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促红细胞生成素可使人类骨髓细胞内的游离钙迅速增加。

Erythropoietin induces rapid increases in intracellular free calcium in human bone marrow cells.

作者信息

Mladenovic J, Kay N E

机构信息

Department of Medicine, University of Minnesota, Minneapolis.

出版信息

J Lab Clin Med. 1988 Jul;112(1):23-7.

PMID:3260614
Abstract

Elevation of intracellular free calcium (Ca++) is an early activation event that occurs as a result of ligand binding in several human cell systems. In this report, erythropoietin, the major hormone governing erythroid differentiation, was found to elicit an increase in Ca++ in human bone marrow mononuclear cells. Two chelators of intracellular calcium, quin 2 and the more specific and sensitive analogue, fura-2, were used to characterize the response evoked by both recombinant and native hormone. Erythropoietin caused a rapid, dose-dependent rise (within seconds) in Ca++ in bone marrow mononuclear cells, which could be prevented by preincubation of hormone with a rabbit erythropoietin antiserum. The erythropoietin response did not occur in purified populations of T- or B-lymphocytes. These studies suggested that increased Ca++ on erythropoietin binding may be an early transmembrane signal in hormone action.

摘要

细胞内游离钙(Ca++)水平升高是早期激活事件,它是由几种人类细胞系统中的配体结合引起的。在本报告中,发现促红细胞生成素(调控红细胞生成的主要激素)可引起人骨髓单个核细胞中Ca++增加。使用两种细胞内钙螯合剂喹啉2以及更特异和敏感的类似物呋喃2来表征重组激素和天然激素所引发的反应。促红细胞生成素可使骨髓单个核细胞中的Ca++迅速、剂量依赖性升高(数秒内),用兔促红细胞生成素抗血清预孵育激素可阻止这种升高。在纯化的T淋巴细胞或B淋巴细胞群体中未出现促红细胞生成素反应。这些研究表明,促红细胞生成素结合后Ca++增加可能是激素作用中的早期跨膜信号。

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