Conversion of Fibroblasts to fxnal Spinal Motor Neurons Using Defined Factor
Conversion of Fibroblasts to fxnal Spinal Motor Neurons Using Defined Factor
批准号:
8605244
负责人:
Justin Kawika Ichida
金额:
$24.9万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-01-01 至 2015-12-31
关键词:
AddressAdultAmyotrophic Lateral SclerosisCellsDNA MethylationDegenerative DisorderDisease modelDoctor of PhilosophyElectrophysiology (science)EmbryoEngineeringEpigenetic ProcessFibroblastsGene Expression ProfileGenerationsGoalsHumanIn VitroIndividualMediatingMolecularMorphologyMotor NeuronsMusNervous system structureNeurodegenerative DisordersNeuronsPatientsPhasePhenotypeProcessPropertyRegenerative MedicineResourcesRodentRouteSomatic CellSourceSpinalSpinal Muscular AtrophyStem cellsStimulusSynapsesTherapeuticTherapeutic UsesTimeabstractingcell typeembryonic stem cellin vivomotor neuron functionnerve stem celltranscription factortranslational study
中文摘要
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英文摘要
Abstract
The mammalian nervous system is composed of a multitude of distinct neuronal subtypes, each with
its own phenotype and differential sensitivity to degenerative disease. Although some specific neuronal types
can be isolated from intact rodent embryos or engineered from stem cells for translational studies, these
approaches are time-consuming and many neuronal subtypes are inaccessible. Transcription factor-mediated
reprogramming might provide a more direct route to the generation of neurons for disease modeling and
regenerative medicine, but it is currently unclear if this approach can be used to create cells with translational
utility. Here, we propose to identify a set of transcription factors sufficient to convert fibroblasts into
functional spinal motor neurons. We will characterize the reprogramming process and examine the molecular
and functional properties of the resulting motor neurons in order to determine their therapeutic potential.
These studies will provide an accessible source of patient-specific motor neurons for the study of
neurodegenerative disease, demonstrate that specific adult cell types can be directly generated from somatic
cells using defined factors, and mechanistically dissect the defined-factor reprogramming process.
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海外基金