The University of Pennsylvania Research Center in Oral Biology is a broadly based multidisciplinary institute involving scientists mainly in the School of Dental Medicine but in which members of the Schools of Medicine and Veterinary Medicine also participate. the fundamental aim of the Center is to provide the setting and resources for scientists in a variety of disciplines to apply the latest scientific and technological advances to challenging oral health problems. The research program is organized under two major areas: (1) The Molecular and Cellular Biology of Oral Pathogens, (2) The Molecular and Cellular Biology of Mineralized Tissues. Included in the program are 4 research projects, and 2 supporting Cores. The problems under investigation range from studies on the molecular mechanisms involved in the pathogenesis or oral infections to delineation of the factors responsible for the differentiation of cells in mineralizing tissues. Specifically, we are continuing fundamental studies on the glycoproteins of Herpes Simplex virus, which remains a major public health problem, causing widespread morbidity and, because of its oncogenic potential, possibly even mortality. Center studies have led to clinical trials of a promising subunit vaccine based on glycoprotein gD. In the oral cavity, the aggregation of bacteria and their clearance or alternatively their colonization on tooth surfaces plays a central role in the initiation of both dental caries and periodontal disease. To understand the mechanisms of these interactions, detailed studies of the binding of streptococci through a surface receptor protein (that has been cloned) to a salivary agglutinin are being carried out. Progressive tissue destruction is the hallmark of periodontal disease, and studies continue on the fundamental mechanisms whereby the leukotoxin of Actinobacillus actinomycetemcomitans, a likely candidate as a major periodontal pathogen, kills host cells. During tooth formation, ameloblasts secrete proteins which are involved in mineralization of the enamel layer. Center scientists have cloned the genes encoding the major class of enamel protein, amelogenins, and studies are planned, using recombinantly expressed proteins, to determine their role in the formation of the unique hydroxyapatite crystals found in the developing enamel matrix. Many of these studies involved collaboration between scientists in the Center and also with other scientists within and outside the University. In addition to its research function, the Center serves as a resource for the training of undergraduate and graduate dental students, undergraduates in the College and Ph.D. candidates in the biological sciences.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Specialized Center (P50)
Project #
5P50DE008239-08
Application #
2130020
Study Section
Special Emphasis Panel (SRC (10))
Project Start
1987-12-01
Project End
1997-11-30
Budget Start
1994-12-01
Budget End
1995-11-30
Support Year
8
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Biology
Type
Schools of Dentistry
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Peng, T; Ponce-de-Leon, M; Jiang, H et al. (1998) The gH-gL complex of herpes simplex virus (HSV) stimulates neutralizing antibody and protects mice against HSV type 1 challenge. J Virol 72:65-72
Bashir, M M; Abrams, W R; Tucker, T et al. (1998) Molecular cloning and characterization of the bovine and human tuftelin genes. Connect Tissue Res 39:13-24;discussion 63-7
Karakelian, D; Lear, J D; Lally, E T et al. (1998) Characterization of Actinobacillus actinomycetemcomitans leukotoxin pore formation in HL60 cells. Biochim Biophys Acta 1406:175-87
Taichman, N S; Cruchley, A T; Fletcher, L M et al. (1998) Vascular endothelial growth factor in normal human salivary glands and saliva: a possible role in the maintenance of mucosal homeostasis. Lab Invest 78:869-75
Peng, T; Ponce de Leon, M; Novotny, M J et al. (1998) Structural and antigenic analysis of a truncated form of the herpes simplex virus glycoprotein gH-gL complex. J Virol 72:6092-103
Jenkinson, H F; Demuth, D R (1997) Structure, function and immunogenicity of streptococcal antigen I/II polypeptides. Mol Microbiol 23:183-90
Lally, E T; Kieba, I R; Sato, A et al. (1997) RTX toxins recognize a beta2 integrin on the surface of human target cells. J Biol Chem 272:30463-9
Whitbeck, J C; Peng, C; Lou, H et al. (1997) Glycoprotein D of herpes simplex virus (HSV) binds directly to HVEM, a member of the tumor necrosis factor receptor superfamily and a mediator of HSV entry. J Virol 71:6083-93
Brooks, W; Demuth, D R; Gil, S et al. (1997) Identification of a Streptococcus gordonii SspB domain that mediates adhesion to Porphyromonas gingivalis. Infect Immun 65:3753-8
Demuth, D R; Duan, Y; Jenkinson, H F et al. (1997) Interruption of the Streptococcus gordonii M5 sspA/sspB intergenic region by an insertion sequence related to IS1167 of Streptococcus pneumoniae. Microbiology 143 ( Pt 6):2047-55

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