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二维液相色谱-串联质谱联用等相对和绝对定量同位素标记技术(iTRAQ)标记方法揭示了猪圆环病毒 2 感染肺泡巨噬细胞的蛋白质组图谱。

Two-dimensional liquid chromatography-tandem mass spectrometry coupled with isobaric tags for relative and absolute quantification (iTRAQ) labeling approach revealed first proteome profiles of pulmonary alveolar macrophages infected with porcine circovirus type 2.

机构信息

Key Laboratory of Animal Diseases Diagnostic and Immunology, Ministry of Agriculture, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095,China.

出版信息

J Proteomics. 2013 Feb 21;79:72-86. doi: 10.1016/j.jprot.2012.11.024. Epub 2012 Dec 11.

DOI:10.1016/j.jprot.2012.11.024
PMID:23238063
Abstract

Porcine circovirus type 2 (PCV2) has been identified as the essential causal agent of postweaning multisystemic wasting syndrome, which has spread worldwide. Monocyte/macrophage lineage cells are the major target cells of PCV2. To discover cellular protein responses of pulmonary alveolar macrophages (PAMs) to PCV2 infection, two-dimensional liquid chromatography-tandem mass spectrometry coupled with isobaric tags for relative and absolute quantification (iTRAQ) labeling was employed to quantitatively identify the proteins that were differentially expressed in PAMs from the PCV2-infected group compared to the uninfected control group. A total of 145 cellular proteins in PAMs that were significantly altered at different time periods post-infection were identified. These differentially expressed proteins were related to the biological processes of binding, cell structure, signal transduction, cell adhesion, etc., and their interactions. The high number of differentially expressed proteins identified should be very useful to elucidate the mechanism of replication and pathogenesis of PCV2 in the future.

摘要

猪圆环病毒 2 型(PCV2)已被确定为断奶后多系统消耗综合征(PMWS)的主要致病因子,该疾病已在全球范围内传播。单核细胞/巨噬细胞谱系细胞是 PCV2 的主要靶细胞。为了发现肺肺泡巨噬细胞(PAMs)对 PCV2 感染的细胞蛋白反应,采用二维液相色谱-串联质谱联用等离 子标记定量技术(iTRAQ)标记来定量鉴定 PCV2 感染组与未感染对照组的 PAMs 中差异表达的蛋白质。在感染后不同时间点,共鉴定出 145 种在 PAMs 中显著改变的细胞蛋白。这些差异表达的蛋白质与结合、细胞结构、信号转导、细胞黏附等生物学过程及其相互作用有关。未来,这些鉴定出的大量差异表达蛋白对于阐明 PCV2 的复制和发病机制应该非常有用。

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