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Hematopoiesis from Normal and Patient-Derived Induced Pluripotent Stem Cells

Hematopoiesis from Normal and Patient-Derived Induced Pluripotent Stem Cells
正常和患者来源的诱导多能干细胞的造血作用
批准号:
7853198
负责人:
Mitchell J Weiss
金额:
$99.72万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2011-08-31
关键词:
Acute Megakaryocytic LeukemiasAddressAffectAreaArtsBiochemical GeneticsBioethicsBioinformaticsBiologyBiomedical ResearchBloodBlood CellsCD34 geneCellsCellular MorphologyChildChildhoodChromatinClinicClinicalClinical MedicineCollaborationsComplementDataDevelopmentDiamond-Blackfan anemiaDiseaseDown SyndromeEmbryoEmerging TechnologiesEpigenetic ProcessErythroErythroblastsErythroidErythropoiesisFetal LiverFoundationsFunctional disorderFutureGATA1 geneGene ExpressionGene TransferGenesGenomeGerm LayersGerm-Line MutationHeartHematological DiseaseHematologyHematopoiesisHematopoieticHereditary DiseaseHistocompatibility TestingHumanImmunodeficient MouseIn VitroIndividualInstitutesInstitutionLaboratoriesLongitudinal StudiesLungMedical ResearchMethodsModelingModificationMutationNational Heart, Lung, and Blood InstituteNew EnglandNormal tissue morphologyOccupationsPatientsPatternPediatric HospitalsPennsylvaniaPhenotypePhiladelphiaPredispositionPreleukemiaProceduresProcessProductionProtocols documentationRegulatory AffairsResearchResearch InfrastructureResearch PersonnelResourcesRibosomal ProteinsSolidSomatic CellSomatic MutationSourceTechnologyTissuesTransfusionTransplantationUmbilical Cord BloodUniversitiesWorkbasecell bankcell typecollegedesigndisease phenotypeembryonic stem cellexperiencefetalgenetic manipulationhematopoietic tissuehomologous recombinationhuman GATA1 proteinhuman diseaseinduced pluripotent stem cellinfancyinterestleukemianew technologynovelnovel therapeutic interventionpractical applicationprogenitorpublic health relevanceregenerative therapyrepositoryresearch studytooltransient myeloproliferative disorder

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DESCRIPTION (provided by applicant): This project addresses the NHLBI RC2 GO application entitled "Characterizing Differentiated Heart, Lung, and Blood Cells Derived by Reprogramming Human Embryonic and Induced Pluripotent Stem Cells." Emerging technologies to generate induced pluripotent stem cells (iPSCs) by reprogramming human somatic cells promises to revolutionize biomedical research and clinical medicine. Through in vitro culture methods, iPSCs can be differentiated into numerous cells types derived from all three germ layers. This raises the possibility that patient-derived iPSCs can be used to create relevant tissues for the study of many human disorders. In addition, iPSCs may provide starting material to manufacture transplantable cells for transfusion and regenerative therapies. However, the field is in its infancy and many core questions must be solved in order to realize these exciting long-term prospects. This proposal seeks to advance the use of iPSCs for the study of normal and pathological hematopoiesis. Multiple investigators with broad areas of expertise in hematopoiesis, embryonic stem cell/iPSC biology, chromatin biology, clinical hematology, bioinformatics, cell banking and bioethics/regulatory affairs will work together to pursue the following global issues 1) Mechanisms by which hematopoietic developmental potential might vary between different normal iPSC clones; 2) The extent to which iPSC-derived hematopoietic precursors resemble normal ones with respect to cellular phenotypes, gene expression and epigenetic signatures; 3) Whether hematopoietic disease phenotypes can be recapitulated by in vitro manipulation of patient-derived iPSCs. We will execute these studies using novel methods to create and culture iPSCs and state-of-the art tools to analyze and manipulate their resident genomes. Pursuit of these problems will serve as a framework in which to develop a facile infrastructure where investigators at our large pediatric institution can create, analyze, bank and distribute iPSCs from any patient of interest. If successful, this work will help to accelerate practical applications of iPSCs for the study and treatment of human diseases. This work will be based at Children's Hospital of Philadelphia with subcontracts to The Pennsylvania State University (State College, PA) and The Coriell Institute for Medical Research (Camden, NJ). The project will create 6 new jobs, thereby stimulating the economy in three different regions of the Northeastern United States. PUBLIC HEALTH RELEVANCE: Efforts to better understand blood production from patient-derived induced pluripotent stem cells (iPSCs) will enhance our understanding of blood disorders and generate new therapeutic approaches. Additionally, this work could create new general paradigms for studying the genesis of many normal tissues and their associated diseases.
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ULK-mediated autophagy of α-globin in ß-thalassemia
ULK-mediated autophagy of α-globin in ß-thalassemia
Core B: Human Stem Cell Core
  • 批准号:
    8698736
  • 项目类别:
  • 资助金额:
    $41.1万
  • 财政年份:
    2014
  • 负责人:
    Mitchell J Weiss
  • 依托单位:
Trim58 and the Ubiquitin Proteasome System in Erythro-megakaryopoiesis
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