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遗传性球形红细胞增多症中红细胞血影蛋白部分缺乏

Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.

作者信息

Agre P, Casella J F, Zinkham W H, McMillan C, Bennett V

出版信息

Nature. 1985;314(6009):380-3. doi: 10.1038/314380a0.

Abstract

Hereditary spherocytosis (HS) is a common, clinically heterogeneous haemolytic anaemia in which the primary erythrocyte defect is believed to be some abnormality in the spectrin-actin membrane skeleton, leading to loss of surface membrane. Recessively inherited spectrin deficiency with extreme erythrocyte fragility and spherocytosis has been identified in certain mutant mice and two severely anaemic humans. Although suspected, deficiency of spectrin has not been demonstrated in less severe forms of human HS. We not report the quantitation of erythrocytes spectrin by radioimmunoassay. We found that normal erythrocytes contained 240,000 copies of spectrin heterodimer, whereas erythrocytes from 14 patients with a variety of types of HS were all partially deficient in spectrin (range 74,000-200,000 copies), the magnitude of the deficiency correlating with the severity of the disease. Spectrin deficiency of varying degrees is common in HS and probably represents the principal structural defect leading to loss of surface membrane.

摘要

遗传性球形红细胞增多症(HS)是一种常见的、临床异质性溶血性贫血,其中原发性红细胞缺陷被认为是血影蛋白 - 肌动蛋白膜骨架存在某种异常,导致表面膜丢失。在某些突变小鼠和两名严重贫血的人类中已鉴定出隐性遗传的血影蛋白缺乏症,伴有极度红细胞脆性和球形红细胞增多症。虽然有所怀疑,但在症状较轻的人类HS中尚未证实血影蛋白缺乏。我们现在报告通过放射免疫测定法定量红细胞血影蛋白。我们发现正常红细胞含有240,000个血影蛋白异二聚体拷贝,而来自14例各种类型HS患者的红细胞血影蛋白均部分缺乏(范围为74,000 - 200,000个拷贝),缺乏程度与疾病严重程度相关。不同程度的血影蛋白缺乏在HS中很常见,可能是导致表面膜丢失的主要结构缺陷。

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