Cell-cell and cell-substratum adhesive interactions are critical to normal morphogenesis and maitenance of tissue architecture. Alterations in these interactions have been documented in malignant cells and in abnormal development. Using broad spectrum antisera which perturb adhesion in mouse mammary tumor epitherlial cells (MMTE), we have purified a complex of cell-substratum adhesion-related integral membrane glycoproteins of 120-160 Kd (called GP120-160) and an 80 Kd soluble fragment of a 120 Kd cell-cell adhesion-related surface membrane glycoprotein that we have called cell-CAM 120/80. Antisera against these glycoproteins interfere with adhesive interactions of preimplantation mouse embryos as well as MMTE. In this application we propose to (1) produce a bank of specific antisera and monoclonal antibodies against these adhesion glycoproteins that will recognize various regions of these adhesion glycoproteins in their native and denatured forms; (2) localize the adhesion glycoproteins in developing mouse embryos and mature tissue using immunofluorescence and immunoelectron microscopy; (3) characterize the peptide structures, phosphorylation state and oligosaccharide composition of these glycoproteins; (4) study the organization of these glycoproteins in the surface membrane asking in particular whether they are transmembrane and how they interact within the membrane; (5) if the adhesion glycoproteins are transmembrane, determine whether they interact with the cytoskeleton using microinjection of antibodies against adhesion glycoproteins and looking for changes in the distribution of the cytoskeleton; (6) purify a second cell-cell adhesion molecule which we have identified in early mouse embryos, using approaches similar to those we used previously to successfully isolate cell-CAM 120/80 and GP120-160; and (7) clone the genes coding for these glycoproteins. As a result of these studies we will increase significantly our knowledge of how integral membrane glycoproteins mediate cell-cell and cell-substratum interactions in both cultured cells and developing embryos.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA027909-09
Application #
3167886
Study Section
Cognition and Perception Study Section (CP)
Project Start
1980-04-01
Project End
1989-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
9
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Wistar Institute
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Wheelock, M J; Buck, C A; Bechtol, K B et al. (1987) Soluble 80-kd fragment of cell-CAM 120/80 disrupts cell-cell adhesion. J Cell Biochem 34:187-202
Buck, C A; Horwitz, A F (1987) Cell surface receptors for extracellular matrix molecules. Annu Rev Cell Biol 3:179-205
Damsky, C H; Knudsen, K A; Bradley, D et al. (1985) Distribution of the cell substratum attachment (CSAT) antigen on myogenic and fibroblastic cells in culture. J Cell Biol 100:1528-39