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单克隆抗体可保护多形核白细胞免受补体攻击。

Monoclonal antibodies demonstrate protection of polymorphonuclear leukocytes against complement attack.

作者信息

Campbell A K, Morgan B P

出版信息

Nature. 1985;317(6033):164-6. doi: 10.1038/317164a0.

Abstract

Studies on erythrocytes have shown that the formation of the membrane attack complex on a cell surface inevitably results in lysis. However, it is known that nucleated cells are much more difficult to kill with complement, although the molecular basis of this resistance has never been established. We have shown that a very early intracellular event, occurring within seconds of formation of the attack complex in the membrane, is a rise in cytoplasmic Ca2+, which can activate cell responses without cell death 5,6. Here we report the use of a monoclonal antibody to the terminal complement component C9, quantified by 125I and visualized by fluorescein, to demonstrate a protection mechanism in polymorphonuclear leukocytes (PMNs) attacked by complement, involving removal of the attack complex by vesiculation. Concomitantly, there is a Ca2+-dependent activation of reactive oxygen metabolite production without cell lysis. These findings have important implications in the evolutionary and pathological significance of the terminal components of the complement pathway.

摘要

对红细胞的研究表明,在细胞表面形成膜攻击复合物不可避免地会导致细胞裂解。然而,已知有核细胞更难被补体杀死,尽管这种抗性的分子基础尚未确定。我们已经表明,在膜中攻击复合物形成后的几秒钟内发生的一个非常早期的细胞内事件是细胞质Ca2+的升高,这可以激活细胞反应而不导致细胞死亡5,6。在这里,我们报告使用一种针对末端补体成分C9的单克隆抗体,通过125I定量并用荧光素可视化,以证明在受到补体攻击的多形核白细胞(PMN)中的一种保护机制,该机制涉及通过囊泡化去除攻击复合物。同时,在没有细胞裂解的情况下,会有Ca2+依赖性的活性氧代谢产物产生的激活。这些发现对补体途径末端成分的进化和病理意义具有重要影响。

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