The collagen receptor DDR1 regulates cell spreading and motility by associating with myosin IIA
doi: 10.1242/jcs.046219
pmid: 19401332
The collagen receptor DDR1 regulates cell spreading and motility by associating with myosin IIA
The spreading and migration of cells on adhesive substrates is regulated by the counterbalance of contractile and protrusive forces. Non-muscle myosin IIA, an ubiquitously expressed contractile protein and enzyme, is implicated in the regulation of cell spreading and directional migration in response to various stimuli. Here we show that discoidin domain receptor 1 (DDR1), a tyrosine kinase receptor activated by type I collagen, associates with the non-muscle myosin IIA heavy chain (NMHC-IIA) upon ligand stimulation. An association was also indicated by coimmunoprecipitation of NMHC-IIA with full-length DDR1, but not with the truncated DDR1d-isoform lacking the kinase domain. DDR1 was important for assembly of NMHC-IIA into filaments on cells plated on collagen. DDR1 expression inhibited cell spreading over collagen but promoted cell migration. By contrast, blockade of non-muscle myosin II activity by blebbistatin enhanced cell spreading but inhibited migration over collagen. We propose that myosin and DDR1 impact cell spreading and migration by regulating adhesive contacts with collagen.
- Canadian Institutes of Health Research Canada
- University of Toronto Canada
Mice, Knockout, Myosin Heavy Chains, Molecular Motor Proteins, Nonmuscle Myosin Type IIA, Receptor Protein-Tyrosine Kinases, Heterocyclic Compounds, 4 or More Rings, Collagen Type I, Actin Cytoskeleton, Mice, Protein Transport, Discoidin Domain Receptor 1, Cell Movement, Cell Line, Tumor, Mutation, Cell Adhesion, NIH 3T3 Cells, Animals, Humans, Cell Shape, Protein Binding
Mice, Knockout, Myosin Heavy Chains, Molecular Motor Proteins, Nonmuscle Myosin Type IIA, Receptor Protein-Tyrosine Kinases, Heterocyclic Compounds, 4 or More Rings, Collagen Type I, Actin Cytoskeleton, Mice, Protein Transport, Discoidin Domain Receptor 1, Cell Movement, Cell Line, Tumor, Mutation, Cell Adhesion, NIH 3T3 Cells, Animals, Humans, Cell Shape, Protein Binding
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