Mechanisms of neuronal injury during virus infection of the CNS

中枢神经系统病毒感染过程中神经元损伤的机制

• 批准号: 8077213
• 负责人: Charles Lee Howe
• 金额: $ 29.15万
• 依托单位: MAYO CLINIC ROCHESTER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-08-01 至 2013-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8077213
• 关键词: Acute; Address; Adoptive Transfer; Adult; Animals; Apoptotic; Ataxia; Biological Phenomena; Brain; Calcium; Calpain; Caspase; Cell Death; Cells; Central Nervous System Infections; Central Nervous System Viral Diseases; Cessation of life; Child; Cognitive; Complex; Coupled; Disease Outbreaks; Employee Strikes; Enterovirus 71; Equilibrium; FDA approved; Family Picornaviridae; Health; Hippocampus (Brain); Host Defense; Hour; Human; Image; Immune; Immune response; Immune system; Impaired cognition; Infection; Inflammation; Inflammatory; Inflammatory Response; Injury; Intervention; Life; Mediating; Memory; Modeling; Mus; Neuraxis; Neurologic; Neuronal Injury; Neurons; Neutrophil Infiltration; Peptide Hydrolases; Performance; Pharmaceutical Preparations; Picornaviridae Infections; Population; Risk; Role; Seizures; TMEV; Testing; Therapeutic Intervention; Uncertainty; Viral; Virus; Virus Diseases; Work; base; calpain inhibitor; cognitive function; foodborne; global health; hippocampal pyramidal neuron; immunopathology; innovation; killings; mouse model; neuron apoptosis; neuron loss; neurotoxic; neutrophil; novel therapeutics; prevent; response; trafficking; waterborne

DESCRIPTION (provided by applicant): Foodborne and waterborne picornaviruses such as enterovirus 71 are a global health issue. Neurologic complications associated with neurovirulent non-polio picornavirus infection are a serious ongoing health problem, especially in children. Unfortunately, the mechanisms of picornavirus-induced injury to the central nervous system (CNS) are unclear. We propose that the innate immune response is an important cause of neuron death during acute infection. This is in contrast to the prevailing hypothesis that neuron loss is mediated solely by virus. While we do not doubt that some neurons die directly as the result of viral infection, our preliminary findings suggest that certain populations, such as CA1 pyramidal neurons in the hippocampus, are killed by the innate immune response rather than by the virus. We have established a mouse model of picornavirus infection of the CNS using the Theiler's murine encephalomyelitis virus to directly test the role of neutrophils in the initiation of neuronal apoptosis. Our preliminary evidence indicates that during acute picornaviral infection of the CNS, many uninfected CA1 pyramidal neurons undergo apoptotic death associated with oxidative injury, calpain activity, and caspase activity; this injury severely reduces cognitive performance in a spatial memory test. We have further observed that neutrophils infiltrate the hippocampus within hours of infection. Reduced neutrophil infiltration is neuroprotective, while adoptive transfer of activated neutrophils into mice with a defective neutrophil response induces hippocampal injury. Finally, treatment with calpain inhibitors protects hippocampal neurons from death and preserves cognitive function without constraining the inflammatory response that is necessary to mediating host defense and viral clearance. On the basis of these observations we hypothesize that neutrophils kill hippocampal neurons via a calpain-dependent mechanism during acute picornaviral infections of the CNS. We intend to address the following experimental questions: 1) are neutrophils necessary and sufficient to kill hippocampal neurons?; 2) is calpain the key executioner of hippocampal neurons during death induced by the neutrophil response to acute CNS infection? We propose several innovations, including the use of live animal imaging and adoptive transfer of neutrophils, to address these questions. The key concept of our proposal is that while inflammation critically mediates host defense to virus infection, the inflammatory response may indirectly kill neurons, and therefore therapeutic interventions aimed at preventing neuronal death without thwarting inflammatory control of virus may preserve host function. PUBLIC HEALTH RELEVANCE: Certain foodborne and waterborne viruses have the ability to infect the brain. Although adults are susceptible, children are at particular risk for such neurovirulent infections. We have evidence from a mouse model that cognitive function is lost concomitantly with the death of hippocampal neurons. We also have evidence that this neuronal death is caused by a specific population of immune cells called neutrophils that are trying to clear the virus from the brain. Importantly, we have found that treatment with an FDA-approved drug protects neurons and cognitive function without altering the ability of the immune system to clear the virus from the brain.

描述（由申请方提供）：食源性和水媒小核糖核酸病毒，如肠道病毒71是一个全球性的健康问题。与神经毒性非脊髓灰质炎小核糖核酸病毒感染相关的神经并发症是一个严重的持续健康问题，特别是在儿童中。不幸的是，小核糖核酸病毒引起的中枢神经系统（CNS）损伤的机制尚不清楚。我们认为先天免疫反应是急性感染时神经元死亡的一个重要原因。这与普遍的假设形成鲜明对比，即神经元损失仅由病毒介导。虽然我们并不怀疑某些神经元直接死于病毒感染，但我们的初步研究结果表明，某些群体，如海马体中的CA1锥体神经元，是由先天免疫反应而不是病毒杀死的。我们已经建立了一个小鼠模型的小核糖核酸病毒感染的中枢神经系统使用Theiler的小鼠脑脊髓炎病毒，直接测试的作用，中性粒细胞在神经元凋亡的启动。我们的初步证据表明，在急性小核糖核酸病毒感染的中枢神经系统，许多未感染的CA1锥体神经元发生凋亡与氧化损伤，钙蛋白酶活性，半胱天冬酶活性，这种损伤严重降低了认知能力的空间记忆测试。我们进一步观察到，中性粒细胞在感染后数小时内浸润海马体。减少中性粒细胞浸润是神经保护性的，而过继转移活化的中性粒细胞到有缺陷的中性粒细胞反应的小鼠诱导海马损伤。最后，钙蛋白酶抑制剂治疗保护海马神经元免于死亡，并保留认知功能，而不限制介导宿主防御和病毒清除所必需的炎症反应。基于这些观察结果，我们推测在中枢神经系统急性小核糖核酸病毒感染期间，中性粒细胞通过钙蛋白酶依赖性机制杀死海马神经元。我们打算解决以下实验问题：1）嗜中性粒细胞是否是杀死海马神经元的必要和充分条件？2)钙蛋白酶是急性中枢神经系统感染引起的中性粒细胞死亡过程中海马神经元的关键执行者吗？我们提出了几个创新，包括使用活体动物成像和过继转移中性粒细胞，以解决这些问题。我们建议的关键概念是，虽然炎症介导宿主对病毒感染的防御，但炎症反应可能间接杀死神经元，因此旨在防止神经元死亡而不阻碍病毒的炎症控制的治疗干预可能会保护宿主功能。公共卫生相关性：某些食源性和水媒病毒具有感染大脑的能力。尽管成年人易感，但儿童感染此类神经病毒的风险尤其大。我们从小鼠模型中得到的证据表明，认知功能的丧失伴随着海马神经元的死亡。我们也有证据表明，这种神经元死亡是由一种称为嗜中性粒细胞的特定免疫细胞群引起的，这些细胞试图将病毒从大脑中清除。重要的是，我们发现，使用FDA批准的药物治疗可以保护神经元和认知功能，而不会改变免疫系统从大脑中清除病毒的能力。