The inositol phosphatase SHIP2 enables sustained ERK activation downstream of FGF receptors by recruiting Src kinases
Language English Country United States Media electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R01 AR066124
NIAMS NIH HHS - United States
R01 AR062651
NIAMS NIH HHS - United States
PubMed
30228226
DOI
10.1126/scisignal.aap8608
PII: 11/548/eaap8608
Knihovny.cz E-resources
- MeSH
- Adaptor Proteins, Signal Transducing genetics metabolism MeSH
- Enzyme Activation MeSH
- Extracellular Signal-Regulated MAP Kinases genetics metabolism MeSH
- Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases genetics metabolism MeSH
- Phosphorylation MeSH
- HEK293 Cells MeSH
- Humans MeSH
- MAP Kinase Signaling System * MeSH
- Membrane Proteins genetics metabolism MeSH
- Cell Line, Tumor MeSH
- Receptors, Fibroblast Growth Factor genetics metabolism MeSH
- src-Family Kinases genetics metabolism MeSH
- Protein Tyrosine Phosphatase, Non-Receptor Type 11 genetics metabolism MeSH
- Protein Binding MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- Adaptor Proteins, Signal Transducing MeSH
- Extracellular Signal-Regulated MAP Kinases MeSH
- Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases MeSH
- FRS2 protein, human MeSH Browser
- INPPL1 protein, human MeSH Browser
- Membrane Proteins MeSH
- PTPN11 protein, human MeSH Browser
- Receptors, Fibroblast Growth Factor MeSH
- src-Family Kinases MeSH
- Protein Tyrosine Phosphatase, Non-Receptor Type 11 MeSH
Sustained activation of extracellular signal-regulated kinase (ERK) drives pathologies caused by mutations in fibroblast growth factor receptors (FGFRs). We previously identified the inositol phosphatase SHIP2 (also known as INPPL1) as an FGFR-interacting protein and a target of the tyrosine kinase activities of FGFR1, FGFR3, and FGFR4. We report that loss of SHIP2 converted FGF-mediated sustained ERK activation into a transient signal and rescued cell phenotypes triggered by pathologic FGFR-ERK signaling. Mutant forms of SHIP2 lacking phosphoinositide phosphatase activity still associated with FGFRs and did not prevent FGF-induced sustained ERK activation, demonstrating that the adaptor rather than the catalytic activity of SHIP2 was required. SHIP2 recruited Src family kinases to the FGFRs, which promoted FGFR-mediated phosphorylation and assembly of protein complexes that relayed signaling to ERK. SHIP2 interacted with FGFRs, was phosphorylated by active FGFRs, and promoted FGFR-ERK signaling at the level of phosphorylation of the adaptor FRS2 and recruitment of the tyrosine phosphatase PTPN11. Thus, SHIP2 is an essential component of canonical FGF-FGFR signal transduction and a potential therapeutic target in FGFR-related disorders.
Central European Institute of Technology Masaryk University 62500 Brno Czech Republic
Department of Biology Masaryk University 62500 Brno Czech Republic
Department of Human Genetics University of California Los Angeles CA 90095 USA
Department of Orthopedic Surgery University of California Los Angeles CA 90095 USA
Department of Tumor Biology Institute for Cancer Research Norwegian Radium Hospital 0379 Oslo Norway
Institute of Clinical Medicine Faculty of Medicine University of Oslo 0379 Oslo Norway
International Clinical Research Center St Anne's University Hospital 65691 Brno Czech Republic
References provided by Crossref.org
Specific inhibition of fibroblast growth factor receptor 1 signaling by a DNA aptamer
Ligand bias underlies differential signaling of multiple FGFs via FGFR1