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一种用于定量可溶性CD163的猪特异性酶联免疫吸附测定法的开发与应用。

Development and application of a porcine specific ELISA for the quantification of soluble CD163.

作者信息

Pasternak J Alex, MacPhee Daniel J, Harding John C S

机构信息

Department of Large Animal Clinical Sciences, Western College of Veterinary Medicine, 52 Campus Dr., University of Saskatchewan, Saskatoon, SK, S7N 5B4, Canada.

Department Veterinary Biomedical Sciences, Western College of Veterinary Medicine, 52 Campus Dr., University of Saskatchewan, Saskatoon, SK, S7N 5B4, Canada.

出版信息

Vet Immunol Immunopathol. 2019 Apr;210:60-67. doi: 10.1016/j.vetimm.2019.03.011. Epub 2019 Mar 25.

Abstract

The cellular marker CD163 is a type 1 transmembrane scavenger protein found either on the surface of antigen-presenting cells or in a soluble form (sCD163), released in response to inflammation. Despite an obligatory role in porcine reproductive and respiratory virus (PRRSV) infection, information on sCD163 as a biomarker of disease outcome in swine remains limited. In the present study, we developed a sandwich ELISA using an anti-bovine CD163 antibody, LND68A, in conjunction with the porcine specific 2A10/11 antibody. The ELISA demonstrated that CD163 shedding from porcine alveolar macrophages increased following in vitro exposure to lipopolysaccharide or PRRSV-2 strain NVSL 97-7895. Evaluation of serum sCD163 in healthy feeder pigs identified a significant age effect with concentration rising after birth to a peak at day 19 (P < 0.05) followed by a sharp decline to a minimal level of detection at 9 weeks of age (P < 0.05). Healthy sows showed substantial variation but no significant change in average concentration between early and late lactation. The serum concentration of sCD163 from pigs with homozygous gene edits disrupting translation of the CD163 protein was below the threshold of detection. However, when reformatted as a competitive ELISA the assay identified an interfering substance consistent with the release of a truncated form of the CD163 protein in sera from gene edited animals. With sCD163 shown to be both dynamic and responsive, the described ELISA represents a novel tool for investigation of this molecule as a potential biomarker of disease response in the pig.

摘要

细胞标志物CD163是一种1型跨膜清道夫蛋白,存在于抗原呈递细胞表面或以可溶性形式(sCD163)存在,后者是在炎症反应时释放的。尽管CD163在猪繁殖与呼吸综合征病毒(PRRSV)感染中起重要作用,但关于sCD163作为猪疾病结局生物标志物的信息仍然有限。在本研究中,我们使用抗牛CD163抗体LND68A与猪特异性2A10/11抗体联合开发了一种夹心ELISA。该ELISA表明,体外暴露于脂多糖或PRRSV-2毒株NVSL 97-7895后,猪肺泡巨噬细胞的CD163脱落增加。对健康育肥猪血清sCD163的评估发现,存在显著的年龄效应,浓度在出生后上升至第19天达到峰值(P < 0.05),随后急剧下降至9周龄时的最低检测水平(P < 0.05)。健康母猪表现出较大差异,但在泌乳早期和晚期之间平均浓度无显著变化。纯合基因编辑破坏CD163蛋白翻译的猪的血清sCD163浓度低于检测阈值。然而,当将该检测方法重新设计为竞争性ELISA时,该检测方法鉴定出一种干扰物质,与基因编辑动物血清中截短形式的CD163蛋白释放一致。鉴于sCD163具有动态性和反应性,所描述的ELISA代表了一种新工具,可用于研究该分子作为猪疾病反应潜在生物标志物的情况。

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