Zika virus infection of neural stem cells to model pathogen-induced microcephaly
Zika virus infection of neural stem cells to model pathogen-induced microcephaly
批准号:
9266693
负责人:
Stacy Michelle Horner
金额:
$19.88万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-09-30 至 2018-08-31
关键词:
AddressApoptosisBehaviorBiological AssayBiologyBrainBrain InjuriesCell CycleCell SurvivalCell divisionCellsCellular AssayCenters for Disease Control and Prevention (U.S.)CytomegalovirusDataDevelopmentDiagnosticEmbryoEpidemicFlavivirusFunctional disorderGene ExpressionGeneticGenetic TranscriptionGrowthHandHealthHumanImageImmunofluorescence ImmunologicInfectionIntellectual functioning disabilityKnowledgeLifeLinkMessenger RNAMethodsMethylationMicrocephalyMitosisModelingModificationMolecularMolecular ProfilingMusNervous system structureNeurodevelopmental DisorderNeurogliaNeuronsOutcomePathogenesisPhenotypePopulationPregnancyProductionPublic HealthRNARNA VirusesSatellite VirusesSeveritiesSilverStagingTestingTherapeuticTranscriptVirusVirus ActivationVirus DiseasesVirus ReceptorsZika Virusbrain sizecell typefetalmRNA Expressionmouse modelnerve stem cellnervous system disorderneuropathologynovelpathogenpreventprospectivestem cell differentiationstem cell divisiontranscriptomeviral RNAvirology
中文摘要
寨卡病毒(ZIKV)是一种黄病毒属的RNA病毒,正在引起一种新出现的全球流行病。寨卡病毒感染与神经系统疾病密切相关,包括大脑大小严重缩小的先天性小头畸形。此外,疾控中心最近得出结论,寨卡病毒会导致小头症。寨卡病毒相关小头畸形的严重程度提示大脑发育受到早期损害。在人类小头症大脑中,寨卡病毒RNA已在神经元和前瞻性神经胶质细胞中检测到。在感染寨卡病毒的小鼠模型中,也在这些相同的人群中检测到病毒。寨卡病毒也被证明会感染神经干细胞,影响它们的生长和存活。在胎儿大脑发育的早期阶段,神经干细胞产生神经元,并随着发育的进行转变为胶质细胞的产生。神经干细胞功能障碍被认为是遗传性小头畸形的潜在原因。总的来说,这暗示了一种潜在的机制,可以解释为什么寨卡病毒同时感染神经元和神经胶质。在这一提议中,我们将测试寨卡病毒感染靶向胚胎神经干细胞,改变其细胞行为和转录组的假设。使用我们实验室开发的一套新颖的检测方法,我们将实现两个目标。首先,我们将确定寨卡病毒如何影响神经干细胞,包括产生新的可存活的后代。其次,我们将在神经干细胞中定义受ZIKV感染动态调控的宿主mrna。完成后,这些目标将阐明对寨卡病毒生物学的基本理解,特别是在发育中的神经系统中,这是开始控制寨卡病毒流行的重要信息。
英文摘要
Zika virus (ZIKV) is an RNA virus of the flavivirus genus that is causing an emerging global epidemic. ZIKV infection has been strongly associated with neurological disorders, including congenital microcephaly, in which brain size is severely reduced. Moreover the CDC has recently concluded that ZIKV causes microcephaly. The severity of ZIKV-associated microcephaly is suggestive of an early insult to brain development. In human microcephalic brains, ZIKV RNA has been detected in neurons and prospective glia. In mouse models of ZIKV infection, virus has also been detected in these same populations. ZIKV has also been shown to infect neural stem cells impacting their growth and survival. During early stages of fetal brain development, neural stem cells produce neurons and shift to glia production as development proceeds. Neural stem cell dysfunction is thought to be an underlying cause for genetic forms of microcephaly. Altogether this suggests a potential mechanism to explain why ZIKV infects both neurons and glia. In this proposal we will test the hypothesis that ZIKV infection targets embryonic neural stem cells, altering their cellular behavior and transcriptome. Using a novel set of assays developed in our labs, we will pursue two aims. First, we will determine how ZIKV impacts neural stem cells including production of new viable progeny. Second we will define the host mRNAs dynamically regulated by ZIKV infection in neural stem cells. Upon completion, these aims will elucidate a fundamental understanding of ZIKV biology, particularly within the developing nervous system, essential information for beginning to control the ZIKV epidemic.
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