Literature DB >> 19268612

Red blood cell Na pump: Insights from species differences.

Craig Gatto1, Mark Milanick.   

Abstract

The red blood cell membrane is specialized to exchange chloride and bicarbonate; usually the pH gradient, the chloride ratio, and the membrane potential are tightly coupled. We review the evidence that led to the ability to separately vary inside and outside pH in red cells. The effect of pH on Na pump activity and on the selectivity of the inside and the outside transport sites is reviewed. In red blood cells, at high pH, the outside site is not selective. An increase in protons leads to an increase in K(+) affinity, thus making the site more selective. The pK for this site is different in rats and humans; because of the high conservation of residues in these two species, there are only a few possible residues that can account for this difference. On the inside, work from unsided preparations suggests that, at high pH, the transport site is highly selective for Na(+). Once again, an increase in protons leads to an increase in K(+) affinity, but now the result is a less selective site. During their maturation, reticulocytes lose many membrane proteins. The type and fractional loss is species dependent. For example, most reticulocytes lose most of their Na pumps, retaining about 100 pumps per cell, but animals from the order Carnivora lose all their pumps. We review some of the evidence that PKC phosphorylation of N-terminus serines is responsible for endocytosis in other cell types and species variation in this region.

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Year:  2009        PMID: 19268612      PMCID: PMC2696618          DOI: 10.1016/j.bcmd.2009.01.011

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  43 in total

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Authors:  M L Jennings
Journal:  J Membr Biol       Date:  1976-08-26       Impact factor: 1.843

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Journal:  Mol Biol Cell       Date:  2000-01       Impact factor: 4.138

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Authors:  Syed Jalal Khundmiri; Alejandro M Bertorello; Nicholas A Delamere; Eleanor D Lederer
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Authors:  Mark A Milanick; Krista L Arnett
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6.  Bretylium, an organic quaternary amine, inhibits the Na,K-ATPase by binding to the extracellular K-site.

Authors:  Jeff B Helms; Krista L Arnett; Craig Gatto; Mark A Milanick
Journal:  Blood Cells Mol Dis       Date:  2004 May-Jun       Impact factor: 3.039

7.  The relationship between anion exchange and net anion flow across the human red blood cell membrane.

Authors:  P A Knauf; G F Fuhrmann; S Rothstein; A Rothstein
Journal:  J Gen Physiol       Date:  1977-03       Impact factor: 4.086

8.  Chemical modification of membranes. I. Effects of sulfhydryl and amino reactive reagents on anion and cation permeability of the human red blood cell.

Authors:  P A Knauf; A Rothstein
Journal:  J Gen Physiol       Date:  1971-08       Impact factor: 4.086

9.  Anion inhibitor-sensitive unidirectional sodium movements in the human erythrocyte.

Authors:  T J Callahan; D A Goldstein
Journal:  J Gen Physiol       Date:  1978-07       Impact factor: 4.086

10.  Electrophoretic separation of different phophosproteins associated with Ca-ATPase and Na, K-ATPase in human red cell ghosts.

Authors:  P A Knauf; F Proverbio; J F Hoffman
Journal:  J Gen Physiol       Date:  1974-03       Impact factor: 4.086

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6.  An Insight into the Stages of Ion Leakage during Red Blood Cell Storage.

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  6 in total

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