| Literature DB >> 26437603 |
Alexander Grabner1, Ansel P Amaral2, Karla Schramm2, Saurav Singh2, Alexis Sloan2, Christopher Yanucil2, Jihe Li3, Lina A Shehadeh4, Joshua M Hare3, Valentin David5, Aline Martin5, Alessia Fornoni1, Giovana Seno Di Marco6, Dominik Kentrup6, Stefan Reuter6, Anna B Mayer6, Hermann Pavenstädt6, Jörg Stypmann7, Christian Kuhn8, Susanne Hille8, Norbert Frey8, Maren Leifheit-Nestler9, Beatrice Richter9, Dieter Haffner9, Reimar Abraham10, Johannes Bange10, Bianca Sperl11, Axel Ullrich11, Marcus Brand6, Myles Wolf12, Christian Faul13.
Abstract
Chronic kidney disease (CKD) is a worldwide public health threat that increases risk of death due to cardiovascular complications, including left ventricular hypertrophy (LVH). Novel therapeutic targets are needed to design treatments to alleviate the cardiovascular burden of CKD. Previously, we demonstrated that circulating concentrations of fibroblast growth factor (FGF) 23 rise progressively in CKD and induce LVH through an unknown FGF receptor (FGFR)-dependent mechanism. Here, we report that FGF23 exclusively activates FGFR4 on cardiac myocytes to stimulate phospholipase Cγ/calcineurin/nuclear factor of activated T cell signaling. A specific FGFR4-blocking antibody inhibits FGF23-induced hypertrophy of isolated cardiac myocytes and attenuates LVH in rats with CKD. Mice lacking FGFR4 do not develop LVH in response to elevated FGF23, whereas knockin mice carrying an FGFR4 gain-of-function mutation spontaneously develop LVH. Thus, FGF23 promotes LVH by activating FGFR4, thereby establishing FGFR4 as a pharmacological target for reducing cardiovascular risk in CKD.Entities:
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Year: 2015 PMID: 26437603 PMCID: PMC4670583 DOI: 10.1016/j.cmet.2015.09.002
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287