The NH2-terminal and COOH-terminal Fragments of Dentin Matrix Protein 1 (DMP1) Localize Differently in the Compartments of Dentin and Growth Plate of Bone

• Published in: The journal of histochemistry and cytochemistry Vol. 57; no. 2; pp. 155 - 166
• Main Authors: Maciejewska, Izabela, Cowan, Cameron, Svoboda, Kathy, Butler, William T, D'Souza, Rena, Qin, Chunlin
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA Histochemical Soc 01.02.2009; SAGE Publications; Histochemical Society
• Subjects: Animals; Animals, Newborn; Cattle; Dentin - growth & development; Dentin - metabolism; Extracellular Matrix Proteins - metabolism; Fluorescence Resonance Energy Transfer; Growth Plate - growth & development; Growth Plate - metabolism; Immunohistochemistry; Microscopy, Confocal; Molar - growth & development; Molar - metabolism; Organ Specificity; Phosphoproteins - metabolism; Rats; Rats, Sprague-Dawley; dentin matrix protein 1; dentinogenesis; osteogenesis; immunolocalization; Forster resonance energy transfer
• DOI: 10.1369/jhc.2008.952630
• ISSN: 0022-1554

Multiple studies have shown that dentin matrix protein 1 (DMP1) is essential for bone and dentin mineralization. After post-translational proteolytic cleavage, DMP1 exists within the extracellular matrix of bone and dentin as an NH2-terminal fragment, a COOH-terminal fragment, and the proteoglycan form of the NH2-terminal fragment (DMP1-PG). To begin to assess the biological function of each fragment, we evaluated the distribution of both fragments in the rat tooth and bone using antibodies specific to the NH2-terminal and COOH-terminal regions of DMP1 and confocal microscopy. In rat first molar organs, the NH2-terminal fragment localized to predentin, whereas the COOH-terminal fragment was mainly restricted to mineralized dentin. In the growth plate of bone, the NH2-terminal fragment appeared in the proliferation and hypertrophic zones, whereas the COOH-terminal fragment occupied the ossification zone. Forster resonance energy transfer analysis showed colocalization of both fragments of DMP1 in odontoblasts and predentin, as well as hypertrophic chondrocytes within the growth plates of bone. The biochemical analysis of bovine teeth showed that predentin is rich in DMP1-PG, whereas mineralized dentin primarily contains the COOH-terminal fragment. We conclude that the differential patterns of expression of NH2-terminal and COOH-terminal fragments of DMP1 reflect their potentially distinct roles in the biomineralization of dentin and bone matrices.