Literature DB >> 3005286

Polarized distribution of the Na+/H+ exchange system in a renal cell line (LLC-PK1) with characteristics of proximal tubular cells.

H F Cantiello, J A Scott, C A Rabito.   

Abstract

Studies of Na+ and H+ transport by confluent monolayers of the epithelial cell line LLC-PK1 were performed to verify the presence of a Na+/H+ exchange system. The presence of an outwardly directed H+ gradient produced a large stimulation of Na+ influx measured under net flux conditions. Amiloride (10(-3) M) completely inhibited Na+ influx stimulated by the H+ gradient and part of the Na+ influx measured in the absence of a pH gradient. Half-maximal inhibition of the Na+ influx stimulated by a pH gradient at 143 mM Na was observed at 5 microM amiloride. The presence of an inwardly oriented proton gradient also stimulated Na+ efflux from Na+-loaded cells. The stimulation was completely inhibited by the presence of 10(-3) M amiloride in the washout medium. These results indicate that this system could operate in the opposite direction depending on the orientation of the Na+ and H+ gradient. Incubation in Na+-free medium or in the presence of 10(-3) M ouabain resulted in a dramatic decrease of H+ release from LLC-PK1 cells. This H+ release was largely, although not completely, inhibited by 10(-4) M amiloride. Neither chloride substitution by the impermeable anion isethionate nor incubation in the presence of the ionophore valinomycin in high K+ medium affected Na+ influx by stimulated by a pH gradient. Inhibition of the Na+ influx by amiloride occurred only from the apical side of the monolayer. These results indicate that the Na+/H+ exchange system in LLC-PK1 monolayers is specifically localized in the apical membrane of the epithelial cells.

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Year:  1986        PMID: 3005286

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  10 in total

1.  Polarized expression of Na+/H+ exchange activities in clonal LLC-PK1 cells (Clone4 and PKE20) I. Basic characterization.

Authors:  V Casavola; C Helmle-Kolb; M H Montrose; H Murer
Journal:  Pflugers Arch       Date:  1991-04       Impact factor: 3.657

2.  Measurements of intracellular pH in single LLC-PK1 cells: recovery from an acid load via basolateral Na+/H+ exchange.

Authors:  M H Montrose; T Friedrich; H Murer
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

3.  Pharmacologically different Na/H antiporters on the apical and basolateral surfaces of cultured porcine kidney cells (LLC-PK1).

Authors:  J G Haggerty; N Agarwal; R F Reilly; E A Adelberg; C W Slayman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

4.  Regulation of pH in rat papillary tubule cells in primary culture.

Authors:  J G Kleinman; S S Blumenthal; J H Wiessner; K L Reetz; D L Lewand; N S Mandel; G S Mandel; J C Garancis; E J Cragoe
Journal:  J Clin Invest       Date:  1987-12       Impact factor: 14.808

5.  Polarized nature of taurine transport in LLC-PK1 and MDCK cells: Further characterization of divergent transport models.

Authors:  D P Jones; R W Chesney
Journal:  Amino Acids       Date:  1993-10       Impact factor: 3.520

6.  Oxalate transport in cultured porcine renal epithelial cells.

Authors:  T R Wandzilak; L Calo; S D'Andre; A Borsatti; H E Williams
Journal:  Urol Res       Date:  1992

7.  Toxicity of ifosfamide, cyclophosphamide and their metabolites in renal tubular cells in culture.

Authors:  M Mohrmann; S Ansorge; U Schmich; B Schönfeld; M Brandis
Journal:  Pediatr Nephrol       Date:  1994-04       Impact factor: 3.714

8.  Flow cytometric analysis of intracellular pH in cultured opossum kidney (OK) cells.

Authors:  M H Montrose; M A Condrau; H Murer
Journal:  J Membr Biol       Date:  1989-04       Impact factor: 1.843

9.  Effect of second messenger systems on oxalate uptake in renal epithelial cells.

Authors:  L Calò; T R Wandzilak; P A Davis; A Borsatti; H E Williams
Journal:  Urol Res       Date:  1995

10.  The application of renal cells in culture in studying drug-induced nephrotoxicity.

Authors:  P D Williams
Journal:  In Vitro Cell Dev Biol       Date:  1989-09
  10 in total

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