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测量小鼠补体途径的总经典途径及各组分活性。

Measuring Total Classical Pathway and Activities of Individual Components of the Mouse Complement Pathway.

作者信息

Zelek Wioleta M

机构信息

Division of Infection and Immunity and Dementia Research Institute, School of Medicine, Cardiff University, Wales, United Kingdom.

出版信息

Bio Protoc. 2021 Oct 5;11(19):e4175. doi: 10.21769/BioProtoc.4175.

Abstract

The complement system is a central component of innate immunity, responsible for recognition and killing of bacteria by tagging invaders through opsonisation, thereby promoting phagocytosis, and by direct lysis. Complement activity is routinely measured using functional assays that utilise erythrocytes as targets. The classical pathway haemolytic assay (CH50) with antibody sensitised sheep erythrocytes as target is used worldwide in clinical and research laboratories to measure complement activity in human and rodent sera. While there are no particular limitations in the human assay, measuring complement in mouse serum is more difficult and usually requires large amounts of serum, which is challenging to collect in experiments. In particular, it is challenging to measure the activities of individual mouse complement proteins. To overcome this hurdle, we have developed protocols that employ human sera depleted of single complement proteins as the source of the other complement proteins and test mouse serum to restore the relevant component. This simple haemolytic assay is a useful tool for confirming natural or engineered complement deficiencies and complement dysregulation in mouse models.

摘要

补体系统是固有免疫的核心组成部分,通过调理作用标记入侵者来识别和杀灭细菌,从而促进吞噬作用,并通过直接裂解发挥作用。补体活性通常使用以红细胞为靶标的功能测定法进行测量。以抗体致敏绵羊红细胞为靶标的经典途径溶血测定法(CH50)在全球临床和研究实验室中用于测量人和啮齿动物血清中的补体活性。虽然人体检测没有特别限制,但测量小鼠血清中的补体更为困难,通常需要大量血清,这在实验中收集具有挑战性。特别是,测量单个小鼠补体蛋白的活性具有挑战性。为了克服这一障碍,我们开发了一些方案,采用去除单一补体蛋白的人血清作为其他补体蛋白的来源,并检测小鼠血清以恢复相关成分。这种简单的溶血测定法是确认小鼠模型中天然或工程化补体缺陷及补体失调的有用工具。

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Mol Immunol. 2019 Oct;114:341-352. doi: 10.1016/j.molimm.2019.07.030. Epub 2019 Aug 22.
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