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Am J Physiol Cell Physiol 292: C927-C934, 2007. First published September 20, 2006; doi:10.1152/ajpcell.00126.2006
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RECEPTORS AND SIGNAL TRANSDUCTION

Defective coupling of apical PTH receptors to phospholipase C prevents internalization of the Na+-phosphate cotransporter NaPi-IIa in Nherf1-deficient mice

Paola Capuano,1,* Desa Bacic,1,2,* Marcel Roos,1 Serge M. Gisler,1 Gerti Stange,1 Jürg Biber,1 Brigitte Kaissling,2 Edward J. Weinman,3 Shirish Shenolikar,4 Carsten A. Wagner,1 and Heini Murer1

1Institute of Physiology and Center for Human Integrative Physiology and 2Institute of Anatomy, University of Zurich, Zurich, Switzerland; 3Division of Nephrology, University of Maryland School of Medicine and Department Veterans Affairs Medical Center, Baltimore, Maryland; and 4Duke University Medical Center, Durham, North Carolina

Submitted 21 March 2006 ; accepted in final form 17 September 2006

Phosphate reabsorption in the renal proximal tubule occurs mostly via the type IIa Na+-phosphate cotransporter (NaPi-IIa) in the brush border membrane (BBM). The activity and localization of NaPi-IIa are regulated, among other factors, by parathyroid hormone (PTH). NaPi-IIa interacts in vitro via its last three COOH-terminal amino acids with the PDZ protein Na+/H+-exchanger isoform 3 regulatory factor (NHERF)-1 (NHERF1). Renal phosphate reabsorption in Nherf1-deficient mice is altered, and NaPi-IIa expression in the BBM is reduced. In addition, it has been proposed that NHERF1 and NHERF2 are important for the coupling of PTH receptors (PTHRs) to phospholipase C (PLC) and the activation of the protein kinase C pathway. We tested the role of NHERF1 in the regulation of NaPi-IIa by PTH in Nherf1-deficient mice. Immunohistochemistry and Western blotting demonstrated that stimulation of apical and basolateral receptors with PTH-(1–34) led to internalization of NaPi-IIa in wild-type and Nherf1-deficient mice. Stimulation of only apical receptors with PTH-(3–34) failed to induce internalization in Nherf1-deficient mice. Expression and localization of apical PTHRs were similar in wild-type and Nherf1-deficient mice. Activation of the protein kinase C- and A-dependent pathways with 1,2-dioctanoyl-sn-glycerol or 8-bromo-cAMP induced normal internalization of NaPi-IIa in wild-type, as well as Nherf1-deficient, mice. Stimulation of PLC activity due to apical PTHRs was impaired in Nherf1-deficient mice. These data suggest that NHERF1 in the proximal tubule is important for PTH-induced internalization of NaPi-IIa and, specifically, couples the apical PTHR to PLC.

phosphate cotransporter; PDZ protein; parathyroid hormone; proximal tubule



Address for reprint requests and other correspondence: C. A. Wagner, Institute of Physiology, Univ. of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland (e-mail: Wagnerca{at}access.unizh.ch)




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