Dentin sialoprotein, dentin phosphoprotein, enamelysin and ameloblastin, tooth- specific molecules that are distinctively expressed during murine dental differentiation
TL;DR: The interrelated expression profiles found for these tooth-specific molecules illustrate the importance of a specific molecular network to initiate highly regulated processes such as cytodifferentiation and the subsequent mineralization.
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Abstract: Dentin sialophosphoprotein [designated DSPP and cleaved into dentin sialoprotein (DSP) and dentin phosphoprotein (DPP)], enamelysin and ameloblastin are each expressed in unique fashions during tooth development. It is possible that these components participate in cell differentiation and the conversion of unmineralized matrix into mineralized structures. In order to delineate the timing and the positioning of these three molecules in a physiological context, we compared their expression profiles by performing in situ hybridization experiments on consecutive sections in developing mouse tissues. Hybridization signals were uniquely detected for DSPP mRNA in odontoblasts and preameloblasts, for enamelysin mRNA in odontoblasts and in the facing ameloblast layer, and for ameloblastin mRNA in preodontoblasts, polarizing odontoblasts and ameloblasts. Immunohistochemistry showed that DSP and ameloblastin transcripts were translated into proteins that were deposited at the apical pole of the differentiated cells (odontoblasts and ameloblasts, respectively). The interrelated expression profiles found for these tooth-specific molecules illustrate the importance of a specific molecular network to initiate highly regulated processes such as cytodifferentiation and the subsequent mineralization.
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Dentin sialophosphoprotein in biomineralization
TL;DR: This review summarizes the important and new developments made in the past four decades regarding the structure and regulation of the Dspp gene, the biochemical characteristics of DSPP, DPP, and DSP as well as the cell/tissue localizations and functions of these molecules.
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A hydrogel scaffold that maintains viability and supports differentiation of dental pulp stem cells
TL;DR: The compatibility of Puramatrix™ with dental pulp stem cell (DPSC) growth and differentiation suggests that self-assembling peptide hydrogels might be useful injectable scaffolds for stem cell-based Regenerative Endodontics.
169
Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization
M. Helen Rajpar,Martin J. Koch,Robin M. Davies,Kieran T. Mellody,Cay M. Kielty,Michael J. Dixon +5 more
TL;DR: Biochemical analysis has demonstrated that this mutation in the DSPP gene causes a failure of translocation of the encoded proteins into the endoplasmic reticulum, and is therefore likely to lead to a loss of function of both dentine sialoprotein and dentine phosphoprotein.
Genes and Related Proteins Involved in Amelogenesis Imperfecta
TL;DR: Current knowledge on the candidate genes involved in amelogenesis imperfecta and the proteins derived from them are reviewed, and current knowledge on their structure, localization within the tissue, and correlation with the various types of this disorder is reviewed.
165
3. Protein-protein interactions of the developing enamel matrix.
John D. Bartlett,Bernhard Ganss,Michel Goldberg,Janet Moradian-Oldak,Michael L. Paine,Malcolm L. Snead,Xin Wen,Shane N. White,Yan Zhou +8 more
TL;DR: The scope of this review is to discuss the current understanding of protein-protein interactions of the developing enamel matrix, and relate this knowledge to enamel biomineralization.
153
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