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用于阐明溶酶体在微生物感染中关键作用的定量蛋白质组学分析

Quantitative proteomic profiling for clarification of the crucial roles of lysosomes in microbial infections.

作者信息

Xu Benhong, Gao Yanpan, Zhan Shaohua, Ge Wei

机构信息

Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, National Key Laboratory of Medical Molecular Biology & Department of Immunology, No 5 Dongdan Santiao, Dongcheng District, Beijing 100005, China.

Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, National Key Laboratory of Medical Molecular Biology & Department of Immunology, No 5 Dongdan Santiao, Dongcheng District, Beijing 100005, China.

出版信息

Mol Immunol. 2017 Jul;87:122-131. doi: 10.1016/j.molimm.2017.04.002. Epub 2017 Apr 25.

Abstract

Lysosomes play vital roles in both innate and adaptive immunity. It is widely accepted that lysosomes do not function exclusively as a digestive organelle. It is also involved in the process of immune cells against pathogens. However, the changes in the lysosomal proteome caused by infection with various microbes are still largely unknown, and our understanding of the proteome of the purified lysosome is another obstacle that needs to be resolved. Here, we performed a proteomic study on lysosomes enriched from THP1 cells after infection with Listeria monocytogenes (L.m), Herpes Simplex Virus 1 (HSV-1) and Vesicular Stomatitis Virus (VSV). In combination with the gene ontology (GO) analysis, we identified 284 lysosomal-related proteins from a total of 4560 proteins. We also constructed the protein-protein interaction networks for the differentially expressed proteins and revealed the core lysosomal proteins, including SRC in the L. m treated group, SRC, GLB1, HEXA and HEXB in the HSV-1 treated group and GLB1, CTSA, CTSB, HEXA and HEXB in the VSV treated group, which are involved in responding to diverse microbial infections. This study not only reveals variable lysosome responses depending on the bacterial or virus infection, but also provides the evidence based on which we propose a novel approach to proteome research for investigation of the function of the enriched organelles.

摘要

溶酶体在先天性免疫和适应性免疫中都发挥着至关重要的作用。人们普遍认为,溶酶体并非仅仅作为一种消化细胞器发挥作用。它还参与免疫细胞对抗病原体的过程。然而,各种微生物感染所引起的溶酶体蛋白质组的变化在很大程度上仍不为人所知,而且我们对纯化溶酶体蛋白质组的了解是另一个需要解决的障碍。在此,我们对单核细胞增生李斯特菌(L.m)、单纯疱疹病毒1型(HSV-1)和水疱性口炎病毒(VSV)感染后的THP1细胞中富集的溶酶体进行了蛋白质组学研究。结合基因本体(GO)分析,我们从总共4560种蛋白质中鉴定出284种与溶酶体相关的蛋白质。我们还构建了差异表达蛋白质的蛋白质-蛋白质相互作用网络,并揭示了核心溶酶体蛋白,包括L.m处理组中的SRC、HSV-1处理组中的SRC、GLB1、HEXA和HEXB以及VSV处理组中的GLB1、CTSA、CTSB、HEXA和HEXB,它们参与对多种微生物感染的应答。这项研究不仅揭示了溶酶体根据细菌或病毒感染而产生的可变反应,还提供了证据,在此基础上我们提出了一种用于研究富集细胞器功能的蛋白质组学研究新方法。

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