Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen

被引:9
|
作者
Wyllie, David H. [1 ]
Sogaard, Karen C. [1 ]
Holland, Karen [2 ]
Xu Yaobo [3 ]
Bregu, Migena [1 ]
Hill, Adrian V. S. [1 ]
Kiss-Toth, Endre [2 ]
机构
[1] Univ Oxford, Jenner Inst, Oxford, England
[2] Univ Sheffield, Dept Cardiovasc Sci, Sheffield, S Yorkshire, England
[3] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England
来源
PLOS ONE | 2012年 / 7卷 / 07期
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; SIGNAL-TRANSDUCTION; CONTAINING ADAPTER; EXPRESSION; RECEPTOR; KINASE; FAMILY; ACTIVATION; POLYMORPHISM; REGULATOR;
D O I
10.1371/journal.pone.0042388
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Signal transduction pathways activated by Toll-like Receptors and the IL-1 family of cytokines are fundamental to mounting an innate immune response and thus to clearing pathogens and promoting wound healing. Whilst mechanistic understanding of the regulation of innate signalling pathways has advanced considerably in recent years, there are still a number of critical controllers to be discovered. In order to characterise novel regulators of macrophage inflammation, we have carried out an extensive, cDNA-based forward genetic screen and identified 34 novel activators, based on their ability to induce the expression of cxcl2. Many are physiologically expressed in macrophages, although the majority of genes uncovered in our screen have not previously been linked to innate immunity. We show that expression of particular activators has profound but distinct impacts on LPS-induced inflammatory gene expression, including switch-type, amplifier and sensitiser behaviours. Furthermore, the novel genes identified here interact with the canonical inflammatory signalling network via specific mechanisms, as demonstrated by the use of dominant negative forms of IL1/TLR signalling mediators.
引用
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页数:11
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