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Localization and interaction of NHERF isoforms in the renal proximal tubule of the mouse.

Publication ,  Journal Article
Wade, JB; Liu, J; Coleman, RA; Cunningham, R; Steplock, DA; Lee-Kwon, W; Pallone, TL; Shenolikar, S; Weinman, EJ
Published in: Am J Physiol Cell Physiol
December 2003

In expression systems and in yeast, Na/H exchanger regulatory factor (NHERF)-1 and NHERF-2 have been demonstrated to interact with the renal brush border membrane proteins NHE3 and Npt2. In renal tissue of mice, however, NHERF-1 is required for cAMP regulation of NHE3 and for the apical targeting of Npt2 despite the presence of NHERF-2, suggesting another order of specificity. The present studies examine the subcellular location of NHERF-1 and NHERF-2 and their interactions with target proteins including NHE3, Npt2, and ezrin. The wild-type mouse proximal tubule expresses both NHERF-1 and NHERF-2 in a distinct pattern. NHERF-1 is strongly expressed in microvilli in association with NHE3, Npt2, and ezrin. Although NHERF-2 can be detected weakly in the microvilli, it is expressed predominantly at the base of the microvilli in the vesicle-rich domain. NHERF-2 appears to associate directly with ezrin and NHE3 but not Npt2. NHERF-1 is involved in the apical expression of Npt2 and the presence of other Npt2-binding proteins does not compensate totally for the absence of NHERF-1 in NHERF-1-null mice. Although NHERF-1 links NHE3 to the actin cytoskeleton through ezrin, the absence of NHERF-1 does not result in a generalized disruption of the architecture of the cell. Thus the mistargeting of Npt2 seen in NHERF-1-null mice likely represents a specific disruption of pathways mediated by NHERF-1 to achieve targeting of Npt2. These findings suggest that the organized subcellular distribution of the NHERF isoforms may play a role in the specific interactions mediating physiological control of transporter function.

Duke Scholars

Published In

Am J Physiol Cell Physiol

DOI

ISSN

0363-6143

Publication Date

December 2003

Volume

285

Issue

6

Start / End Page

C1494 / C1503

Location

United States

Related Subject Headings

  • Symporters
  • Sodium-Phosphate Cotransporter Proteins, Type III
  • Sodium-Phosphate Cotransporter Proteins, Type I
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Hydrogen Exchangers
  • Sodium-Hydrogen Exchanger 3
  • Protein Isoforms
  • Precipitin Tests
  • Physiology
  • Phosphoproteins
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Wade, J. B., Liu, J., Coleman, R. A., Cunningham, R., Steplock, D. A., Lee-Kwon, W., … Weinman, E. J. (2003). Localization and interaction of NHERF isoforms in the renal proximal tubule of the mouse. Am J Physiol Cell Physiol, 285(6), C1494–C1503. https://doi.org/10.1152/ajpcell.00092.2003
Wade, James B., Jie Liu, Richard A. Coleman, Rochelle Cunningham, Deborah A. Steplock, Whaseon Lee-Kwon, Thomas L. Pallone, Shirish Shenolikar, and Edward J. Weinman. “Localization and interaction of NHERF isoforms in the renal proximal tubule of the mouse.Am J Physiol Cell Physiol 285, no. 6 (December 2003): C1494–1503. https://doi.org/10.1152/ajpcell.00092.2003.
Wade JB, Liu J, Coleman RA, Cunningham R, Steplock DA, Lee-Kwon W, et al. Localization and interaction of NHERF isoforms in the renal proximal tubule of the mouse. Am J Physiol Cell Physiol. 2003 Dec;285(6):C1494–503.
Wade, James B., et al. “Localization and interaction of NHERF isoforms in the renal proximal tubule of the mouse.Am J Physiol Cell Physiol, vol. 285, no. 6, Dec. 2003, pp. C1494–503. Pubmed, doi:10.1152/ajpcell.00092.2003.
Wade JB, Liu J, Coleman RA, Cunningham R, Steplock DA, Lee-Kwon W, Pallone TL, Shenolikar S, Weinman EJ. Localization and interaction of NHERF isoforms in the renal proximal tubule of the mouse. Am J Physiol Cell Physiol. 2003 Dec;285(6):C1494–C1503.

Published In

Am J Physiol Cell Physiol

DOI

ISSN

0363-6143

Publication Date

December 2003

Volume

285

Issue

6

Start / End Page

C1494 / C1503

Location

United States

Related Subject Headings

  • Symporters
  • Sodium-Phosphate Cotransporter Proteins, Type III
  • Sodium-Phosphate Cotransporter Proteins, Type I
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Hydrogen Exchangers
  • Sodium-Hydrogen Exchanger 3
  • Protein Isoforms
  • Precipitin Tests
  • Physiology
  • Phosphoproteins