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Role of the antiviral ribonuclease, RNase-L, in the host antibacterial response

抗病毒核糖核酸酶 RNase-L 在宿主抗菌反应中的作用

基本信息

批准号：
8317571
负责人：
BRET A HASSEL
金额：
$ 37.13万
依托单位：
UNIVERSITY OF MARYLAND BALTIMORE
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-08-15 至 2015-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8317571
关键词：
Affect Anti-Bacterial Agents Antibacterial Response Antiviral Agents Bacillus anthracis Bacteria Bacterial Infections Biological Biological Response Modifiers Cathepsin E Elements Escherichia coli Exhibits Foundations Gene Expression Regulation Goals Host Defense Immune Response Genes Immune response Immune system Immunity Integration Host Factors Interferons Light Mediating Mediator of activation protein Messenger RNA Microarray Analysis Molecular Mus Neutrophil Infiltration Pathway interactions Play Predisposition Process Public Health RNA Decay Regulation Ribonucleases Role Signal Pathway Signal Transduction Therapeutic Therapeutic Agents Trans-Activators Transcript Vacuole Wild Type Mouse antimicrobial base chemokine combat cytokine immune function mRNA Transcript Degradation macrophage mortality novel pathogen public health relevance response therapeutic target therapy development

项目摘要

DESCRIPTION (provided by applicant): Type 1 interferons (IFNs) were discovered as mediators of host antiviral functions, and were recently shown to play essential roles in the innate immune response to nonviral pathogens. Established effectors of IFN antiviral action may thus serve previously unrecognized roles in antibacterial immunity. To understand how IFN exerts its antibacterial activities, the identities and mechanisms of action of specific antibacterial effectors must be determined. Towards this goal, we identified a novel role for RNase-L, an IFN-regulated antiviral ribonuclease, in the host antibacterial response. RNase-L-/- mice exhibited a significant increase in mortality following bacterial challenge. The increased susceptibility of RNase-L-/- mice to bacterial challenge was due to a compromised immune response resulting in an increased bacterial load. Microarray analysis to identify RNase- L-regulated host transcripts that may mediate its antibacterial activity identified two classes of RNase-L- dependent gene regulation that affected transcripts encoding established immune mediators. Specifically, in RNase-L-/- macrophages: 1. basal expression of cathepsin-E (CatE), that mediates endolysosome-associated immune functions, was increased suggesting that this mRNA is an RNase-L substrate; and 2. bacteria-induced expression of proinflammatory cytokines and chemokines was diminished, suggesting that RNase-L indirectly impacts their expression via the modulation of upstream signaling pathway(s). Consistent with the altered CatE expression in RNase-L-/- macrophages, the endolysosome-mediated clearance of phagocytic vacuoles was disrupted following bacterial infection. Bacteria-induced signal transduction was impaired in RNase-L-/- macrophages, providing a mechanistic basis for the diminished cytokine and chemokine expression, and corresponding modulation of neutrophil recruitment. Based on these findings, we hypothesize that RNase-L exerts its antibacterial activity through multiple mechanisms including the regulation of CatE- mediated endolysosome functions, and the induction of host cytokines and chemokines. The goals of this proposal are to dissect the mechanisms by which RNase-L regulates the expression of host immune response genes (aims 1 and 2), and to determine the roles of this regulation in its antibacterial activity (aim 3). The antibacterial activity of RNase-L activators will also be examined. The proposed studies will provide the first information on the role of RNase-L in antibacterial activity, and will identify specific components of RNase-L action as targets for therapeutic modulation of the innate immune response. Public Health Relevance: Bacterial infections are a major public health problem, and the mechanisms by which the immune system combats bacterial infection are incompletely understood. The identification of key mediators of bacterial defense is essential for the development of therapies to enhance the antibacterial immune response. The proposed studies will provide the first information on the role of RNase-L as a novel mediator of antibacterial activity, and will evaluate the antibacterial activity of RNase-L activators as a new class of therapeutic agent.

描述（由申请人提供）：1型干扰素（ifn）被发现是宿主抗病毒功能的介质，最近被证明在对非病毒性病原体的先天免疫反应中发挥重要作用。因此，已确定的干扰素抗病毒作用效应物可能在抗菌免疫中起着以前未被认识到的作用。为了了解IFN如何发挥其抗菌活性，必须确定特定抗菌效应物的身份和作用机制。为了实现这一目标，我们确定了RNase-L（一种ifn调节的抗病毒核糖核酸酶）在宿主抗菌反应中的新作用。RNase-L-/-小鼠在细菌攻击后死亡率显著增加。RNase-L-/-小鼠对细菌攻击的易感性增加是由于免疫反应受损导致细菌负荷增加。微阵列分析鉴定了可能介导其抗菌活性的RNase- l调控宿主转录本，发现了两类RNase- l依赖性基因调控影响编码已建立的免疫介质的转录本。具体来说，在RNase-L-/-巨噬细胞中：介导内溶酶体相关免疫功能的组织蛋白酶e （CatE）的基础表达增加，表明该mRNA是RNase-L底物；和2。细菌诱导的促炎细胞因子和趋化因子的表达减少，表明RNase-L通过调节上游信号通路间接影响它们的表达。与RNase-L-/-巨噬细胞中CatE表达的改变一致，细菌感染后内溶酶体介导的吞噬空泡清除被破坏。细菌诱导的信号转导在RNase-L-/-巨噬细胞中受损，为细胞因子和趋化因子表达减少以及相应的中性粒细胞募集调节提供了机制基础。基于这些发现，我们推测RNase-L通过多种机制发挥其抗菌活性，包括调节CatE介导的内溶酶体功能，以及诱导宿主细胞因子和趋化因子。本提案的目标是剖析RNase-L调节宿主免疫反应基因表达的机制（目的1和2），并确定这种调节在其抗菌活性中的作用（目的3）。研究了RNase-L激活剂的抗菌活性。拟议的研究将提供关于RNase-L在抗菌活性中的作用的第一个信息，并将确定RNase-L作用的特定成分作为先天性免疫反应治疗性调节的靶点。公共卫生相关性：细菌感染是一个主要的公共卫生问题，免疫系统对抗细菌感染的机制尚不完全清楚。鉴定细菌防御的关键介质对于开发增强抗菌免疫反应的治疗方法至关重要。这些研究将首次提供RNase-L作为一种新的抗菌活性介质的作用信息，并将评估RNase-L激活剂作为一类新的治疗剂的抗菌活性。