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MenaINV mediates synergistic cross-talk between signaling pathways driving chemotaxis and haptotaxis.
- Source :
-
Molecular biology of the cell [Mol Biol Cell] 2016 Oct 15; Vol. 27 (20), pp. 3085-3094. Date of Electronic Publication: 2016 Aug 24. - Publication Year :
- 2016
-
Abstract
- Directed cell migration, a key process in metastasis, arises from the combined influence of multiple processes, including chemotaxis-the directional movement of cells to soluble cues-and haptotaxis-the migration of cells on gradients of substrate-bound factors. However, it is unclear how chemotactic and haptotactic pathways integrate with each other to drive overall cell behavior. Mena <superscript>INV</superscript> has been implicated in metastasis by driving chemotaxis via dysregulation of phosphatase PTP1B and more recently in haptotaxis via interaction with integrin α5β1. Here we find that Mena <superscript>INV</superscript> -driven haptotaxis on fibronectin (FN) gradients requires intact signaling between α5β1 integrin and the epidermal growth factor receptor (EGFR), which is influenced by PTP1B. Furthermore, we show that Mena <superscript>INV</superscript> -driven haptotaxis and ECM reorganization both require the Rab-coupling protein RCP, which mediates α5β1 and EGFR recycling. Finally, Mena <superscript>INV</superscript> promotes synergistic migratory response to combined EGF and FN in vitro and in vivo, leading to hyperinvasive phenotypes. Together our data demonstrate that Mena <superscript>INV</superscript> is a shared component of multiple prometastatic pathways that amplifies their combined effects, promoting synergistic cross-talk between RTKs and integrins.<br /> (© 2016 Oudin et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).)
- Subjects :
- Animals
Cell Adhesion Molecules metabolism
Cell Movement physiology
Cytoskeletal Proteins physiology
ErbB Receptors metabolism
Integrin alpha5beta1 metabolism
Integrins
Mice
Microfilament Proteins metabolism
Neoplasm Metastasis physiopathology
Phosphoproteins metabolism
Protein Tyrosine Phosphatase, Non-Receptor Type 1 metabolism
Receptor Cross-Talk
Receptor Protein-Tyrosine Kinases metabolism
Signal Transduction physiology
Tumor Cells, Cultured
Chemotaxis physiology
Cytoskeletal Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1939-4586
- Volume :
- 27
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- Molecular biology of the cell
- Publication Type :
- Academic Journal
- Accession number :
- 27559126
- Full Text :
- https://doi.org/10.1091/mbc.E16-04-0212