Literature DB >> 6260815

Interaction of ouabain with the Na+ pump in intact epithelial cells.

J W Mills, A D Macknight, J A Jarrell, J M Dayer, D A Ausiello.   

Abstract

To determine the specificity and efficacy of [(3)H]ouabain binding as a quantitative measure of the Na(+) pump (Na(+), K(+)-ATPase) and as a marker for the localization of pumps involved in transepithelial Na(+)-transport, we analyzed the interaction of [(3)H]ouabain with its receptor in pig kidney epithelial (LLC-PK(1)) cells. When these epithelial cells are depleted of Na(+) and exposed to 2 muM [(3)H]ouabain in a Na(+)-free medium, binding is reduced by 90 percent. When depleted of K(+) and incubated in a K(+)- free medium, the ouabain binding rate is increase compared with that measured at 5 mM. This increase is only demonstable when Na(+) is present. The increased rate could be attributed to the predominance of the Na(+)-stimulated phosphorylated form of the pump, as K(+) is not readily available to stimulate dephosphorylation. However, some binding in the K(+)-free medium is attributable to pump turnover (and therefore, recycling of K(+)), because analysis of K(+)-washout kinetics demonstrated that addition of 2 muM ouabain to K(+)-depleted cells increased the rate of K(+) loss. These results indicate that in intact epithelial cells, unlike isolated membrane preparations, the most favorable condition for supporting ouabain binding occurs when the Na(+), K(+)-ATPase is operating in the Na(+)-pump mode or is phosphorylated in the presence of Na(+). When LLC-PK(1) cells were exposed to ouabain at 4 degrees C, binding was reduced by 97 percent. Upon rewarming, the rate of binding was greater than that obtained on cells kept at a constant 37 degrees C. However, even at this accelerated rate, the time to reach equilibrium was beyond what is required for cells, swollen by exposure to cold, to recover normal volume. Thus, results from studies that have attempted to use ouabain to eliminate the contribution of the conventional Na(+) pump to volume recovery must be reevaluated if the exposure to ouabain was done in the cold or under conditions in which the Na(+) pump is not operating.

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Year:  1981        PMID: 6260815      PMCID: PMC2112757          DOI: 10.1083/jcb.88.3.637

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  23 in total

1.  Mechanism of cardiac glycoside inhibition of the (Na+-K+)-dependent ATPase from cardiac tissue.

Authors:  H Matsui; A Schwartz
Journal:  Biochim Biophys Acta       Date:  1968-03-25

2.  Binding of the cardiac glycoside ouabain to intact cells.

Authors:  P F Baker; J S Willis
Journal:  J Physiol       Date:  1972-07       Impact factor: 5.182

3.  Adenosine triphosphatase and active cation transport in red blood cell membranes.

Authors:  P B Dunham; R B Gunn
Journal:  Arch Intern Med       Date:  1972-02

4.  The ouabain inhibition of sugar transport in kidney cortex cells.

Authors:  J A Almendares; A Kleinzeller
Journal:  Arch Biochem Biophys       Date:  1971-08       Impact factor: 4.013

5.  Water and electrolyte contents of rat renal cortical slices incubated in potassium-free media and media containing ouabain.

Authors:  A D Macknight
Journal:  Biochim Biophys Acta       Date:  1968-03-01

Review 6.  The red cell membrane and the transport of sodium and potassium.

Authors:  J F Hoffman
Journal:  Am J Med       Date:  1966-11       Impact factor: 4.965

7.  Two modes of Na extrusion in cells from guinea pig kidney cortex slices.

Authors:  G Whittembury; F Proverbio
Journal:  Pflugers Arch       Date:  1970       Impact factor: 3.657

8.  Sodium uptake by frog skin and its modification by inhibitors of transepithelial sodium transport.

Authors:  D Erlij; M W Smith
Journal:  J Physiol       Date:  1973-01       Impact factor: 5.182

9.  Ouabain binding to renal tubules of the rabbit.

Authors:  J L Shaver; C Stirling
Journal:  J Cell Biol       Date:  1978-02       Impact factor: 10.539

10.  Radioautographic localization of sodium pump sites in rabbit intestine.

Authors:  C E Stirling
Journal:  J Cell Biol       Date:  1972-06       Impact factor: 10.539

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  8 in total

1.  Glucagon stimulation of hepatic Na+, K+-ATPase.

Authors:  N Kraus-Friedmann; L Hummel; A Radominska-Pyrek; J M Little; R Lester
Journal:  Mol Cell Biochem       Date:  1982-05-14       Impact factor: 3.396

Review 2.  Cellular lithium and transepithelial transport across toad urinary bladder.

Authors:  P M Hughes; A D Macknight
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

3.  Electrophysiological study of transport systems in isolated perfused pancreatic ducts: properties of the basolateral membrane.

Authors:  I Novak; R Greger
Journal:  Pflugers Arch       Date:  1988-01       Impact factor: 3.657

4.  H+-gradient-dependent active transport of tetraethylammonium cation in apical-membrane vesicles isolated from kidney epithelial cell line LLC-PK1.

Authors:  K Inui; H Saito; R Hori
Journal:  Biochem J       Date:  1985-04-01       Impact factor: 3.857

Review 5.  Selected aspects of cell volume control in renal cortical and medullary tissue.

Authors:  M A Linshaw
Journal:  Pediatr Nephrol       Date:  1991-09       Impact factor: 3.714

6.  Hexose regulation of sodium-hexose transport in LLC-PK1 epithelia: the nature of the signal.

Authors:  A Moran; R J Turner; J S Handler
Journal:  J Membr Biol       Date:  1984       Impact factor: 1.843

7.  Ouabain binding in rectal gland of Squalus acanthias.

Authors:  P Silva; J A Epstein; A Stevens; K Spokes; F H Epstein
Journal:  J Membr Biol       Date:  1983       Impact factor: 1.843

8.  Modifications of anionic-lipid domains preceding membrane fusion in guinea pig sperm.

Authors:  E L Bearer; D S Friend
Journal:  J Cell Biol       Date:  1982-03       Impact factor: 10.539

  8 in total

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