Literature DB >> 2260643

Swelling-activated KCl cotransport in rabbit red cells: flux is determined mainly by cell volume rather than shape.

M L Jennings1, R K Schulz.   

Abstract

The effect of cell shape on ouabain-insensitive 86Rb+ fluxes was examined in rabbit red blood cells. The purpose of the study was to assess the role of mechanical deformations of the membrane in the activation of KCl cotransport by cell swelling. Conversion of cells to echinocytes with low concentrations of amphiphilic agents (anionic and cationic detergents and dipyridamole) in an isotonic medium activates KCl cotransport only very slightly. Hypotonic swelling of echinocytes causes a large increase in KCl cotransport flux just as in swollen discocytes; both the rate and the extent of activation are unaffected by the shape change. Stomatocyte (cup cell) formation with 20 microM chlorpromazine in isotonic medium causes slight activation of KCl cotransport. The KCl cotransport flux induced by cell swelling is approximately 20% higher in swollen stomatocytes than in swollen discocytes. It is concluded that major changes in cell shape have only minor effects on the swelling sensor, signal transduction apparatus, and KCl cotransport protein. We interpret these findings as evidence against the idea that the cell detects its volume by way of a membrane-associated mechanical sensor. As an alternative to a mechanical volume sensor, a hypothetical mechanism for swelling activation of transport is presented in which dilution of the cytoplasm, by mass action alone, can have very large effects on KCl cotransport.

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Year:  1990        PMID: 2260643     DOI: 10.1152/ajpcell.1990.259.6.C960

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  11 in total

1.  Volume-sensitive K(+)/Cl(-) cotransport in rabbit erythrocytes. Analysis of the rate-limiting activation and inactivation events.

Authors:  M L Jennings
Journal:  J Gen Physiol       Date:  1999-12       Impact factor: 4.086

2.  Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes.

Authors:  Clinton H Joiner; R Kirk Rettig; Maorong Jiang; Mary Risinger; Robert S Franco
Journal:  Blood       Date:  2006-10-05       Impact factor: 22.113

3.  Tyrosine kinase activation is an immediate and essential step in hypotonic cell swelling-induced ERK activation and c-fos gene expression in cardiac myocytes.

Authors:  J Sadoshima; Z Qiu; J P Morgan; S Izumo
Journal:  EMBO J       Date:  1996-10-15       Impact factor: 11.598

Review 4.  Membrane transport of Na and K and cell dehydration in sickle erythrocytes.

Authors:  C Brugnara
Journal:  Experientia       Date:  1993-02-15

5.  Membrane stress increases cation permeability in red cells.

Authors:  R M Johnson
Journal:  Biophys J       Date:  1994-11       Impact factor: 4.033

6.  KCl cotransport activation in human erythrocytes by high hydrostatic pressure.

Authors:  H Godart; J C Ellory
Journal:  J Physiol       Date:  1996-03-01       Impact factor: 5.182

7.  Stimulation of KCl co-transport in equine erythrocytes by hydrostatic pressure: effects of kinase/phosphatase inhibition.

Authors:  J S Gibson; A C Hall
Journal:  Pflugers Arch       Date:  1995-01       Impact factor: 3.657

8.  Swelling activation of K-Cl cotransport in LK sheep erythrocytes: a three-state process.

Authors:  P B Dunham; J Klimczak; P J Logue
Journal:  J Gen Physiol       Date:  1993-05       Impact factor: 4.086

9.  Intracellular Cl- dependence of Na-H exchange in barnacle muscle fibers under normotonic and hypertonic conditions.

Authors:  E M Hogan; B A Davis; W F Boron
Journal:  J Gen Physiol       Date:  1997-11       Impact factor: 4.086

10.  Okadaic acid inhibition of KCl cotransport. Evidence that protein dephosphorylation is necessary for activation of transport by either cell swelling or N-ethylmaleimide.

Authors:  M L Jennings; R K Schulz
Journal:  J Gen Physiol       Date:  1991-04       Impact factor: 4.086

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