful in: 1) the design of new methodologies for the preparation of biomaterials with specific desirable properties; 2) the diagnosis and prevention of diseases mineralized tissues through genetic means; and 3) the design of procedures for the regeneration of damaged and diseases mineralized tissues.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Program Projects (P01)
Project #
1P01DE013237-01
Application #
2849036
Study Section
Special Emphasis Panel (ZDE1-GH (30))
Project Start
1999-08-01
Project End
2004-07-31
Budget Start
1999-08-01
Budget End
2000-07-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Forsyth Institute
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02142
Hermo, Louis; Chung, Shari; Gregory, Mary et al. (2008) Alterations in the testis of hormone sensitive lipase-deficient mice is associated with decreased sperm counts, sperm motility, and fertility. Mol Reprod Dev 75:565-77
Primiani, Nadia; Gregory, Mary; Dufresne, Julie et al. (2007) Microvillar size and espin expression in principal cells of the adult rat epididymis are regulated by androgens. J Androl 28:659-69
Hermo, Louis; Korah, Nadine; Gregory, Mary et al. (2007) Structural alterations of epididymal epithelial cells in cathepsin A-deficient mice affect the blood-epididymal barrier and lead to altered sperm motility. J Androl 28:784-97
Khatchadourian, Karine; Smith, Charles E; Metzler, Martina et al. (2007) Structural abnormalities in spermatids together with reduced sperm counts and motility underlie the reproductive defect in HIP1-/- mice. Mol Reprod Dev 74:341-59
Margolis, H C; Beniash, E; Fowler, C E (2006) Role of macromolecular assembly of enamel matrix proteins in enamel formation. J Dent Res 85:775-93
Turk, Benjamin E; Lee, Daniel H; Yamakoshi, Yasuo et al. (2006) MMP-20 is predominately a tooth-specific enzyme with a deep catalytic pocket that hydrolyzes type V collagen. Biochemistry 45:3863-74
Smith, Charles E; Nanci, Antonio; Moffatt, Pierre (2006) Evidence by signal peptide trap technology for the expression of carbonic anhydrase 6 in rat incisor enamel organs. Eur J Oral Sci 114 Suppl 1:147-53; discussion 164-5, 380-1
Fowler, Christabel E; Beniash, Elia; Yamakoshi, Yasuo et al. (2006) Co-operative mineralization and protein self-assembly in amelogenesis: silica mineralization and assembly of recombinant amelogenins in vitro. Eur J Oral Sci 114 Suppl 1:297-303; discussion 327-9, 382
Ruz, Ricardo; Gregory, Mary; Smith, Charles E et al. (2006) Expression of aquaporins in the efferent ductules, sperm counts, and sperm motility in estrogen receptor-alpha deficient mice fed lab chow versus casein. Mol Reprod Dev 73:226-37
Aichmayer, B; Margolis, H C; Sigel, R et al. (2005) The onset of amelogenin nanosphere aggregation studied by small-angle X-ray scattering and dynamic light scattering. J Struct Biol 151:239-49

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