Induced Pluripotent Stem Cell Core for NiNDS Investigators
Induced Pluripotent Stem Cell Core for NiNDS Investigators
批准号:
8453519
负责人:
JOHN A KESSLER
金额:
$47.18万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-30 至 2017-06-30
关键词:
AchievementAdoptedAnatomyAstrocytesBiochemicalBiological AssayBiologyBrainCell DeathCell LineCellsCellular NeurobiologyCellular biologyCommunitiesComplementCuesDementiaDepositionDevelopmentDirect CostsDiseaseEducational process of instructingFibroblastsFunctional disorderFundingGenotypeGoalsHandHumanHuman Cell LineHuman ResourcesHuntington DiseaseImageIndividualInstitutesInstructionInvestmentsMedical RecordsMorphologyMotor Neuron DiseaseNanotechnologyNational Institute of Neurological Disorders and StrokeNervous System TraumaNervous system structureNeurodegenerative DisordersNeurogliaNeuronsNeurosciencesNeurosciences ResearchOligodendrogliaParkinson DiseasePatientsPhenotypePhysiologicalPluripotent Stem CellsPropertyProteinsRegenerative MedicineResearchResearch PersonnelSkinSomatic CellSpinal CordSpinocerebellar AtaxiasStem cellsSynaptic TransmissionTechniquesTechnologyTranslatingTransplantationUncertaintyUniversitiesbasebrain cellcell typedisorder controlhuman diseaseinduced pluripotent stem cellinsightnerve stem cellnervous system developmentnervous system disorderneurotransmitter releasenew technologyoverexpressionprogramsregenerativerepairedrepositorystem cell biologytissue culturevoltage clamp
中文摘要
产品说明:将体细胞重编程为多能干细胞(诱导多能干细胞-iPSC)的能力改变了基础人类细胞神经生物学的研究和人类神经系统疾病的细胞基础的检查。该技术使得研究人类神经干细胞、许多人类神经元表型以及人类星形胶质细胞和少突胶质细胞的发育和细胞生物学成为可能。此外,来自患有各种神经系统疾病的患者的体细胞可以被重新编程,以允许研究具有患病个体的基因型的神经元和神经胶质。毫无疑问,从这些研究中获得的见解将转化为更好的治疗方法,并最终治愈神经系统疾病。这项提案的战略目标是将这项关键技术交给NU一个高产的神经科学家小组,该小组目前从NINDS获得近600万美元(直接成本)的资金。具体来说,该中心将:1。提供设施和专业知识,使NINDS研究人员能够培养和分化人类iPSC,并使他们能够利用Coriell研究所和其他地方的细胞库。新的iPSC细胞系将根据NINDS研究人员的计划需要创建,这些细胞系将存放在Coriell Institute 2的NINDS人类细胞系库中。提供设施和专业知识来定义分化的iPSC的表型,包括iPSC衍生的神经元和神经胶质的形态,电学和其他特性。3.使NINDS研究人员能够在他们的研究计划中利用NU开发的新纳米技术进步来创建和分析iPSCs。这些目标的实现不仅将对NINDS资助的研究项目产生变革性影响,并利用NINDS的投资,而且还将大大加快这些技术向更广泛的神经科学界的交付,加快科学发现的步伐,促进神经系统疾病新疗法的开发。
英文摘要
DESCRIPTION: The ability to reprogram somatic cells into pluripotent stem cells (induced pluripotent stem cells - iPSCs) has transformed both the study of basic human cellular neurobiology and the examination of the cellular basis of human diseases of the nervous system. This technology makes it possible to study the development and cell biology of human neural stem cells, numerous human neuronal phenotypes, and human astrocytes and oligodendroglia. Further, somatic cells from patients with a variety of neurological diseases can be reprogrammed to allow study of neurons and glia with the genotypes of the afflicted individuals. There is no doubt that insights gained from such studies will translate into better treatments and eventually cures for neurological diseases. The strategic goal of this proposal is to put this critical technology into the hands of a highly productive group of neuroscientists at NU that currently receive nearly $6 million (direct costs) in funding from NINDS. Specifically the Center will: 1. Provide the facilities and expertise to enable NINDS investigators to culture and differentiate human iPSCs and to enable them to take advantage of cell repositories at the Coriell Institute and elsewhere. New iPSC lines will be created as needed for programs of NINDS investigators, and these lines will be deposited in the NINDS human cell line repository at the Coriell Institute 2. Provide the facilities and expertise to define the phenotype of differentiated iPSCs including morphology, electrical and other properties of iPSC-derived neurons and glia. 3. Enable NINDS investigators to utilize in their research programs new nanotechnology advances developed at NU for the creation and analysis of iPSCs. The attainment of these goals will not only have a transforming impact on the NINDS-funded research programs at NU and leverage the NINDS investment, but will also significantly accelerate the delivery of these technologies to the broader neuroscience community, quicken the pace of scientific discovery and promote the development of new treatments for neurological disorders.
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会议论文
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