Exosomal miRNA in neuron to astroglial communication in the CNS
Exosomal miRNA in neuron to astroglial communication in the CNS
批准号:
10621422
负责人:
Yongjie Yang
金额:
$6.27万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-07-01 至 2023-06-30
关键词:
AddressAdultAffectAstrocytesAwardAxonBiologicalBlood VesselsBrainCaliberCell CommunicationCellsCellular biologyCentral Nervous System DiseasesCoculture TechniquesCommunicationComplement 1qConceptionsCre driverDataDevelopmentEndosomesExanthemaExerciseGeneticGenetic TranscriptionGlioblastomaGlutamate TransporterImageImmuneIn SituIn VitroInjectionsKnowledgeLabelLearningLigandsLocationMalignant NeoplasmsMediatingMicroRNAsModelingMolecularMonitorMorphogenesisMorphologyMotor NeuronsMusNervous System TraumaNeurodegenerative DisordersNeurogliaNeuronsNeurotransmittersPHluorinPathologicPathway interactionsPhysiologyPresynaptic TerminalsProcessPublishingRegulationResearchRetinal Ganglion CellsRoleSamplingSignal TransductionSpinalSurfaceSynapsesSynaptic TransmissionTechniquesTestingUnited States National Institutes of HealthVesiclebasecareer developmentcell typedesigner receptors exclusively activated by designer drugsexosomeexperimental studyextracellular vesiclesfluorescence imaginggenome-widein vivoinsightintercellular communicationintravitreal injectionmyelinationnervous system disorderneuronal cell bodyneurotransmitter releasenotch proteinnovelpolarized cellreceptorsciatic nervesynaptic functiontranscriptome
中文摘要
总结
这一多样性补充旨在提供一个机会,拉希德阿兰泽谁满足国家卫生研究院
多样性候选人标准,在我的实验室进行学士后研究。在这个项目中,Rashed将
表征神经元外泌体从索马或轴突终末的分泌以及随后的
神经元外泌体内化为星形胶质细胞。虽然管腔内囊泡(ILV),前体
分泌的外泌体,主要定位于培养神经元的体树突区室,这是未知的
这些ILV是否优先从体内神经元索马或轴突分泌,考虑到囊泡
神经递质的分泌主要从轴突末梢释放。利用坐骨神经
注射模型以选择性标记脊髓运动神经元(SMN)外泌体和玻璃体内注射以选择性
标记视网膜神经节细胞(RGC),Rashed将专门研究和比较神经元外泌体是否
从体树突或轴突终末隔室差异释放,这些
外泌体也不同地被周围的星形胶质细胞摄取。
了解外泌体分泌的主要位置从这样一个极化的细胞类型,如神经元
将对这些外来体的潜在功能提供重要的见解。通过实施该项目,
他有机会了解如何看到一个项目,从概念到完成,学习各种注射
技术,处理科学实验中总是需要的故障排除和优化,
学习分析图像和数据的最佳方法。总的来说,这一多样性补充奖将大大准备
急着发展他的研究事业。
英文摘要
Summary
This diversity supplement aims to provide an opportunity for Rashed Alananzeh who meets the NIH
diversity candidate criteria, to carry out a post-Baccalaureate study in my lab. In this project, Rashed will
characterize the secretion of neuronal exosomes from either soma or axon terminals and the subsequent
internalization of neuronal exosomes into astrocytes. Although intraluminal vesicles (ILVs), precursors for
secreted exosomes, are largely localized in the somatodendritic compartment of cultured neurons, it is unknown
whether these ILVs are preferentially secreted from neuronal soma or axons in vivo, given that vesicular
secretion of neurotransmitters are predominantly released from axon terminals. By employing sciatic nerve
injection model to selectively label spinal motor neuron (SMN) exosomes and intravitreal injection to selectively
label retina ganglion cells (RGC), Rashed will specifically investigate and compare whether neuronal exosomes
are differentially released from either somatodendritic or axon terminal compartments and whether these
exosomes are also differentially taken up into surrounding astrocytes.
Understanding the predominant location of exosome secretion from such a polarized cell type as neurons
will give important insights into the potential function of those exosomes. By carrying out this project, it will give
him the opportunity to understand how to see a project through from conception to finish, learn various injection
techniques, deal with the troubleshooting and optimization that are always needed in scientific experiments and
learn the best ways to analyze images and data. Overall, this diversity supplement award will greatly prepare
Rashed for his research career development.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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海外基金