Cell-cell adhesion plays a central role in a variety of developmental events, particularly in the establishment of the nervous system. Moreover, recent studies indicate that alterations in the expression of cell adhesion molecules(CAMs) accompany a number of pathological states. Since our demonstration that the neural cell adhesion molecule, N-CAM, contains five segments resembling the structural domains of immunoglobulins and two other segments that are similar to the type III repeats of the substrate adhesion molecule fibronectin, these structural features have been found in other CAMs. The chicken molecules Nr-CAM, Ng-CAM, and neurofascin and the rodent proteins L1/NILE and ankyrin binding glycoprotein constitute a subfamily of such CAMs in the nervous system: each of these distinct cell surface proteins has six immunoglobulin-like domains and five fibronectin-like repeats, and they are similar to each other in amino acid sequence. Moreover all of these molecules are expressed on neurons and appear to be important in the outgrowth and fasciculation of neurites. This group of CAMs could thus provide a basis for establishing neuronal pathways. The goal of this project is to define the properties of this subfamily and its role in neural development using Nr-CAM as the paradigm. Nr-CAM binds neurons to each other and binds neurons to fibroblasts by different mechanisms. Each of these activities will be examined in detail and the binding regions localized in the linear structure of the molecule using chemical, molecular biological and cell biological techniques. Features in Nr-CAM that are shared by other proteins in the subfamily will be analyzed for their role in Nr-CAM function. cDNA screening methods will be used to identify new members of this subfamily and to estimate the size of this group of proteins. Together these studies should provide a basis for defining the activities of proteins that are important in the development of the nervous system, and that are likely to play critical roles in a variety of processes such as nerve regeneration and in neurological diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS028932-05A1
Application #
2267297
Study Section
Neurology C Study Section (NEUC)
Project Start
1990-08-01
Project End
1998-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Cunningham, B A (1995) Cell adhesion molecules as morphoregulators. Curr Opin Cell Biol 7:628-33
Krushel, L A; Prieto, A L; Cunningham, B A et al. (1993) Expression patterns of the cell adhesion molecule Nr-CAM during histogenesis of the chick nervous system. Neuroscience 53:797-812
Mauro, V P; Krushel, L A; Cunningham, B A et al. (1992) Homophilic and heterophilic binding activities of Nr-CAM, a nervous system cell adhesion molecule. J Cell Biol 119:191-202
Grumet, M; Mauro, V; Burgoon, M P et al. (1991) Structure of a new nervous system glycoprotein, Nr-CAM, and its relationship to subgroups of neural cell adhesion molecules. J Cell Biol 113:1399-412