Literature DB >> 10578012

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

M L Jennings1.   

Abstract

The kinetics of activation and inactivation of K(+)/Cl(-) cotransport (KCC) have been measured in rabbit red blood cells for the purpose of determining the individual rate constants for the rate-limiting activation and inactivation events. Four different interventions (cell swelling, N-ethylmaleimide [NEM], low intracellular pH, and low intracellular Mg(2+)) all activate KCC with a single exponential time course; the kinetics are consistent with the idea that there is a single rate-limiting event in the activation of transport by all four interventions. In contrast to LK sheep red cells, the KCC flux in Mg(2+)-depleted rabbit red cells is not affected by cell volume. KCC activation kinetics were examined in cells pretreated with NEM at 0 degrees C, washed, and then incubated at higher temperatures. The forward rate constant for activation has a very high temperature dependence (E(a) approximately 32 kCal/mol), but is not affected measurably by cell volume. Inactivation kinetics were examined by swelling cells at 37 degrees C to activate KCC, and then resuspending at various osmolalities and temperatures to inactivate most of the transporters. The rate of transport inactivation increases steeply as cell volume decreases, even in a range of volumes where nearly all the transporters are inactive in the steady state. This finding indicates that the rate-limiting inactivation event is strongly affected by cell volume over the entire range of cell volumes studied, including normal cell volume. The rate-limiting inactivation event may be mediated by a protein kinase that is inhibited, either directly or indirectly, by cell swelling, low Mg(2+), acid pH, and NEM.

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Year:  1999        PMID: 10578012      PMCID: PMC2230653          DOI: 10.1085/jgp.114.6.743

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  54 in total

1.  Model for the role of macromolecular crowding in regulation of cellular volume.

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Authors:  S J Kelley; P B Dunham
Journal:  Am J Physiol       Date:  1996-04

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Authors:  M L Jennings
Journal:  J Membr Biol       Date:  1978-06-09       Impact factor: 1.843

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5.  Role of protein phosphatase in activation of KCl cotransport in human erythrocytes.

Authors:  D M Kaji; Y Tsukitani
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Review 6.  Volume-activated cation transport in dog red cells: detection and transduction of the volume stimulus.

Authors:  J C Parker
Journal:  Comp Biochem Physiol Comp Physiol       Date:  1992-08

7.  K-Cl cotransport in rabbit red cells: further evidence for regulation by protein phosphatase type 1.

Authors:  L C Starke; M L Jennings
Journal:  Am J Physiol       Date:  1993-01

8.  Taurine, betaine, and inositol share a volume-sensitive transporter in skate erythrocyte cell membrane.

Authors:  L Goldstein; E M Davis
Journal:  Am J Physiol       Date:  1994-08

9.  Magnesium buffering in intact human red blood cells measured using the ionophore A23187.

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Journal:  J Physiol       Date:  1980-08       Impact factor: 5.182

10.  Kinetics of activation and inactivation of swelling-stimulated K+/Cl- transport. The volume-sensitive parameter is the rate constant for inactivation.

Authors:  M L Jennings; N al-Rohil
Journal:  J Gen Physiol       Date:  1990-06       Impact factor: 4.086

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  11 in total

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Review 2.  Regulation of K-Cl cotransport: from function to genes.

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

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8.  Chemical crosslinking studies with the mouse Kcc1 K-Cl cotransporter.

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Journal:  Blood Cells Mol Dis       Date:  2009 May-Jun       Impact factor: 3.039

9.  Activation of Na+/H+ and K+/H+ exchange by calyculin A in Amphiuma tridactylum red blood cells: implications for the control of volume-induced ion flux activity.

Authors:  Alejandro Ortiz-Acevedo; Robert R Rigor; Hector M Maldonado; Peter M Cala
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10.  Identification of regulatory phosphorylation sites in a cell volume- and Ste20 kinase-dependent ClC anion channel.

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Journal:  J Gen Physiol       Date:  2008-12-15       Impact factor: 4.086

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