Literature DB >> 11358370

Oxygen-sensitive cation transport in sickle cells.

J S Gibson1.   

Abstract

There are many examples of O2-sensitive solute transport in vertebrate red cells. The response is selective, specific, and conserved across the entire vertebrate spectrum. A number of possible physiological roles have been proposed, but abnormal responses to O2 may also be important pathologically. Significant alterations in O2 dependence of red cell cation transport are observed in sickle cell disease (and also following exposure to oxidants) and probably contribute to its pathophysiology. In this paper, we review some of the features of O2-sensitive solute transporters in red cells and possible reasons for the abnormal response in sickle cells. Our aim is to identify specific, novel pharmacological inhibitors of these abnormal pathways and thereby ameliorate the disease. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11358370     DOI: 10.1006/bcmd.2000.0361

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


  5 in total

1.  The effect of deoxygenation on whole-cell conductance of red blood cells from healthy individuals and patients with sickle cell disease.

Authors:  Joseph A Browning; Henry M Staines; Hannah C Robinson; Trevor Powell; J Clive Ellory; John S Gibson
Journal:  Blood       Date:  2006-11-30       Impact factor: 22.113

2.  The effect of xanthine oxidase and hypoxanthine on the permeability of red cells from patients with sickle cell anemia.

Authors:  Halima W M Al Balushi; David C Rees; John N Brewin; Anke Hannemann; John S Gibson
Journal:  Physiol Rep       Date:  2018-03

3.  Effects of 5-hydroxymethyl-2-furfural on the volume and membrane permeability of red blood cells from patients with sickle cell disease.

Authors:  Anke Hannemann; Urszula M Cytlak; David C Rees; Sanjay Tewari; John S Gibson
Journal:  J Physiol       Date:  2014-07-11       Impact factor: 5.182

4.  Identification of the Ca²⁺ entry pathway involved in deoxygenation-induced phosphatidylserine exposure in red blood cells from patients with sickle cell disease.

Authors:  U M Cytlak; A Hannemann; D C Rees; J S Gibson
Journal:  Pflugers Arch       Date:  2013-06-18       Impact factor: 3.657

5.  Cation Homeostasis in Red Cells From Patients With Sickle Cell Disease Heterologous for HbS and HbC (HbSC Genotype).

Authors:  A Hannemann; D C Rees; S Tewari; J S Gibson
Journal:  EBioMedicine       Date:  2015-09-18       Impact factor: 8.143

  5 in total

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