[Vitamin D and phosphate metabolism; relationship with aging-regulating gene]

Clin Calcium. 2006 Jul;16(7):1137-42.
[Article in Japanese]

Abstract

It has been known that phosphate homeostasis is mainly regulated by parathyroid hormone and vitamin D. Fibroblast growth factor 23 (FGF23) has been identified as a novel factor that regulates vitamin D and phosphate metabolism. Genetic defect of FGF23 in mice revealed not only abnormal vitamin D and phosphate metabolism, but also premature aging-like phenotype that is quite similar to Klotho mice. Regulation of vitamin D and phosphate metabolism is closely related to aging processes as well as bone and mineral metabolism.

Publication types

  • Review

MeSH terms

  • Aging / genetics*
  • Aging, Premature / genetics
  • Animals
  • Bone and Bones / metabolism*
  • Fibroblast Growth Factor-23
  • Fibroblast Growth Factors / physiology*
  • Forkhead Transcription Factors
  • Glucuronidase / genetics
  • Humans
  • Insulin-Like Growth Factor I / physiology
  • Klotho Proteins
  • Mice
  • Phosphates / metabolism*
  • Phosphorus, Dietary / administration & dosage
  • Signal Transduction / genetics
  • Signal Transduction / physiology
  • Vitamin D / adverse effects
  • Vitamin D / metabolism
  • Vitamin D / physiology*

Substances

  • FGF23 protein, human
  • Fgf23 protein, mouse
  • Forkhead Transcription Factors
  • Phosphates
  • Phosphorus, Dietary
  • Vitamin D
  • Fibroblast Growth Factors
  • Insulin-Like Growth Factor I
  • Fibroblast Growth Factor-23
  • Glucuronidase
  • Klotho Proteins