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阳离子环境对高钾和低钾绵羊红细胞免疫溶血的影响。

Effect of the cationic environment on immune haemolysis of high potassium and low potassium sheep erythrocytes.

作者信息

De Bracco M M, Dalmasso A P

出版信息

Immunology. 1969 Oct;17(4):559-69.

Abstract

Immune haemolysis was studied with the two types of genetically controlled sheep erythrocytes (E) which contain either high potassium (K) and low sodium (Na) (HK E) or low K and high Na (LK E). It was found that the susceptibility of HK and LK E to lysis by guinea-pig and human complement is influenced by the cationic environment. In veronal buffer containing 0.140 M sodium, caesium, choline or Tris, HK E were less susceptible to immune lysis than LK E. No difference was observed in potassium and in lithium(Li). Immune lysis of HK E was stimulated by the cationic series: K>Li>Rb>Cs>Na. Immune lysis of LK E was less dependent on the cationic environment, but K had a slight stimulatory effect. HK and LK E had similar reactivity with haemolytic antibody and in immune adherence. The enhancing effect of potassium was demonstrable upon E (an erythrocyte which has been damaged by complement but has not yet undergone lysis), suggesting that the cationic effect is produced in the final steps of immune lysis. The data suggest that the different reactivity of HK and LK E with complement in a sodium medium might be independent of the cationic permeability properties of the membrane. Inhibition of active transport by ouabain did not modify the reactivity of HK and LK E with complement in a sodium medium.

摘要

利用两种基因控制的绵羊红细胞(E)研究免疫溶血,这两种红细胞分别含有高钾(K)低钠(Na)(HK E)或低钾高钠(LK E)。发现HK E和LK E对豚鼠及人补体溶解作用的敏感性受阳离子环境影响。在含有0.140M钠、铯、胆碱或Tris的巴比妥缓冲液中,HK E比LK E对免疫溶解更不易感。在钾和锂(Li)中未观察到差异。HK E的免疫溶解受阳离子系列刺激:K>Li>Rb>Cs>Na。LK E的免疫溶解对阳离子环境依赖性较小,但K有轻微刺激作用。HK E和LK E与溶血抗体及免疫黏附的反应性相似。钾对已受补体损伤但尚未发生溶解的E(红细胞)有增强作用,提示阳离子效应在免疫溶解的最后步骤产生。数据表明,HK E和LK E在钠介质中与补体的不同反应性可能与膜的阳离子通透性特性无关。哇巴因对主动转运的抑制并未改变HK E和LK E在钠介质中与补体的反应性。

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Sodium and potassium movements in human red cells.人体红细胞中钠和钾的运动
J Physiol. 1956 Nov 28;134(2):278-310. doi: 10.1113/jphysiol.1956.sp005643.

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