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Dentin sialoprotein and dentin phosphoprotein overexpression during amelogenesis.
Michael L Paine1, Wen Luo, Hong-Jun Wang
1University of Southern California, School of Dentistry, Center for Craniofacial Molecular Biology, Los Angeles, California 90033, USA. paine@usc.edu
The Journal of Biological Chemistry
|July 15, 2005
Summary
Dentin sialophosphoprotein yields two proteins, dentin sialoprotein and dentin phosphoprotein, crucial for tooth enamel formation. Overexpressing dentin sialoprotein enhances mineralization, while dentin phosphoprotein causes defective enamel.
Area of Science:
- Biochemistry
- Developmental Biology
- Materials Science
Background:
- Dentin sialophosphoprotein (DSPP) gene produces a single protein, post-translationally modified into dentin sialoprotein (DSP) and dentin phosphoprotein (DPP).
- DSPP is primarily expressed by odontoblasts but also transiently by presecretory ameloblasts, suggesting a role in early amelogenesis and the dentino-enamel junction (DEJ).
Purpose of the Study:
- To investigate the distinct functions of DSP and DPP during amelogenesis using a transgenic animal model.
- To elucidate the contribution of DSPP to the formation and properties of the DEJ and aprismatic enamel.
Main Methods:
- Generation of transgenic animals with extended expression of DSP or DPP throughout amelogenesis.
- Analysis of enamel mineralization, morphology, thickness, hardness, and wear resistance in wild-type and transgenic mice.
Main Results:
- Overexpression of DSP led to increased enamel mineralization without significant morphological changes.
- DSP inclusion in aprismatic enamel correlated with increased hardness compared to bulk enamel.
- Overexpression of DPP resulted in pitted, chalky enamel with non-uniform thickness, increased wear, and disrupted prismatic structure.
Conclusions:
- DSP and DPP possess distinct functions in tooth formation.
- DSP contributes to enamel mineralization and hardness, particularly in aprismatic enamel.
- DPP plays a critical role in proper enamel structure and integrity; its disruption leads to defective enamel properties.
- The DEJ is a unique transitional zone, and DSPP proteins expressed by presecretory ameloblasts contribute to its distinct properties.