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Mech Ageing Dev. 2010 Apr;131(4):270-5. doi: 10.1016/j.mad.2010.02.008. Epub 2010 Mar 1.

A potential link between phosphate and aging--lessons from Klotho-deficient mice.

Author information

1
Department of Pathology, The University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, TX 75390-9072, USA. Makoto.Kuro-o@UTSouthwestern.edu

Abstract

Phosphate homeostasis is maintained primarily by a bone-kidney endocrine axis. When phosphate is in excess, fibroblast growth factor-23 (FGF23) is secreted from bone and acts on kidney to promote phosphate excretion into urine. FGF23 also reduces serum vitamin D levels to suppress phosphate absorption from intestine. Thus, FGF23 functions as a hormone that induces negative phosphate balance. One critical feature of FGF23 is that it requires Klotho, a single-pass transmembrane protein expressed in renal tubules, as an obligate co-receptor to bind and activate cognate FGF receptors. Importantly, defects in either FGF23 or Klotho not only cause phosphate retention but also a premature-aging syndrome in mice, which can be rescued by resolving hyperphosphatemia. In addition, changes in extracellular and intracellular phosphate concentration affect glucose metabolism, insulin sensitivity, and oxidative stress in vivo and in vitro, which potentially affect aging processes. These findings suggest an unexpected link between inorganic phosphate and aging in mammals.

PMID:
20197072
PMCID:
PMC2862786
DOI:
10.1016/j.mad.2010.02.008
[Indexed for MEDLINE]
Free PMC Article

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