Nejvíce citovaný článek - PubMed ID 28631381
Tyrosine Kinase Expressed in Hepatocellular Carcinoma, TEC, Controls Pluripotency and Early Cell Fate Decisions of Human Pluripotent Stem Cells via Regulation of Fibroblast Growth Factor-2 Secretion
Cilia project from almost every cell integrating extracellular cues with signaling pathways. Constitutive activation of FGFR3 signaling produces the skeletal disorders achondroplasia (ACH) and thanatophoric dysplasia (TD), but many of the molecular mechanisms underlying these phenotypes remain unresolved. Here, we report in vivo evidence for significantly shortened primary cilia in ACH and TD cartilage growth plates. Using in vivo and in vitro methodologies, our data demonstrate that transient versus sustained activation of FGF signaling correlated with different cilia consequences. Transient FGF pathway activation elongated cilia, while sustained activity shortened cilia. FGF signaling extended primary cilia via ERK MAP kinase and mTORC2 signaling, but not through mTORC1. Employing a GFP-tagged IFT20 construct to measure intraflagellar (IFT) speed in cilia, we showed that FGF signaling affected IFT velocities, as well as modulating cilia-based Hedgehog signaling. Our data integrate primary cilia into canonical FGF signal transduction and uncover a FGF-cilia pathway that needs consideration when elucidating the mechanisms of physiological and pathological FGFR function, or in the development of FGFR therapeutics.
- MeSH
- achondroplazie genetika patofyziologie MeSH
- buňky NIH 3T3 MeSH
- chondrocyty metabolismus MeSH
- chrupavka metabolismus MeSH
- cilie patologie fyziologie MeSH
- ciliopatie genetika patofyziologie MeSH
- fenotyp MeSH
- fibroblastové růstové faktory metabolismus MeSH
- lidé MeSH
- myši MeSH
- primární buněčná kultura MeSH
- receptor fibroblastových růstových faktorů, typ 3 genetika metabolismus MeSH
- růstová ploténka metabolismus MeSH
- signální transdukce fyziologie MeSH
- thanatoforní dysplazie genetika patofyziologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- FGFR3 protein, human MeSH Prohlížeč
- fibroblastové růstové faktory MeSH
- receptor fibroblastových růstových faktorů, typ 3 MeSH