Cellular genes and signaling pathways as therapeutic targets for virus-induced CN

细胞基因和信号通路作为病毒诱导 CN 的治疗靶点

• 批准号: 8215547
• 负责人: Kenneth L. Tyler
• 金额: $ 34.43万
• 依托单位: UNIVERSITY OF COLORADO DENVER
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-15 至 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8215547
• 关键词: Acyclovir; Apoptosis; Apoptotic; Brain; Brain Injuries; Caspase; Caspase Inhibitor; Cell Death; Central Nervous System Diseases; Cessation of life; Clinical; Data; Disease; Encephalitis; Encephalitis Viruses; Evaluation; Experimental Models; Family; Genes; Genetic Transcription; Genetically Modified Animals; Goals; HIV; Herpes encephalitis; Hospitalization; In Vitro; Individual; Infection; Inflammatory Response; Microarray Analysis; Mitogen-Activated Protein Kinases; Modeling; Morbidity - disease rate; Mus; Neuroglia; Neurons; Nuclear Receptors; PPAR gamma; Pathway Analysis; Pathway interactions; Pattern; Peptide Hydrolases; Proteins; Receptor Signaling; Reoviridae Infections; Reovirus; Role; Signal Pathway; Signal Transduction; Signal Transduction Pathway; Signaling Pathway Gene; Simplexvirus; Source; System; Testing; Therapeutic; Tissue-Specific Gene Expression; Transcriptional Regulation; Viral; Viral Encephalitis; Viral Pathogenesis; Virus; Virus Diseases; West Nile virus; activating transcription factor; caspase-3; caspase-8; cell growth regulation; cellular targeting; clinically relevant; disability; human disease; in vivo; in vivo Model; inhibitor/antagonist; mortality; neuron loss; neurotropic; neurotropic virus; new therapeutic target; novel; receptor; research study; therapeutic target; transcription factor; treatment strategy

DESCRIPTION (provided by applicant): Viral encephalitis is a major source of morbidity and mortality both in the U.S. and throughout the world. Proven treatments for viral encephalitis are limited to only a few viruses and even when treatments exist (e.g. acyclovir for herpes simplex encephalitis) disability and death remain significant. Novel and broadly applicable strategies for the treatment of neurotropic viral infections are desperately needed. Using microarray analysis we identified death receptor signaling and peroxisome proliferator-activated receptor gamma (PPAR3) signaling as cellular signaling pathways that are significantly represented by the pattern of differential gene expression following infection of the brain with reovirus and West Nile virus (WNV), neurotropic viruses from different viral families. Preliminary data suggests that these pathways modulate virus- induced neuronal cell death and disease and provide novel therapeutic targets for viral encephalitis. In the proposed studies we will investigate the activation of these pathways following infection of the brain with reovirus, WNV and herpes simplex virus (HSV). Reovirus represents a "classic" in vivo experimental model of viral encephalitis. Complementary experiments using our recently developed ex vivo model of reovirus encephalitis and in vitro experiments with primary neuronal cultures provide an unmatched experimental system for the rapid evaluation of therapeutic targets for virus-induced CNS disease. To increase the impact and significance of our proposal we will perform parallel experiments with the clinically important encephalitic viruses, WNV and HSV. In order to identify novel cellular genes and pathways that can be used as therapeutic targets for viral encephalitis we will perform an inventive microarray approach using pairs of neurovirulent and neuroattenuated strains of reovirus, WNV and HSV. It is expected that genes and signaling pathways that are differentially regulated or activated following infection with neurovirulent and neuroattenuated viral strains will be directly involved in viral pathogenesis within the brain. Our experiments will thus identify a restricted set cellular genes and signaling pathways that will be evaluated as therapeutic targets for viral encephalitis. Identified genes and signaling pathways may be applicable as therapeutic targets for individual viruses. However, by identifying cellular factors that are differentially regulated following infection with multiple viruses from different families, we also expect to identify cellular targets with broad spectrum therapeutic potential for encephalitis induced by a variety of known and unknown (emerging) viruses. Our studies are also expected to increase our understanding of other human diseases characterized by the onset or disruption of neuronal death signaling. PUBLIC HEALTH RELEVANCE: Virus encephalitis results in significant morbidity and mortality throughout the world. Current treatment strategies which inhibit the replication of individual viruses are inadequate. We propose an alternate strategy to identify and evaluate novel therapeutic targets for virus-induced CNS disease from cellular genes and signaling pathways.

描述(申请人提供)：病毒性脑炎是美国和全世界发病率和死亡率的主要来源。已证实的治疗病毒性脑炎的方法仅限于少数几种病毒，即使存在治疗方法(如治疗单纯疱疹病毒性脑炎的阿昔洛韦)，残疾和死亡仍然很严重。迫切需要治疗嗜神经性病毒感染的新的和广泛适用的策略。通过基因芯片分析，我们发现死亡受体信号和PPAR3信号是细胞信号通路，在呼肠孤病毒和西尼罗河病毒(WNV)这两种不同病毒家族的嗜神经性病毒感染脑后的差异基因表达模式中表现出显著的差异。初步数据表明，这些通路调节病毒诱导的神经细胞死亡和疾病，并为病毒性脑炎提供新的治疗靶点。在拟议的研究中，我们将研究呼肠孤病毒、西尼罗河病毒和单纯疱疹病毒(HSV)感染大脑后这些途径的激活。呼肠孤病毒是一种典型的病毒性脑炎活体实验模型。使用我们最近开发的呼肠孤病毒脑炎体外模型的补充实验和原代神经元培养的体外实验为快速评估病毒诱导的中枢神经系统疾病的治疗靶点提供了一个无与伦比的实验系统。为了增加我们建议的影响和意义，我们将对临床上重要的脑炎病毒、西尼罗河病毒和单纯疱疹病毒进行平行实验。为了确定可用作病毒性脑炎治疗靶点的新的细胞基因和途径，我们将使用一对神经毒力和神经减毒的呼肠孤病毒、西尼罗河病毒和单纯疱疹病毒进行创造性的微阵列方法。人们预计，在感染神经毒力和神经减毒病毒株后，差异调节或激活的基因和信号通路将直接参与脑内病毒的发病。因此，我们的实验将确定一组受限的细胞基因和信号通路，这些基因和信号通路将被评估为病毒性脑炎的治疗靶点。已识别的基因和信号通路可能适用于作为个别病毒的治疗靶点。然而，通过确定在感染来自不同家族的多种病毒后存在差异调节的细胞因子，我们也希望确定具有广谱治疗潜力的细胞靶点，以治疗由各种已知和未知(新出现的)病毒引起的脑炎。我们的研究也有望增加我们对其他人类疾病的理解，这些疾病的特点是神经元死亡信号的开始或中断。 与公共卫生的相关性：病毒性脑炎在世界各地导致严重的发病率和死亡率。目前抑制单个病毒复制的治疗策略是不够的。我们提出了一种替代策略，从细胞基因和信号通路来确定和评估病毒诱导的中枢神经系统疾病的新治疗靶点。