Quantitative and qualitative differences in the activation of a fibroblast growth factor receptor by different FGF ligands
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985904%3A_____%2F24%3A00597897" target="_blank" >RIV/67985904:_____/24:00597897 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216224:14110/24:00137051 RIV/00159816:_____/24:00081491
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S1359610124000443?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1359610124000443?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.cytogfr.2024.07.002" target="_blank" >10.1016/j.cytogfr.2024.07.002</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Quantitative and qualitative differences in the activation of a fibroblast growth factor receptor by different FGF ligands
Popis výsledku v původním jazyce
The FGF system is the most complex of all receptor tyrosine kinase signaling networks with 18 FGF ligands and four FGFRs that deliver morphogenic signals to pattern most embryonic structures. Even when a single FGFR is expressed in the tissue, different FGFs can trigger dramatically different biological responses via this receptor. Here we show both quantitative and qualitative differences in the signaling of one of the FGF receptors, FGFR1c, in response to different FGFs. We provide an overview of the recent discovery that FGFs engage in biased signaling via FGFR1c. We discuss the concept of ligand bias, which represents qualitative differences in signaling as it is a measure of differential ligand preferences for different downstream responses. We show how FGF ligand bias manifests in functional data in cultured chondrocyte cells. We argue that FGF-ligand bias contributes substantially to FGF-driven developmental processes, along with known differences in FGF expression levels, FGF-FGFR binding coefficients and differences in FGF stability in vivo.
Název v anglickém jazyce
Quantitative and qualitative differences in the activation of a fibroblast growth factor receptor by different FGF ligands
Popis výsledku anglicky
The FGF system is the most complex of all receptor tyrosine kinase signaling networks with 18 FGF ligands and four FGFRs that deliver morphogenic signals to pattern most embryonic structures. Even when a single FGFR is expressed in the tissue, different FGFs can trigger dramatically different biological responses via this receptor. Here we show both quantitative and qualitative differences in the signaling of one of the FGF receptors, FGFR1c, in response to different FGFs. We provide an overview of the recent discovery that FGFs engage in biased signaling via FGFR1c. We discuss the concept of ligand bias, which represents qualitative differences in signaling as it is a measure of differential ligand preferences for different downstream responses. We show how FGF ligand bias manifests in functional data in cultured chondrocyte cells. We argue that FGF-ligand bias contributes substantially to FGF-driven developmental processes, along with known differences in FGF expression levels, FGF-FGFR binding coefficients and differences in FGF stability in vivo.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10605 - Developmental biology
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Cytokine & Growth Factor Reviews
ISSN
1359-6101
e-ISSN
1879-0305
Svazek periodika
78
Číslo periodika v rámci svazku
AUG 24
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
8
Strana od-do
77-84
Kód UT WoS článku
001297450100001
EID výsledku v databázi Scopus
2-s2.0-85199151120