|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symposium reports |
1 Institute of Physiology, Zurich University, CH-8057, Zurich, Switzerland
2 Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA
Regulation of renal proximal tubular reabsorption of phosphate (Pi) is one of the critical steps in Pi homeostasis. Experimental evidence suggests that this regulation is achieved mainly by controlling the apical expression of the Na+-dependent Pi cotransporter type IIa (NaPi-IIa) in proximal tubules. Only recently have we started to obtain information regarding the molecular mechanisms that control the apical expression of NaPi-IIa. The first critical observation was the finding that truncation of only its last three amino acid residues has a strong effect on apical expression. A second major finding was the observation that the last intracellular loop of NaPi-IIa contains sequence information that confers parathyroid hormone (PTH) sensitivity. The use of the above domains of the cotransporter in yeast two-hybrid (Y2H) screening allowed the identification of proteins interacting with NaPi-IIa. Biochemical and morphological, as well as functional, analyses have allowed us to obtain insights into the physiological roles of such interactions, although our present knowledge is still far from complete.
(Received 21 March 2005;
accepted after revision 9 May 2005;
first published online 12 May 2005)
Corresponding author N. Hernando: Physiologisches Institute, Universität Zürich-Irchel, Winterthurerstrasse 190; CH-8057 Zurich, Switzerland. Email: hernando{at}physiol.unizh.ch
This article has been cited by other articles:
![]() |
M. Levi and S. Bruesegem Renal Phosphate-Transporter Regulatory Proteins and Nephrolithiasis N. Engl. J. Med., September 11, 2008; 359(11): 1171 - 1173. [Full Text] [PDF] |
||||
![]() |
L. V. Virkki, J. Biber, H. Murer, and I. C. Forster Phosphate transporters: a tale of two solute carrier families Am J Physiol Renal Physiol, September 1, 2007; 293(3): F643 - F654. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Murtazina, O. Kovbasnjuk, N. C. Zachos, X. Li, Y. Chen, A. Hubbard, B. M. Hogema, D. Steplock, U. Seidler, K. M. Hoque, et al. Tissue-specific Regulation of Sodium/Proton Exchanger Isoform 3 Activity in Na+/H+ Exchanger Regulatory Factor 1 (NHERF1) Null Mice: cAMP INHIBITION IS DIFFERENTIALLY DEPENDENT ON NHERF1 AND EXCHANGE PROTEIN DIRECTLY ACTIVATED BY cAMP IN ILEUM VERSUS PROXIMAL TUBULE J. Biol. Chem., August 24, 2007; 282(34): 25141 - 25151. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Donowitz and X. Li Regulatory Binding Partners and Complexes of NHE3 Physiol Rev, July 1, 2007; 87(3): 825 - 872. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Lanaspa, H. Giral, S. Y. Breusegem, N. Halaihel, G. Baile, J. Catalan, J. A. Carrodeguas, N. P. Barry, M. Levi, and V. Sorribas Interaction of MAP17 with NHERF3/4 induces translocation of the renal Na/Pi IIa transporter to the trans-Golgi Am J Physiol Renal Physiol, January 1, 2007; 292(1): F230 - F242. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Donowitz, S. Milgram, H. Murer, Y. Kurachi, C. Yun, and E. Weinman Coming out of the NHERF family J. Physiol., August 15, 2005; 567(1): 1 - 1. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |