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FHF1 is a bona fide fibroblast growth factor that activates cellular signaling in FGFR-dependent manner
ABSTRACT: Fibroblast growth factors (FGFs) via their receptors (FGFRs) transduce signals from the extracellular space to the cell interior, modulating pivotal cellular processes such as cell proliferation, motility, metabolism and death. FGF superfamily includes a group of fibroblast growth factor h...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193404/ https://www.ncbi.nlm.nih.gov/pubmed/32357892 http://dx.doi.org/10.1186/s12964-020-00573-2 |
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author | Sochacka, Martyna Opalinski, Lukasz Szymczyk, Jakub Zimoch, Marta B. Czyrek, Aleksandra Krowarsch, Daniel Otlewski, Jacek Zakrzewska, Malgorzata |
author_facet | Sochacka, Martyna Opalinski, Lukasz Szymczyk, Jakub Zimoch, Marta B. Czyrek, Aleksandra Krowarsch, Daniel Otlewski, Jacek Zakrzewska, Malgorzata |
author_sort | Sochacka, Martyna |
collection | PubMed |
description | ABSTRACT: Fibroblast growth factors (FGFs) via their receptors (FGFRs) transduce signals from the extracellular space to the cell interior, modulating pivotal cellular processes such as cell proliferation, motility, metabolism and death. FGF superfamily includes a group of fibroblast growth factor homologous factors (FHFs), proteins whose function is still largely unknown. Since FHFs lack the signal sequence for secretion and are unable to induce FGFR-dependent cell proliferation, these proteins were considered as intracellular proteins that are not involved in signal transduction via FGFRs. Here we demonstrate for the first time that FHF1 directly interacts with all four major FGFRs. FHF1 binding causes efficient FGFR activation and initiation of receptor-dependent signaling cascades. However, the biological effect of FHF1 differs from the one elicited by canonical FGFs, as extracellular FHF1 protects cells from apoptosis, but is unable to stimulate cell division. Our data define FHF1 as a FGFR ligand, emphasizing much greater similarity between FHFs and canonical FGFs than previously indicated. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-7193404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71934042020-05-06 FHF1 is a bona fide fibroblast growth factor that activates cellular signaling in FGFR-dependent manner Sochacka, Martyna Opalinski, Lukasz Szymczyk, Jakub Zimoch, Marta B. Czyrek, Aleksandra Krowarsch, Daniel Otlewski, Jacek Zakrzewska, Malgorzata Cell Commun Signal Short Report ABSTRACT: Fibroblast growth factors (FGFs) via their receptors (FGFRs) transduce signals from the extracellular space to the cell interior, modulating pivotal cellular processes such as cell proliferation, motility, metabolism and death. FGF superfamily includes a group of fibroblast growth factor homologous factors (FHFs), proteins whose function is still largely unknown. Since FHFs lack the signal sequence for secretion and are unable to induce FGFR-dependent cell proliferation, these proteins were considered as intracellular proteins that are not involved in signal transduction via FGFRs. Here we demonstrate for the first time that FHF1 directly interacts with all four major FGFRs. FHF1 binding causes efficient FGFR activation and initiation of receptor-dependent signaling cascades. However, the biological effect of FHF1 differs from the one elicited by canonical FGFs, as extracellular FHF1 protects cells from apoptosis, but is unable to stimulate cell division. Our data define FHF1 as a FGFR ligand, emphasizing much greater similarity between FHFs and canonical FGFs than previously indicated. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2020-05-01 /pmc/articles/PMC7193404/ /pubmed/32357892 http://dx.doi.org/10.1186/s12964-020-00573-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Short Report Sochacka, Martyna Opalinski, Lukasz Szymczyk, Jakub Zimoch, Marta B. Czyrek, Aleksandra Krowarsch, Daniel Otlewski, Jacek Zakrzewska, Malgorzata FHF1 is a bona fide fibroblast growth factor that activates cellular signaling in FGFR-dependent manner |
title | FHF1 is a bona fide fibroblast growth factor that activates cellular signaling in FGFR-dependent manner |
title_full | FHF1 is a bona fide fibroblast growth factor that activates cellular signaling in FGFR-dependent manner |
title_fullStr | FHF1 is a bona fide fibroblast growth factor that activates cellular signaling in FGFR-dependent manner |
title_full_unstemmed | FHF1 is a bona fide fibroblast growth factor that activates cellular signaling in FGFR-dependent manner |
title_short | FHF1 is a bona fide fibroblast growth factor that activates cellular signaling in FGFR-dependent manner |
title_sort | fhf1 is a bona fide fibroblast growth factor that activates cellular signaling in fgfr-dependent manner |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193404/ https://www.ncbi.nlm.nih.gov/pubmed/32357892 http://dx.doi.org/10.1186/s12964-020-00573-2 |
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