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Effects of Npt2 gene ablation and low-phosphate diet on renal Na+/phosphate cotransport and cotransporter gene expression
Hannah M. Hoag, Josée Martel, Claude Gauthier, Harriet S. Tenenhouse
Hannah M. Hoag, Josée Martel, Claude Gauthier, Harriet S. Tenenhouse
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Article

Effects of Npt2 gene ablation and low-phosphate diet on renal Na+/phosphate cotransport and cotransporter gene expression

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Abstract

The renal Na+/phosphate (Pi) cotransporter Npt2 is expressed in the brush border membrane (BBM) of proximal tubular cells. We examined the effect of Npt2 gene knockout on age-dependent BBM Na+/Pi cotransport, expression of Na+/Pi cotransporter genes Npt1, Glvr-1, and Ram-1, and the adaptive response to chronic Pi deprivation. Na+/Pi cotransport declines with age in wild-type mice (Npt2+/+), but not in mice homozygous for the disrupted Npt2 allele (Npt2–/–). At all ages, Na+/Pi cotransport in Npt2–/– mice is approximately 15% of that in Npt2+/+ littermates. Only Npt1 mRNA abundance increases with age in Npt2+/+ mice, whereas Npt1, Glvr-1, and Ram-1 mRNAs show an age-dependent increase in Npt2–/– mice. Pi deprivation significantly increases Na+/Pi cotransport, Npt2 protein, and mRNA in Npt2+/+ mice. In contrast, Pi-deprived Npt2–/– mice fail to show the adaptive increase in transport despite exhibiting a fall in serum Pi. We conclude that (a) Npt2 is a major determinant of BBM Na+/Pi cotransport; (b) the age-dependent increase in Npt1, Glvr-1, and Ram-1 mRNAs in Npt2–/– mice is insufficient to compensate for loss of Npt2; and (c) Npt2 is essential for the adaptive BBM Na+/Pi cotransport response to Pi deprivation.

Authors

Hannah M. Hoag, Josée Martel, Claude Gauthier, Harriet S. Tenenhouse

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Figure 4

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Effect of Npt2 gene knockout and age on renal abundance of Npt1 (a), Glv...
Effect of Npt2 gene knockout and age on renal abundance of Npt1 (a), Glvr-1 (b), and Ram-1 (c) mRNAs. The abundance of each transcript, relative to β-actin mRNA, was determined in renal RNA samples derived from 21-, 45-, and 115-day-old Npt2+/+ (filled bars) and Npt2–/– (open bars) mice by ribonuclease protection assay as described in Methods. The values depict the mean ± SEM derived from 5–8 mice per group. *Effect of genotype, P < 0.05. §Effect of age, P < 0.05.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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