Biorepository of Human iPSCs for Studying Dilated and Hypertrophic Cardiomyopathy
Biorepository of Human iPSCs for Studying Dilated and Hypertrophic Cardiomyopathy
批准号:
8838250
负责人:
ATUL J BUTTE
金额:
$173.42万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-04-15 至 2019-03-31
关键词:
AcademiaAddressAdultAreaBiologyBusinessesCardiacCardiac MyocytesCardiotoxicityCardiovascular DiseasesCardiovascular systemCell LineCellsChildhoodClinicClinical TrialsCommunitiesDNADataDevelopmentDevelopmental BiologyDilated CardiomyopathyDiseaseDrug IndustryFamilial Hypertrophic CardiomyopathyFeedbackFibroblastsFriendsFutureGenerationsGenesGenomicsGenotypeGoalsGrantHeart DiseasesHumanHypertrophic CardiomyopathyIndividualIndustryInheritedLaboratoriesMedicineMethodsMindMissionModelingMolecularMonoclonal Antibody R24MutationNational Heart, Lung, and Blood InstitutePatient RecruitmentsPatientsPharmaceutical PreparationsPhenotypePopulation GeneticsPreclinical Drug EvaluationRegenerative MedicineReproducibilityResearchResearch PersonnelResearch Project GrantsResource SharingResourcesSafetySamplingTechnologyTestingTimeUnited States National Institutes of HealthVisionabstractingbiobankbiomedical informaticscell bankclinical phenotypecohortdifferential expressiondrug discoverydrug marketgenetic variantgenome sequencingimprovedinduced pluripotent stem cellinterestlarge-scale databasemembermolecular phenotypemultidisciplinarynext generation sequencingnoveloutreach programrepositoryscreeningstem cell biologytranscriptome sequencing
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Familial dilated cardiomyopathy (DCM) and familial hypertrophic cardiomyopathy (HOM) are considered the two most common causes of inherited cardiovascular diseases. Previously, it has been difficult to study these diseases in human models because of limited access to human cardiomyocytes and difficulty growing them. With the discovery of human induced pluripotent stem cells (iPSCs) and the increased efficiency and reproducibility of differentiating them into beating cardiomyocytes (iPSC-CMs), the landscape has dramatically changed. For the first time, it is now possible to create patient-specific and disease-specific cell lines to improve our understanding of the molecular mechanisms of DCM and HCM.
Hence the major goals of this multidisciplinary R24 Resource-Related Research Project are (i) generation, (ii) characterization, (iii) sequencing, and (iv) distribution of cardiac iPSC lines. Over the next 5 years, we plan to create an iPSC bank of 600 lines derived from control individuals, HCM patients, and DCM patients. To accomplish these goals, we have assembled a truly collaborative team of investigators with expertise in cardiovascular medicine, iPSC biology, developmental biology, next generation sequencing (NGS) technology, population genetics, biomedical informatics, large-scale database repository, and business development. We propose the following 4 Specific Aims over the next 5 years:
Aim 1: To generate 600 iPSC lines from controls, DCM, and HCM patients.
Aim 2: To evaluate drug safety screening using iPSCs ("clinical trial in a petri dish").
Aim 3: To obtain genotype-phenotype information using DNA-seq and RNA-seq.
Aim 4: To distribute IPSC lines and their genotype-phenotype data to academic community.
In summary, we believe this R24 will address a national need and fulfill NHLBI's strategic vision of creating a novel biorepository (iPSC-genotype-phenotype) that is valuable to the broader scientific community. Given our expertise and track record, we are confident we can deliver on these milestones. (End of Abstract)
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海外基金