OpenSSL SSL_connect: Connection reset by peer in connection to v2.sherpa.ac.uk:443 PuSH - Publication Server of Helmholtz Zentrum München: PHEX, FGF23, DMP1 and beyond.

PuSH - Publication Server of Helmholtz Zentrum München

Strom, T.M. ; Jüppner, H.*

PHEX, FGF23, DMP1 and beyond.

Curr. Opin. Nephrol. Hypertens. 17, 357-362 (2008)
Open Access Green as soon as Postprint is submitted to ZB.
Purpose of review: We aim to review the biological properties of novel molecules that are members of a kidney-bone axis involved in the regulation of phosphate homeostasis. In addition, we describe how an improved knowledge of the mechanisms leading to changes in renal phosphate handling may lead to the development of novel therapeutic approaches. Recent findings: As yet, eight genes involved in the regulation of phosphate homeostasis have been identified through genetic studies. A key protein in this regulatory pathway is FGF23, which is made by osteocytes and activates renal KLOTHO/FGFR1 receptor heterodimers to inhibit renal phosphate reabsorption and 1,25-dihydroxyvitamin D synthesis. Gain-of-function mutations in FGF23, which render the hormone resistant to proteolytic cleavage, lead to increased phosphaturic activity. Furthermore, inactivating mutations in DMP1 and PHEX increase, through yet unknown mechanisms, FGF23 synthesis and thus enhance renal phosphate excretion. In contrast, loss-of-function mutations in FGF23 and KLOTHO, and abnormal O-glycosylation of FGF23 because of GALNT3 mutations, lead to diminished phosphate excretion. Extremely high levels of FGF23 are observed in chronic renal failure, which may contribute to the development of renal osteodystrophy. The analysis of rare genetic disorders affecting phosphate homeostasis led to the identification of several proteins that are essential for the renal regulation of phosphate homeostasis, although it is not yet completely understood how these proteins interact, and additional proteins are likely to contribute to these regulatory events.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords dentin matrix protein 1; fibroblast growth factor 23; PHEX; phosphate homeostasis
ISSN (print) / ISBN 1062-4821
e-ISSN 1473-6554
Journal Current Opinion in Nephrology & Hypertension
Quellenangaben Volume: 17, Issue: 4, Pages: 357-362 Article Number: , Supplement: ,
Publisher Lippincott Williams & Wilkins
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute of Human Genetics (IHG)