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红细胞膜蛋白带4.2:表型、遗传学及电子显微镜学方面

Red cell membrane protein band 4.2: phenotypic, genetic and electron microscopic aspects.

作者信息

Yawata Y

机构信息

Department of Medicine, Kawasaki Medical School, Kurashiki, Japan.

出版信息

Biochim Biophys Acta. 1994 Feb 16;1204(2):131-48. doi: 10.1016/0167-4838(94)90001-9.

Abstract

The present status of band 4.2 has been reviewed from the standpoint of protein chemistry, gene analysis and clinical hematology. Band 4.2 plays an important role in various cellular functions. In 142 GCT-->ACT band 4.2 deficiency, abnormalities of the cytoskeletal network were clearly observed by electron microscopy and by ektacytometry, although the cytoskeletal proteins themselves were essentially normal in these red cells. The physiological states of band 3 in situ in the membranes were also affected in band 4.2 deficiency, as detected by electron microscopy, although again the biochemical properties of band 3 itself were essentially normal in these red cells. Other disorders of band 4.2 deficiency in the absence of the 142 GCT-->ACT mutation appear to be most interesting in the pathogenesis of hemolysis. In some of the band 4.2 anomalies, other membrane proteins including band 3 would appear to be most pathognomonic for the disease states. These conditions require elucidation by protein chemistry and gene analysis. The control mechanism of the gene expression should also be clarified to understand the important role of band 4.2 in health and disease.

摘要

从蛋白质化学、基因分析和临床血液学的角度对4.2带的现状进行了综述。4.2带在各种细胞功能中发挥着重要作用。在142 GCT→ACT 4.2带缺乏症中,通过电子显微镜和红细胞变形性测定法可清楚观察到细胞骨架网络的异常,尽管这些红细胞中的细胞骨架蛋白本身基本正常。通过电子显微镜检测发现,在4.2带缺乏症中,膜中3带的原位生理状态也受到影响,尽管这些红细胞中3带本身的生化特性基本正常。在没有142 GCT→ACT突变的情况下,4.2带缺乏症的其他病症在溶血发病机制中似乎最令人感兴趣。在一些4.2带异常中,包括3带在内的其他膜蛋白似乎对疾病状态最具诊断意义。这些情况需要通过蛋白质化学和基因分析来阐明。为了解4.2带在健康和疾病中的重要作用,还应阐明基因表达的控制机制。

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