The inositol phosphatase SHIP2 enables sustained ERK activation downstream of FGF receptors by recruiting Src kinases
Jazyk angličtina Země Spojené státy americké Médium electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
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-zdroje
- MeSH
- adaptorové proteiny signální transdukční genetika metabolismus MeSH
- aktivace enzymů MeSH
- extracelulárním signálem regulované MAP kinasy genetika metabolismus MeSH
- fosfatidylinositol-3,4,5-trisfosfát-5-fosfatasy genetika metabolismus MeSH
- fosforylace MeSH
- HEK293 buňky MeSH
- lidé MeSH
- MAP kinasový signální systém * MeSH
- membránové proteiny genetika metabolismus MeSH
- nádorové buněčné linie MeSH
- receptory fibroblastových růstových faktorů genetika metabolismus MeSH
- skupina kinas odvozených od src-genu genetika metabolismus MeSH
- tyrosinfosfatasa nereceptorového typu 11 genetika metabolismus MeSH
- vazba proteinů MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- adaptorové proteiny signální transdukční MeSH
- extracelulárním signálem regulované MAP kinasy MeSH
- fosfatidylinositol-3,4,5-trisfosfát-5-fosfatasy MeSH
- FRS2 protein, human MeSH Prohlížeč
- INPPL1 protein, human MeSH Prohlížeč
- membránové proteiny MeSH
- PTPN11 protein, human MeSH Prohlížeč
- receptory fibroblastových růstových faktorů MeSH
- skupina kinas odvozených od src-genu MeSH
- tyrosinfosfatasa nereceptorového typu 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
Citace poskytuje Crossref.org
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