The ultimate goal of this work is to understand how tissue interactions control differentiated cell behavior. These interactions are mediated by cell surface receptors. On epithelial cells, these receptors interact with the; extracellular matrix (ECM), as well as with adjacent cell surfaces, to provide anchorage and establish the high degree of polarity that characterizes differentiated epithelial cells. The ligands for these receptors are topically large and multivalent, forming an insoluble scaffolding that immobilizes the receptor and is likely to convey information to the cell. The information may be interpreted via cytoskeletal organization leading to specific cell shape. In addition failure to anchor the receptor may allow its loss from the surface by internalization, conveying a signal to the interior of the cell. A cell surface proteoglycan (syndecan) of epithelial cells binds a variety of matrix ligands, is anchored to the cytoskeleton and exhibits variable life-times at the cell surface. In addition, its ability to recognize its ligands may be modified by alterations in its structure during synthesis. This proposal is to study the mechanisms that promote the anchorage of syndecan to the ECM and cytoskeleton, understand why its structure changes with cell behavior and identify the reason for its sorting when removed from the cell surface. An understanding of the molecules and mechanisms that allow external interactions of cells to be recognized, translated, and transmitted across the plasma membrane to the cytoplasm is required to develop rational means of preventing the abnormalities in organ morphogenesis and cell behavior that lead to diseases and birth defects.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
2R01HD021881-05
Application #
3321004
Study Section
Pathobiochemistry Study Section (PBC)
Project Start
1985-09-01
Project End
1994-03-31
Budget Start
1989-07-01
Budget End
1990-03-31
Support Year
5
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
McQuade, Kyle J; Rapraeger, Alan C (2003) Syndecan-1 transmembrane and extracellular domains have unique and distinct roles in cell spreading. J Biol Chem 278:46607-15
Burbach, Brandon J; Friedl, Andreas; Mundhenke, Christoph et al. (2003) Syndecan-1 accumulates in lysosomes of poorly differentiated breast carcinoma cells. Matrix Biol 22:163-77
Beauvais, DeannaLee M; Rapraeger, Alan C (2003) Syndecan-1-mediated cell spreading requires signaling by alphavbeta3 integrins in human breast carcinoma cells. Exp Cell Res 286:219-32
Rapraeger, Alan C (2002) Heparan sulfate-growth factor interactions. Methods Cell Biol 69:83-109