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Mice lacking the vitamin D receptor exhibit impaired bone formation, uterine hypoplasia and growth retardation after weaning.

1 alpha,25-Dihydroxyvitamin D3[1 alpha,25(OH)2D3], an active form of vitamin D, has roles in many biological phenomena such as calcium homeostasis and bone formation, which are thought to be mediated by the 1 alpha,25(OH)2D3 receptor (VDR), a member of the nuclear hormone receptor superfamily. However, the molecular basis for the actions of 1 alpha,25(OH)2D3 in bone formation, its role during development and VDR genetic polymorphisms for predicting bone mineral density are uncertain. To investigate the functional role of VDR, we generated mice deficient in VDR by gene targeting. We report here that in VDR null mutant mice, no defects in development and growth were observed before weaning, irrespective of reduced expression of vitamin D target genes. After weaning, however, mutants failed to thrive, with appearance of alopoecia, hypocalcaemia and infertility, and bone formation was severely impaired as a typical feature of vitamin D-dependent rickets type II (refs 8, 9). Unlike humans with this disease, most of the null mutant mice died within 15 weeks after birth, and uterine hypoplasia with impaired folliculogenesis was found in female reproductive organs. These defects, such as alopoecia and uterine hypoplasia, were not observed in vitamin D-deficient animals. The findings establish a critical role for VDR in growth, bone formation and female reproduction in the post-weaning stage.

Pubmed ID: 9241280

Authors

  • Yoshizawa T
  • Handa Y
  • Uematsu Y
  • Takeda S
  • Sekine K
  • Yoshihara Y
  • Kawakami T
  • Arioka K
  • Sato H
  • Uchiyama Y
  • Masushige S
  • Fukamizu A
  • Matsumoto T
  • Kato S

Journal

Nature genetics

Publication Data

August 28, 1997

Associated Grants

None

Mesh Terms

  • Alopecia
  • Animals
  • Body Weight
  • Bone Development
  • Calbindins
  • Cell Line
  • Durapatite
  • Female
  • Gene Deletion
  • Gene Expression
  • Growth Disorders
  • Humans
  • Male
  • Mice
  • Osteopontin
  • Receptors, Calcitriol
  • Rickets
  • S100 Calcium Binding Protein G
  • Sialoglycoproteins
  • Uterus
  • Weaning