Urine electrolyte, mineral, and protein excretion in NHERF-2 and NHERF-1 null mice

R Cunningham, A Esmaili, E Brown, RS Biswas, R Murtazina, M Donowitz, HB Dijkman, J van der Vlag, Boris Hogema, Hugo de Jonge, S Shenolikar, JB Wade, EJ Weinman

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Urine electrolyte, mineral, and protein excretion in NHERF- 2 and NHERF-1 null mice. Am J Physiol Renal Physiol 294: F1001-F1007, 2008. First published February 6, 2008; doi:10.1152/ajprenal.00504.2007. -The adaptor proteins sodium/hydrogen exchanger regulatory factor (NHERF)-1 and NHERF-2 have overlapping tissue distribution in renal cells and overlapping specificity in their binding to renal transporters and other proteins. To compare the kidney-specific differences in the function of these adaptor proteins, NHERF-1 and NHERF 2 null mice were compared with wild-type control mice. In NHERF-2 null mice, the renal proximal tubule abundance and distribution of NHERF-1 and NHERF-3 were not different from those in wild-type animals. The glomerular expression of podocalyxin and ZO-1 also did not differ. NHERF-1 null mice had increased urinary excretion of phosphate, calcium, and uric acid compared with wild-type control and NHERF-2 null mice. Because of the association between NHERF-2 and podocalyxin in glomeruli and ClC-5 in the renal proximal tubule, the urinary excretion of protein was determined. There were no differences in the urinary excretion of protein or low-molecular-weight proteins between wild-type control, NHERF-1(-/-), and NHERF-2(-/-) mice. These studies indicate that the increased urinary excretion of phosphate and uric acid are specific to NHERF-1 null mice and highlight the fact that predictions about the role of adaptor proteins such as the NHERF proteins obtained from studies of model cell systems must be confirmed in whole animals.
Original languageUndefined/Unknown
Pages (from-to)F1001-F1007
JournalAmerican Journal of Physiology-Renal Physiology
Issue number4
Publication statusPublished - 2008

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  • EMC MGC-02-21-02

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