The role of membrane microdomains in transmembrane signaling through the epithelial glycoprotein Gp140/CDCP1.

Publication Type:

Journal Article


Biochimica et biophysica acta, Volume 1780, Issue 3, p.486-96 (2008)


2008, Amino Acid Sequence, Antibodies, Monoclonal, Antigens, CD, Basic Sciences Division, beta-Cyclodextrins, Cell Adhesion, Cell Adhesion Molecules, Cell Communication, Cells, Cultured, Center-Authored Paper, Detergents, Epidermis, Epithelial Cells, Humans, KERATINOCYTES, Membrane Microdomains, Models, Biological, Molecular Sequence Data, Neoplasm Proteins, PHOSPHORYLATION, Protein Structure, Tertiary, Protein Transport, Public Health Sciences Division, Signal Transduction, src-Family Kinases, Up-Regulation


Cell adhesion to the extracellular matrix (ECM) via integrin adhesion receptors initiates signaling cascades leading to changes in cell behavior. While integrin clustering is necessary to initiate cell attachment to the matrix, additional membrane components are necessary to mediate the transmembrane signals and the cell adhesion response that alter downstream cell behavior. Many of these signaling components reside in glycosphingolipid-rich and cholesterol-rich membrane domains such as Tetraspanin Enriched Microdomains (TEMs)/Glycosynapse 3 and Detergent-Resistant Microdomains (DRMs), also known as lipid rafts. In the following article, we will review examples of how components in these membrane microdomains modulate integrin adhesion after initial attachment to the ECM. Additionally, we will present data on a novel adhesion-responsive transmembrane glycoprotein Gp140/CUB Domain Containing Protein 1, which clusters in epithelial cell-cell contacts. Gp140 can then be phosphorylated by Src Family Kinases at tyrosine 734 in response to outside-in signals-possibly through interactions involving the extracellular CUB domains. Data presented here suggests that outside-in signals through Gp140 in cell-cell contacts assemble membrane clusters that associate with membrane microdomains to recruit and activate SFKs. Active SFKs then mediate phosphorylation of Gp140, SFK and PKCdelta with Gp140 acting as a transmembrane scaffold for these kinases. We propose that the clustering of Gp140 and signaling components in membrane microdomains in cell-cell contacts contributes to changes in cell behavior.