The goal of this proposal is to test the hypothesis that integrins are involved in the initiation of osteoblast cell differentiation. Our first goal is to determine which alpha-subunit is responsible for initiating the differentiation of osteoblasts. We will continue on-going studies aimed at determining the integrin species expressed during the development of hard tissues in vivo. Once the species of integrin alpha- subunits that are expressed in hard tissues in vivo are known, we will use a series of molecular approaches to determine which integrin alpha- subunit is involved in developmental processes. We will up-regulate the expression of integrin alpha-subunits (a) by the use of integrin expression vectors, and (b) by the isolation of mutant cell lines which are altered in the expression of selected integrins. Second, we will employ agents that selectively inhibit integrin function (synthetic peptides and neutralizing antibodies). Emphasis will be placed on expression vector studies. This series of experiments should lead to the identification of the integrin alpha-subunit that is responsible for the initiation of osteoblast cell differentiation. The studies proposed above are modelled after the myoblast system in which (a) competence for differentiation is determined by the expression of the MyoD gene and (b) initiation of cell differentiation takes place following transmission of an integrin transduced signal. Our second goal is to examine the integrin signal transduction pathway in osteoblasts. We propose to study the effects of ligand-receptor binding upon signal transduction. Second, we will examine a recently described """"""""adhesion plaque"""""""" tyrosine protein kinase system that conveys signals from integrins. third, we will determine the transcription factors that respond to integrin transduced signals. The studies proposed should define the role of integrin signal transduction mechanisms in osteoblast cell differentiation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE008144-07
Application #
2129966
Study Section
Physiological Sciences Study Section (PSF)
Project Start
1988-07-01
Project End
1997-06-30
Budget Start
1995-07-01
Budget End
1996-06-30
Support Year
7
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Anatomy/Cell Biology
Type
Other Domestic Higher Education
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Giambernardi, T A; Sakaguchi, A Y; Gluhak, J et al. (2001) Neutrophil collagenase (MMP-8) is expressed during early development in neural crest cells as well as in adult melanoma cells. Matrix Biol 20:577-87
Giambernardi, T A; Klebe, R J (2000) Relative reverse transcription-polymerase chain reaction. Methods Mol Biol 137:51-8
Klebe, R J; Rodriguez, S A; VerBeek, M L et al. (1999) Simple method for ""hot-starting"" RT-PCR. Biotechniques 27:1108-10
Grant, G M; Giambernardi, T A; Grant, A M et al. (1999) Overview of expression of matrix metalloproteinases (MMP-17, MMP-18, and MMP-20) in cultured human cells. Matrix Biol 18:145-8
Taylor, G P; Troyer, D A; Giambernardi, T A et al. (1998) Extraction of RNA from single frozen sections. J Pathol 184:332-5
Giambernardi, T A; Grant, G M; Taylor, G P et al. (1998) Overview of matrix metalloproteinase expression in cultured human cells. Matrix Biol 16:483-96
Giambernardi, T A; Rodeck, U; Klebe, R J (1998) Bovine serum albumin reverses inhibition of RT-PCR by melanin. Biotechniques 25:564-6
Giambernardi, T A; Klebe, R J (1997) Use of oxygen-permeable silicone rubber pouches for growing mass cultures of bacteria. Lett Appl Microbiol 24:207-10
Garcia, M A; Klebe, R J (1997) Affinity chromatography of RNase inhibitor. Mol Biol Rep 24:231-3
Klebe, R J; Grant, G M; Grant, A M et al. (1996) RT-PCR without RNA isolation. Biotechniques 21:1094-100

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