Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities

Proc Natl Acad Sci U S A. 1998 Apr 28;95(9):5372-7. doi: 10.1073/pnas.95.9.5372.

Abstract

Npt2 encodes a renal-specific, brush-border membrane Na+-phosphate (Pi) cotransporter that is expressed in the proximal tubule where the bulk of filtered Pi is reabsorbed. Mice deficient in the Npt2 gene were generated by targeted mutagenesis to define the role of Npt2 in the overall maintenance of Pi homeostasis, determine its impact on skeletal development, and clarify its relationship to autosomal disorders of renal Pi reabsorption in humans. Homozygous mutants (Npt2(-/-)) exhibit increased urinary Pi excretion, hypophosphatemia, an appropriate elevation in the serum concentration of 1,25-dihydroxyvitamin D with attendant hypercalcemia, hypercalciuria and decreased serum parathyroid hormone levels, and increased serum alkaline phosphatase activity. These biochemical features are typical of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH), a Mendelian disorder of renal Pi reabsorption. However, unlike HHRH patients, Npt2(-/-) mice do not have rickets or osteomalacia. At weaning, Npt2(-/-) mice have poorly developed trabecular bone and retarded secondary ossification, but, with increasing age, there is a dramatic reversal and eventual overcompensation of the skeletal phenotype. Our findings demonstrate that Npt2 is a major regulator of Pi homeostasis and necessary for normal skeletal development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport
  • Body Weight
  • Bone and Bones / abnormalities*
  • Bone and Bones / pathology
  • Calcitriol / metabolism
  • Calcium / urine
  • Carrier Proteins / physiology*
  • Female
  • Gene Expression
  • Heterozygote
  • Kidney / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Microvilli / metabolism
  • Phosphates / metabolism*
  • Phosphates / urine
  • RNA, Messenger / genetics
  • Sodium / metabolism*
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Phosphate Cotransporter Proteins, Type I
  • Sodium-Phosphate Cotransporter Proteins, Type III
  • Symporters*

Substances

  • Carrier Proteins
  • Phosphates
  • RNA, Messenger
  • Slc17a2 protein, mouse
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Phosphate Cotransporter Proteins, Type I
  • Sodium-Phosphate Cotransporter Proteins, Type III
  • Symporters
  • Sodium
  • Calcitriol
  • Calcium