Fibroblast growth factor 2 protein stability provides decreased dependence on heparin for induction of FGFR signaling and alters ERK signaling dynamics
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F27676013%3A_____%2F19%3AN0000004" target="_blank" >RIV/27676013:_____/19:N0000004 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14110/19:00108169 RIV/00159816:_____/19:00072535
Result on the web
<a href="https://www.frontiersin.org/articles/10.3389/fcell.2019.00331/full" target="_blank" >https://www.frontiersin.org/articles/10.3389/fcell.2019.00331/full</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3389/fcell.2019.00331" target="_blank" >10.3389/fcell.2019.00331</a>
Alternative languages
Result language
angličtina
Original language name
Fibroblast growth factor 2 protein stability provides decreased dependence on heparin for induction of FGFR signaling and alters ERK signaling dynamics
Original language description
In this study, the relationship between FGF2 stability, heparin dependence and ERK signaling dynamics using FGF2 variants with increased thermal stability (FGF2-STABs) was investigated. FGF2-STABs showed higher efficiency in induction of FGFR-mediated proliferation, lower affinity to heparin and were less dependent on heparin than wild-type FGF2 (FGF2-wt) for induction of FGFR-mediated mitogenic response. Interestingly, in primary mammary fibroblasts, FGF2-wt displayed a sigmoidal dose-response profile, while FGF2-STABs showed a biphasic response. Moreover, at low concentrations, FGF2-STABs induced ERK signaling more potently and displayed a faster dynamics of full ERK activation and higher amplitudes of ERK signaling than FGF2-wt. Our results suggest that FGF2 stability and heparin dependence are important factors in FGF-FGFR signaling complex assembly and ERK signaling dynamics.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10608 - Biochemistry and molecular biology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Frontiers in Cell and Developmental Biology
ISSN
2296-634X
e-ISSN
2296-634X
Volume of the periodical
7
Issue of the periodical within the volume
December 2019
Country of publishing house
GB - UNITED KINGDOM
Number of pages
15
Pages from-to
doi: 10.3389/fcell.2019.00331
UT code for WoS article
000514125200001
EID of the result in the Scopus database
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