Oxygen-sensitive cation transport in sickle cells

被引:6
作者
Gibson, JS [1 ]
机构
[1] Univ London St Georges Hosp, Sch Med, Dept Physiol, London SW17 0RE, England
基金
英国惠康基金;
关键词
potassium; oxygen; KCI cotransport; sickle cell; polymerization; oxidant;
D O I
10.1006/bcmd.2000.0361
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There are many examples of O-2-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 O-2 may also be important pathologically. Significant alterations in O-2 dependence of red cell cation transport are observed in sickle cell disease land also following exposure to oxidants) and probably contribute to its pathophysiology. In this paper, we review some of the features of O-2-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. (C) 2001 Academic Press.
引用
收藏
页码:112 / 120
页数:9
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