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由化合物4880和卵清蛋白诱导的非过敏性超敏反应的蛋白质组学研究。

Proteomics Study on Nonallergic Hypersensitivity Induced by Compound 4880 and Ovalbumin.

作者信息

Xu Yubin, Guo Na, Dou Deqiang, Ran Xiaoku, Ma Xiande, Kuang Haixue

机构信息

College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, Liaoning, China.

Experimental Research Center, China Academy of Chinese Medical Sciences, Beijing, China.

出版信息

PLoS One. 2016 Feb 1;11(2):e0148262. doi: 10.1371/journal.pone.0148262. eCollection 2016.

Abstract

Nonallergic hypersensitivity reaction (NHR) accounts for more than 77% of all immune-mediated immediate hypersensitivity reactions and has become a serious threat to public health. Here, proteomics was used to study the NHR mechanism of two typical substances, the compound 4880 and ovalbumin. Twelve different proteins were suggested as potential biomarkers for examining the NHR mechanism, and our results revealed that the mechanism mainly encompassed 2 processes, i.e., generation and effect processes. The generation process could be classified as direct stimulation, complement (classical and alternative), coagulation, kallikrein-kinin, and integrated pathways. Thus glutathione peroxidase 1, terminal complement complex (complement factor 4d and Bb), coagulation 13, kininogen-1, and IgE could be used as candidate biomarkers for the indication of the corresponding pathways respectively, the proteins were further confirmed by ELISA. And the effect process was mainly composed of histamine as well as proteins such as DCD and MYLPF, which could be used as important indices for the symptoms of NHR. Our study differs from previous studies in that C4880 was found to not only be involved in the direct stimulation pathway, but also in the activated complement and kallikrein-kinin pathways through the coagulation pathway. We also report for the first time that ovalbumin-induced NHR could be a combination of the coagulation, classical complement, and integrated pathways.

摘要

非过敏性超敏反应(NHR)占所有免疫介导的速发型超敏反应的77%以上,已对公众健康构成严重威胁。在此,蛋白质组学被用于研究两种典型物质——化合物48/80和卵清蛋白的NHR机制。有12种不同的蛋白质被认为是用于研究NHR机制的潜在生物标志物,我们的结果表明该机制主要包括2个过程,即生成过程和效应过程。生成过程可分为直接刺激、补体(经典和替代)、凝血、激肽释放酶-激肽和整合途径。因此,谷胱甘肽过氧化物酶1、末端补体复合物(补体因子4d和Bb)、凝血因子13、激肽原-1和IgE可分别用作指示相应途径的候选生物标志物,这些蛋白质通过酶联免疫吸附测定(ELISA)进一步得到证实。而效应过程主要由组胺以及DCD和MYLPF等蛋白质组成,它们可作为NHR症状的重要指标。我们的研究与以往研究的不同之处在于,发现化合物48/80不仅参与直接刺激途径,还通过凝血途径参与激活的补体和激肽释放酶-激肽途径。我们还首次报道卵清蛋白诱导的NHR可能是凝血、经典补体和整合途径的组合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c85/4734762/e6960b50898e/pone.0148262.g001.jpg

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