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

Am J Physiol Cell Physiol. 2007 Feb;292(2):C927-34. doi: 10.1152/ajpcell.00126.2006. Epub 2006 Sep 20.

Abstract

Phosphate reabsorption in the renal proximal tubule occurs mostly via the type IIa Na(+)-phosphate cotransporter (NaP(i)-IIa) in the brush border membrane (BBM). The activity and localization of NaP(i)-IIa are regulated, among other factors, by parathyroid hormone (PTH). NaP(i)-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 NaP(i)-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 NaP(i)-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 NaP(i)-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 NaP(i)-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 NaP(i)-IIa and, specifically, couples the apical PTHR to PLC.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 8-Bromo Cyclic Adenosine Monophosphate / pharmacology
  • Animals
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Diglycerides / pharmacology
  • Endocytosis
  • Female
  • In Vitro Techniques
  • Ion Transport
  • Kidney Tubules, Proximal / metabolism*
  • Male
  • Mice
  • Mice, Knockout
  • Microvilli / metabolism
  • Parathyroid Hormone / pharmacology
  • Peptide Fragments / pharmacology
  • Phosphates / metabolism
  • Phosphoproteins / genetics
  • Phosphoproteins / physiology*
  • Protein Binding
  • Protein Kinase C / metabolism
  • Receptor, Parathyroid Hormone, Type 1 / agonists
  • Receptor, Parathyroid Hormone, Type 1 / metabolism*
  • Sodium-Hydrogen Exchangers / genetics
  • Sodium-Hydrogen Exchangers / physiology*
  • Sodium-Phosphate Cotransporter Proteins, Type IIa / metabolism*
  • Teriparatide / analogs & derivatives
  • Teriparatide / pharmacology
  • Type C Phospholipases / metabolism*

Substances

  • Diglycerides
  • Parathyroid Hormone
  • Peptide Fragments
  • Phosphates
  • Phosphoproteins
  • Receptor, Parathyroid Hormone, Type 1
  • Slc34a1 protein, mouse
  • Sodium-Hydrogen Exchangers
  • Sodium-Phosphate Cotransporter Proteins, Type IIa
  • sodium-hydrogen exchanger regulatory factor
  • 1,2-dioctanoylglycerol
  • parathyroid hormone (3-34)amide
  • Teriparatide
  • 8-Bromo Cyclic Adenosine Monophosphate
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C
  • Type C Phospholipases
  • parathyroid hormone (1-34)amide