Role of microglia in neural infection
Role of microglia in neural infection
批准号:
10391023
负责人:
Tian Wang
金额:
$51.61万
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-01-15 至 2026-12-31
关键词:
AbbreviationsAffectAnimal ModelB-Cell ActivationBiochemical GeneticsBiological AssayBrainCell DeathCell modelCellsCollaborationsDataDevelopmentDisease OutbreaksEmbryoEndoplasmic ReticulumEnhancersEquus caballusFetal Growth RetardationFetusFlavivirusGoalsGrowthHumanIRF3 geneImmuneImmunologyImpairmentIn VitroIncidenceInfectionInflammatoryInterferon-betaKnock-outKnockout MiceLeadLightMAP Kinase GeneMediatingMicrocephalyMicrogliaMitogen-Activated Protein KinasesMolecularMothersMusMyelogenousNeuraxisNeuronsNeurosciencesNewborn InfantNuclearOutcomeOutcome StudyPlayPolymerase Chain ReactionPreventionPrevention strategyProductionProtein-Serine-Threonine KinasesRIPK1 geneReportingRoleSourceSyndromeTLR3 geneTLR7 geneTLR8 geneTNF Receptor-Associated FactorsTRAF6 geneTestingTimeTranscription Factor AP-1UbiquitinVertical Disease TransmissionViralVirusVirus DiseasesYolk CellYolk SacZIKV infectionZika Virusbasebrain cellconditional knockoutcongenital zika syndromecytokinefetalgenetic manipulationhuman embryonic stem cellin vivoinfection rateinhibitor-of-apoptosis proteininnovationknock-downnerve stem cellneurogenesisprogenitorreceptorrelating to nervous systemresponsestemstem cell functionstem cellsteratogenesistreatment strategyubiquitin-protein ligaseviral transmission
中文摘要
摘要
寨卡病毒(ZIKV)感染与先天性ZIKV综合征(CZS)有关,包括各种脑异常
还有小头畸形症。我们最近的研究表明,卵黄囊(YS)来源的小胶质细胞(初级免疫细胞)
Peli1(一种E3泛素连接酶)与ZIKV感染及其相关的CZS有关。然而,它
目前尚不清楚Peli1是否以及如何在YS-小胶质细胞介导的ZIKV传播到大脑中起作用,是否
病毒感染影响小胶质细胞的正常功能,以及这种影响如何影响神经分化。
根据初步数据,我们假设Peli1在胎儿脑ZIKV感染中起关键作用。
通过改变小胶质细胞功能促进YS-小胶质细胞介导的ZIKV在胎脑中的传播
神经分化。这一假设将通过两个具体的目标进行检验:1)确定Peli1如何促进
ZIKV感染YS-小胶质细胞并将病毒从小胶质细胞传播到神经干细胞;
目的:探讨Peli1在ZIKV感染后如何介导小胶质细胞活化和改变神经分化。这
综合研究采用了体内动物模型和体外动物模型中的生化和遗传操作
小鼠和人类细胞平台。结果将通过分子、细胞和神经解剖学进行评估。
分析。了解小胶质细胞在ZIKV相关脑中作用的分子机制
感染可能导致确定预防和治疗寨卡病毒和其他病毒媒介的新靶点
先天性神经感染。
英文摘要
ABSTRACT
Zika virus (ZIKV) infection is associated with congenital ZIKV syndrome (CZS), including various brain anomalies
and microcephaly. Our recent studies suggested that yolk sac (YS)-derived microglia (primary immune cells in
the brain) and Peli1 (an E3 ubiquitin ligase) are involved in ZIKV infection and its associated CZS. However, it
is unknown whether and how Peli1 contributes to the YS-microglia-mediated spread of ZIKV into brain, whether
viral infection affects the normal function of microglia, and how such effects influence neural differentiation.
Based on preliminary data, we hypothesize that Peli1 plays a critical role in fetal brain ZIKV infection via
promoting YS-microglia-mediated ZIKV dissemination into fetal brain and via altering microglial function to affect
neural differentiation. This hypothesis will be tested by two specific aims: 1) to determine how Peli1 promotes
ZIKV infection of YS-microglia and virus dissemination from microglia to neural stem cells in fetal brains; and 2)
to determine how Peli1 mediates microglial activation and alters neural differentiation after ZIKV infection. This
integrative study employs biochemical and genetic manipulations in both in vivo animal models and in vitro
mouse and human cell platforms. The outcomes will be evaluated by molecular, cellular, and neuroanatomical
analyses. Understanding the molecular mechanisms underlying the role of microglia in ZIKV-related brain
infection may lead to identification of new targets for prevention and treatment of ZIKV and other virus-mediated
congenital neural infections.
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Role of microglia in neural infection
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