| Literature DB >> 19407150 |
J Hatakeyama1, S Fukumoto, T Nakamura, N Haruyama, S Suzuki, Y Hatakeyama, L Shum, C W Gibson, Y Yamada, A B Kulkarni.
Abstract
Amelogenin and ameloblastin, the major enamel matrix proteins, are important for enamel mineralization. To identify their synergistic roles in enamel development, we generated Amel X(-/-)/Ambn(-/-) mice. These mice showed additional enamel defects in comparison with Amel X(-/-) or Ambn(-/-) mice. In 7-day-old Amel X(-/-)/Ambn(-/-) mice, not only was the ameloblast layer irregular and detached from the enamel surface, as in Ambn(-/-), but also, the enamel width was significantly reduced in the double-null mice as compared with Amel X(-/-) or Ambn(-/-) mice. Proteomic analysis of the double-null teeth revealed increased levels of RhoGDI (Arhgdia), a Rho-family-specific guanine nucleotide dissociation inhibitor, which is involved in important cellular processes, such as cell attachment. Both Amel X(-/-)/Ambn(-/-) mice and Ambn(-/-) mice displayed positive staining with RhoGDI antibody in the irregularly shaped ameloblasts detached from the matrix. Ameloblastin-regulated expression of RhoGDI suggests that Rho-mediated signaling pathway might play a role in enamel formation.Entities:
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Year: 2009 PMID: 19407150 PMCID: PMC2758615 DOI: 10.1177/0022034509334749
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116