Intestinal Na-P(i) cotransporter adaptation to dietary P(i) content in vitamin D receptor null mice

Am J Physiol Renal Physiol. 2004 Jul;287(1):F39-47. doi: 10.1152/ajprenal.00375.2003. Epub 2004 Mar 2.

Abstract

Recent studies suggest that vitamin D may play a role in intestinal Na(+)-dependent phosphate transport adaptation to variable levels of dietary P(i). Therefore, the goal of the current study was to assess Na(+)-dependent P(i) cotransport activity in transgenic mice to determine whether vitamin D is an essential mediator of this process. Intestinal brush-border membrane (BBM), Na(+)-dependent P(i) cotransport activity was significantly decreased in vitamin D receptor (VDR) null [VDR (-/-)] mice compared with wild-type (VDR+/+) mice. While intestinal Na-P(i) cotransporter (type IIb) mRNA levels were similar in VDR (-/-) and VDR (+/+) mice, type IIb Na-P(i) cotransporter protein expression was markedly suppressed in VDR (-/-) mice compared with VDR (+/+) mice. Furthermore, Na-P(i) cotransport activity in renal BBM was similar in VDR (-/-) and VDR (+/+) mice, but type IIa Na-P(i) cotransporter protein expression was decreased in VDR (-/-) mice. After administration of a low-P(i) diet, type IIb protein expression was significantly increased in VDR (+/+) and VDR (-/-) mice, and type IIb protein expression was present in the intestinal BBM of VDR (-/-) mice. These data demonstrate that intestinal Na-P(i) cotransport adaptation to a low-P(i) diet occurs independently of vitamin D.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diet
  • Gene Expression Regulation
  • Genotype
  • Immunohistochemistry
  • Mice
  • Mice, Knockout
  • Microvilli / physiology
  • Phosphates / deficiency*
  • Phosphates / metabolism*
  • Phosphorus, Dietary / metabolism*
  • Polymerase Chain Reaction
  • Receptors, Calcitriol / genetics*
  • Receptors, Calcitriol / physiology*
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Phosphate Cotransporter Proteins, Type IIa
  • Sodium-Phosphate Cotransporter Proteins, Type IIb
  • Symporters / physiology*
  • Vitamin D / genetics
  • Vitamin D / metabolism*

Substances

  • Phosphates
  • Phosphorus, Dietary
  • Receptors, Calcitriol
  • Slc34a1 protein, mouse
  • Slc34a2 protein, mouse
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Phosphate Cotransporter Proteins, Type IIa
  • Sodium-Phosphate Cotransporter Proteins, Type IIb
  • Symporters
  • Vitamin D