KRZYSCIK, Mateusz A, Kelly KARL, Pooja DUDEJA, Pavel KREJČÍ and Kalina HRISTOVA. Quantitative and qualitative differences in the activation of a fibroblast growth factor receptor by different FGF ligands. CYTOKINE & GROWTH FACTOR REVIEWS. London: ELSEVIER SCI LTD, 2024, vol. 78, August 2024, p. 77-84. ISSN 1359-6101. Available from: https://dx.doi.org/10.1016/j.cytogfr.2024.07.002.
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Basic information
Original name Quantitative and qualitative differences in the activation of a fibroblast growth factor receptor by different FGF ligands
Authors KRZYSCIK, Mateusz A, Kelly KARL, Pooja DUDEJA (356 India, belonging to the institution), Pavel KREJČÍ (203 Czech Republic, belonging to the institution) and Kalina HRISTOVA.
Edition CYTOKINE & GROWTH FACTOR REVIEWS, London, ELSEVIER SCI LTD, 2024, 1359-6101.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10601 Cell biology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 13.000 in 2022
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1016/j.cytogfr.2024.07.002
UT WoS 001297450100001
Keywords in English FGF; FGFR; Signaling; Bias
Tags 14110513, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 9/9/2024 08:36.
Abstract
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.
Links
GF21-26400K, research and development projectName: Vztah struktury a funkce v signálováni fibroblastových růstových faktorů
Investor: Czech Science Foundation, Lead Agency
LX22NPO5102, research and development projectName: Národní ústav pro výzkum rakoviny (Acronym: NÚVR)
Investor: Ministry of Education, Youth and Sports of the CR, National institute for cancer research, 5.1 EXCELES
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