Hyperphosphatemia increases inflammation to exacerbate anemia and skeletal muscle wasting independently of FGF23-FGFR4 signaling.
FGF23
anemia
cell biology
chronic kidney disease
hepcidin
hyperphosphatemia
immunology
inflammation
mouse
Journal
eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614
Informations de publication
Date de publication:
18 03 2022
18 03 2022
Historique:
received:
17
10
2021
accepted:
17
03
2022
pubmed:
19
3
2022
medline:
5
4
2022
entrez:
18
3
2022
Statut:
epublish
Résumé
Elevations in plasma phosphate concentrations (hyperphosphatemia) occur in chronic kidney disease (CKD), in certain genetic disorders, and following the intake of a phosphate-rich diet. Whether hyperphosphatemia and/or associated changes in metabolic regulators, including elevations of fibroblast growth factor 23 (FGF23) directly contribute to specific complications of CKD is uncertain. Here, we report that similar to patients with CKD, mice with adenine-induced CKD develop inflammation, anemia, and skeletal muscle wasting. These complications are also observed in mice fed high phosphate diet even without CKD. Ablation of pathologic FGF23-FGFR4 signaling did not protect mice on an increased phosphate diet or mice with adenine-induced CKD from these sequelae. However, low phosphate diet ameliorated anemia and skeletal muscle wasting in a genetic mouse model of CKD. Our mechanistic in vitro studies indicate that phosphate elevations induce inflammatory signaling and increase hepcidin expression in hepatocytes, a potential causative link between hyperphosphatemia, anemia, and skeletal muscle dysfunction. Our study suggests that high phosphate intake, as caused by the consumption of processed food, may have harmful effects irrespective of pre-existing kidney injury, supporting not only the clinical utility of treating hyperphosphatemia in CKD patients but also arguing for limiting phosphate intake in healthy individuals.
Identifiants
pubmed: 35302487
doi: 10.7554/eLife.74782
pii: 74782
pmc: PMC8963881
doi:
pii:
Substances chimiques
Fgf23 protein, mouse
0
Fibroblast Growth Factors
62031-54-3
Fibroblast Growth Factor-23
7Q7P4S7RRE
FGFR4 protein, human
EC 2.7.10.1
Receptor, Fibroblast Growth Factor, Type 4
EC 2.7.10.1
Banques de données
Dryad
['10.5061/dryad.6t1g1jx0f']
Types de publication
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIDDK NIH HHS
ID : F31 DK127640
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK128068
Pays : United States
Organisme : NIDDK NIH HHS
ID : F31 DK117550
Pays : United States
Organisme : NIDDK NIH HHS
ID : K08 DK111980
Pays : United States
Organisme : NIDDK NIH HHS
ID : F31 DK115074
Pays : United States
Organisme : NIDDK NIH HHS
ID : F31 DK131914
Pays : United States
Organisme : NIDDK NIH HHS
ID : K24 DK116180
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL128714
Pays : United States
Organisme : NIDCR NIH HHS
ID : T90 DE022736
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK087727
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK125459
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL145528
Pays : United States
Informations de copyright
© 2022, Czaya et al.
Déclaration de conflit d'intérêts
BC, KH, IC, CY, DK, DW, GJ, IS, MH No competing interests declared, OG has received honoraria and grant support from Akebia and Amgen, grant support from GSK, honoraria from Ardelyx, Reata, and AstraZeneca, and serves on the Data Monitoring Committee for QED, JB has ownership interest in Ferrumax Pharmaceuticals and has been a consultant for Incyte Corporation, and Alnylam Pharmaceuticals, CF has served as a consultant for Bayer and Calico Labs, and he is the founder and currently the CSO of a startup biotech company (Alpha Young LLC)
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