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镰状细胞病中的红细胞膜异常。

Erythrocyte membrane abnormalities in sickle cell disease.

作者信息

Williamson P, Puchulu E, Westerman M, Schlegel R A

机构信息

Amherst College, Massachusetts 01002.

出版信息

Biotechnol Appl Biochem. 1990 Oct;12(5):523-8.

PMID:2288707
Abstract

A large fraction of circulating sickle red cells contain one or more large vesicles which are not found in normal erythrocytes. These vesicles contain very high levels of Ca2+, and probably account for the long-known elevation of cellular Ca2+ in sickle cells. These vesicles contain the plasma membrane CaATPase and leak Ca2+ by a nitrendipine-sensitive pathway. The question of whether an abnormal endocytic process occurs in sickle cells which could give rise to these vesicles was examined using the nonspecific endocytic marker Lucifer yellow (LY). The kinetics of formation of LY-labeled endocytic vesicles in sickle cells includes a slow component which is not found in normal (or sickle) reticulocytes. In addition, the number of sickle cells in which endocytosis can be demonstrated with this nonspecific marker consistently exceeds the number which can be labeled with markers of the receptor-mediated endocytic process. The results suggest that a slow, abnormal endocytosis takes place in sickle cells which may be the source of the Ca2(+)-containing vesicles, and therefore of the elevated Ca2+ levels characteristic of the circulating cells in this disease.

摘要

循环中的镰状红细胞很大一部分含有一个或多个在正常红细胞中未发现的大囊泡。这些囊泡含有非常高的Ca2+水平,可能是镰状细胞中细胞Ca2+长期升高的原因。这些囊泡含有质膜CaATPase,并通过尼群地平敏感途径泄漏Ca2+。使用非特异性内吞标记物路西法黄(LY)研究了镰状细胞中是否发生异常内吞过程从而产生这些囊泡的问题。镰状细胞中LY标记的内吞囊泡形成动力学包括一个正常(或镰状)网织红细胞中未发现的缓慢成分。此外,用这种非特异性标记物可证明发生内吞作用的镰状细胞数量始终超过用受体介导的内吞过程标记物可标记的细胞数量。结果表明,镰状细胞中发生了缓慢的异常内吞作用,这可能是含Ca2+囊泡的来源,因此也是该疾病循环细胞中Ca2+水平升高的特征来源。

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