Literature DB >> 2893294

An H+-ATPase in opposite plasma membrane domains in kidney epithelial cell subpopulations.

D Brown1, S Hirsch, S Gluck.   

Abstract

Vectorial solute transport by epithelia requires the polarized insertion of transport proteins into apical or basolateral plasmalemmal domains. In the specialized intercalated cells of the kidney collecting duct, the selective placement of an apical plasma membrane proton-pumping ATPase (H+-ATPase) and of a basolateral membrane anion-exchange protein results in transepithelial proton secretion. It is currently believed that amino-acid sequences of membrane proteins contain critical signalling regions involved in sorting these proteins to specific membrane domains. Recently, it was proposed that intercalated cells can reverse their direction of proton secretion under different acid-base conditions by redirecting proton pumps from apical to basolateral membranes, and anion exchangers from basolateral to apical membranes. But others have found that antibodies raised against the red cell anion-exchange protein (Band 3) only labelled intercalated cells at the basolateral plasma membrane, providing evidence against the model of polarity reversal. In this report, we have examined directly the distribution of proton pumps in kidney intercalated cells using specific polyclonal antibodies against subunits of a bovine kidney medullary H+-ATPase. We find that some cortical collecting duct intercalated cells have apical plasma membrane proton pumps, whereas others have basolateral pumps. This is the first direct demonstration of neighbouring epithelial cells maintaining opposite polarities of a transport protein. Thus, either subtle structural differences exist between proton pumps located at opposite poles of the cell, or factors other than protein sequence determine the polarity of H+-ATPase insertion.

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Year:  1988        PMID: 2893294     DOI: 10.1038/331622a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  65 in total

1.  Acid incubation reverses the polarity of intercalated cell transporters, an effect mediated by hensin.

Authors:  George J Schwartz; Shuichi Tsuruoka; Soundarapandian Vijayakumar; Snezana Petrovic; Ayesa Mian; Qais Al-Awqati
Journal:  J Clin Invest       Date:  2002-01       Impact factor: 14.808

2.  Vacuolar-type H+ -ATPase distribution in unstimulated and acetylcholine-activated isolated human eccrine sweat glands.

Authors:  D L Bovell; M T Clunes; E Roussa; J Burry; H Y Elder
Journal:  Histochem J       Date:  2000-07

3.  Structural proton diffusion along lipid bilayers.

Authors:  Steffen Serowy; Sapar M Saparov; Yuri N Antonenko; Wladas Kozlovsky; Volker Hagen; Peter Pohl
Journal:  Biophys J       Date:  2003-02       Impact factor: 4.033

Review 4.  The structure and biochemistry of the vacuolar H+ ATPase in proximal and distal urinary acidification.

Authors:  S L Gluck
Journal:  J Bioenerg Biomembr       Date:  1992-08       Impact factor: 2.945

5.  Electrophysiological identification of alpha- and beta-intercalated cells and their distribution along the rabbit distal nephron segments.

Authors:  S Muto; K Yasoshima; K Yoshitomi; M Imai; Y Asano
Journal:  J Clin Invest       Date:  1990-12       Impact factor: 14.808

6.  Aldosterone stimulates vacuolar H(+)-ATPase activity in renal acid-secretory intercalated cells mainly via a protein kinase C-dependent pathway.

Authors:  Christian Winter; Nicole B Kampik; Luca Vedovelli; Florina Rothenberger; Teodor G Paunescu; Paul A Stehberger; Dennis Brown; Hubert John; Carsten A Wagner
Journal:  Am J Physiol Cell Physiol       Date:  2011-08-10       Impact factor: 4.249

Review 7.  Intracellular traffic of newly synthesized proteins. Current understanding and future prospects.

Authors:  V R Lingappa
Journal:  J Clin Invest       Date:  1989-03       Impact factor: 14.808

8.  Subtypes of intercalated cells in rat kidney collecting duct defined by antibodies against erythroid band 3 and renal vacuolar H+-ATPase.

Authors:  S L Alper; J Natale; S Gluck; H F Lodish; D Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

9.  The forkhead transcription factor Foxi1 directly activates the AE4 promoter.

Authors:  Ingo Kurth; Moritz Hentschke; Suna Hentschke; Uwe Borgmeyer; Andreas Gal; Christian A Hübner
Journal:  Biochem J       Date:  2006-01-01       Impact factor: 3.857

10.  Regulated Cl transport, K and Cl permeability, and exocytosis in T84 cells.

Authors:  M E Huflejt; R A Blum; S G Miller; H P Moore; T E Machen
Journal:  J Clin Invest       Date:  1994-05       Impact factor: 14.808

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