Bruce Lesley
Bristol Institute for Transfusion Sciences, National Blood Service, Southmead, Bristol BS10 5ND, UK.
Blood Cells Mol Dis. 2006 May-Jun;36(3):331-6. doi: 10.1016/j.bcmd.2006.01.008. Epub 2006 Mar 10.
We have recently shown that amino acid substitutions in the membrane domain of band 3 (anion exchanger 1, SLC4A1) are associated with hereditary stomatocytosis (HSt), a red cell condition in which the cells leak sodium and potassium ions. These substitutions appear to convert band 3 from an anion exchanger into a cation channel. In this review, I will first give some background on the structure and function of normal band 3 and describe our findings in red cells from HSt patients. Then I will compare the properties of the HSt band 3 to those of Southeast Asian Ovalocytosis (SAO) band 3 and discuss the implications for the structure of band 3, the quality control of protein expression in red cells and the cation permeability of normal human red cells.
我们最近发现,带3(阴离子交换蛋白1,SLC4A1)膜结构域中的氨基酸取代与遗传性口形红细胞增多症(HSt)相关,HSt是一种红细胞疾病,患病细胞会泄漏钠和钾离子。这些取代似乎将带3从阴离子交换蛋白转变为阳离子通道。在这篇综述中,我将首先介绍正常带3的结构和功能背景,并描述我们在HSt患者红细胞中的发现。然后,我将比较HSt带3与东南亚椭圆形红细胞增多症(SAO)带3的特性,并讨论其对带3结构、红细胞中蛋白质表达的质量控制以及正常人类红细胞阳离子通透性的影响。