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      Induction of membrane circular dorsal ruffles requires co-signalling of integrin-ILK-complex and EGF receptor.

      Journal of Cell Science
      Animals, Cell Membrane Structures, enzymology, physiology, Cells, Cultured, Cysteine Endopeptidases, genetics, metabolism, Fibroblasts, Humans, Integrin alpha5beta1, Mice, Mice, Knockout, Phosphorylation, Protein-Serine-Threonine Kinases, Proto-Oncogene Proteins pp60(c-src), Receptor, Epidermal Growth Factor, Signal Transduction, Tyrosine

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          Abstract

          Integrin and receptor tyrosine kinase signalling networks cooperate to regulate various biological functions. The molecular details underlying the integration of both signalling networks remain largely uncharacterized. Here we identify a signalling module composed of a fibronectin-α5β1-integrin-integrin-linked-kinase (ILK) complex that, in concert with epidermal growth factor (EGF) cues, cooperatively controls the formation of transient actin-based circular dorsal ruffles (DRs) in fibroblasts. DR formation depends on the precise spatial activation of Src at focal adhesions by integrin and EGF receptor signals, in an ILK-dependent manner. In a SILAC-based phosphoproteomics screen we identified the tumour-suppressor Cyld as being required for DR formation induced by α5β1 integrin and EGF receptor co-signalling. Furthermore, EGF-induced Cyld tyrosine phosphorylation is controlled by integrin-ILK and Src as a prerequisite for DR formation. This study provides evidence for a novel function of integrin-ILK and EGF signalling crosstalk in mediating Cyld tyrosine phosphorylation and fast actin-based cytoskeletal rearrangements.

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