During tooth development, cells of Hertwig's epithelial root sheath secrete enamel matrix proteins. A purified enamel matrix product (Enamel Matrix Derivative, EMD) from developing porcine teeth became commercially available and has been successfully employed to restore fully functional periodontal ligament, cementum and alveolar bone. The regenerative capacity of EMD has been demonstrated in clinical and animal studies. However the biological mechanisms are not known. We hypothesize that EMD regulates some primary gene expression, which regulate osteoblast differentiation, growth and function. The objective of this project is to identify the genes regulated in the EMD treated preosteoblastic cell line MC3T3-E1 and MG63 osteoblast-like cells using DNA microarray technology. Identified interesting genes will be confirmed by northern blot analysis. Finding the common gene changes in both cell lines will help us to find which genes are involved in the interaction between EMD and osteoblasts. The difference of EMD regulated gene changes between the two cell lines will help us to understand why EMD have different effects on preosteoblasts and osteoblast-like cells. We believe that, at the completion of the proposed research, our findings will constitute sufficient data for a future R01 grant application to investigate the EMD regulated genes and the relationship of these genes with osteoblast growth and function. The results of this application will also provide foundation for identifying what molecules might be active in EMD to regulate the identified genes. The identified molecules in the EMD could be used more efficiently and conveniently for periodontal regeneration than the isolated EMD protein mixture.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Small Research Grants (R03)
Project #
5R03DE014126-02
Application #
6626046
Study Section
NIDCR Special Grants Review Committee (DSR)
Program Officer
Small, Rochelle K
Project Start
2002-03-01
Project End
2004-02-28
Budget Start
2003-03-01
Budget End
2004-02-28
Support Year
2
Fiscal Year
2003
Total Cost
$72,500
Indirect Cost
Name
University of Connecticut
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
022254226
City
Farmington
State
CT
Country
United States
Zip Code
06030
He, Jianing; King, Yiming; Jiang, Jin et al. (2005) Enamel matrix derivative inhibits TNF-alpha-induced apoptosis in osteoblastic MC3T3-E1 cells. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 99:761-7
He, Jianing; Jiang, Jin; Safavi, Kamran E et al. (2004) Emdogain promotes osteoblast proliferation and differentiation and stimulates osteoprotegerin expression. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 97:239-45
He, Jianing; Jiang, Jin; Safavi, Kamran E et al. (2004) Direct contact between enamel matrix derivative (EMD) and osteoblasts is not required for EMD-induced cell proliferation. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 98:370-5