FGFR2 residence in primary cilia is necessary for epithelial cell signaling

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Publikace nespadá pod Ústav výpočetní techniky, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.
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NITĂ Alexandru POOVAKULATHU ABRAHAM Sara ELREFAAY Eman FAFÍLEK Bohumil ČÍŽKOVÁ Eliška URSACHI Vlad-Constantin GUDERNOVÁ Iva KOUDELKA Adolf DUDEJA Pooja GREGOR Tomáš FEKETOVÁ Zuzana RICO LLANOS Gustavo Adolfo SVOZILOVÁ Kateřina ÇELIKER Canan CZYREK Aleksandra Anna BÁRTA Tomáš TRANTÍREK Lukáš WIEDLOCHA Antoni KREJČÍ Pavel BOSÁKOVÁ Michaela

Rok publikování 2025
Druh Článek v odborném periodiku
Časopis / Zdroj Journal of cell biology
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://rupress.org/jcb/article/224/7/e202311030/277401/FGFR2-residence-in-primary-cilia-is-necessary-for
Klíčová slova Cilia; Development
Přiložené soubory
Popis Primary cilium projects from cells to provide a communication platform with neighboring cells and the surrounding environment. This is ensured by the selective entry of membrane receptors and signaling molecules, producing fine-tuned and effective responses to the extracellular cues. In this study, we focused on one family of signaling molecules, the fibroblast growth factor receptors (FGFRs), their residence within cilia, and its role in FGFR signaling. We show that FGFR1 and FGFR2, but not FGFR3 and FGFR4, localize to primary cilia of the developing mouse tissues and in vitro cells. For FGFR2, we demonstrate that the ciliary residence is necessary for its signaling and expression of target morphogenic genes. We also show that the pathogenic FGFR2 variants have minimal cilium presence, which can be rescued for the p.P253R variant associated with the Apert syndrome by using the RLY-4008 kinase inhibitor. Finally, we determine the molecular regulators of FGFR2 trafficking to cilia, including IFT144, BBS1, and the conserved T429V430 motif within FGFR2.
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