Mechanisms of apoptosis in the central nervous system

中枢神经系统细胞凋亡的机制

• 批准号: 7000454
• 负责人: Kenneth L. Tyler
• 金额: $ 25.61万
• 依托单位: UNIVERSITY OF COLORADO DENVER
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-01-01 至 2009-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7000454
• 关键词: BCL2 gene /protein; Reoviridae; apoptosis; biological signal transduction; central nervous system; gene expression; immunocytochemistry; laboratory mouse; microarray technology; mitogen activated protein kinase; neurotropic virus; phosphorylation; polymerase chain reaction; virus diseases; western blottings

DESCRIPTION (provided by applicant): Viral infection of the central nervous system (CNS) is associated with a variety of neurologic diseases including meningitis, encephalitis, and myelitis, which have substantial morbidity and mortality and for which successful treatments are limited. The events that lead to virus-induced cell death, tissue injury and disease are not clearly understood. An increased understanding of the mechanisms by which neurotropic viruses kill cells in the CNS is thus a critical factor in the design of new therapeutic strategies. Apoptosis has been implicated as a mechanism of virus-induced CNS disease. In this proposal apoptotic signaling pathways and the regulation of these pathways will be investigated following viral infection of the CNS. Reovirus infection of neonatal mice and cultured neurons, which has proved to be one of the most important models for studying viral pathogenesis in the CNS, will be used for these studies. The role of virus-induced mitogen activated protein kinases (specific aim 1), transcription factors (specific aim 2) and gene expression changes (specific aim 3) will be investigated during death receptor and mitochondrial apoptotic signaling following reovirus infection of neuronal cells. In specific aim 3 non-targeted (microarray analysis), in addition to targeted, approaches will be used in order to elucidate novel viral mechanisms of CNS pathogenesis. Taken together these studies are designed to identify the regulation of apoptotic signaling during virus-induced apoptosis of the CNS. They are expected to have direct therapeutic implications for the development of novel therapies for CNS disease.

描述（由申请方提供）：中枢神经系统（CNS）的病毒感染与多种神经系统疾病相关，包括脑膜炎、脑炎和脑炎，这些疾病的发病率和死亡率很高，成功的治疗方法有限。导致病毒诱导的细胞死亡、组织损伤和疾病的事件尚不清楚。因此，对嗜神经性病毒杀死CNS细胞的机制的进一步理解是设计新治疗策略的关键因素。细胞凋亡已被认为是病毒诱导的中枢神经系统疾病的一种机制。在这个提议中，细胞凋亡信号通路和这些通路的调节将在病毒感染CNS后进行研究。新生小鼠和培养的神经元的呼肠孤病毒感染将用于这些研究，该模型已被证明是研究CNS中病毒发病机制的最重要模型之一。将研究呼肠孤病毒感染神经元细胞后死亡受体和线粒体凋亡信号传导过程中病毒诱导的有丝分裂原活化蛋白激酶（特异性目的1）、转录因子（特异性目的2）和基因表达变化（特异性目的3）的作用。在具体目标3中，除了靶向方法外，还将使用非靶向方法（微阵列分析）来阐明CNS发病机制的新病毒机制。总之，这些研究旨在确定病毒诱导的CNS细胞凋亡过程中细胞凋亡信号的调节。他们预计将有直接的治疗意义的开发新的治疗中枢神经系统疾病。