Dzip1 and Mitral Valve Prolapse
Dzip1 and Mitral Valve Prolapse
批准号:
10613538
负责人:
Russell Norris
金额:
$49.93万
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:
2020-06-01 至 2024-05-31
关键词:
AffectAnimal ModelArrhythmiaBiochemicalBiologicalBiomechanicsCardiovascular systemCiliaClinicalComplexCongestive Heart FailureDataDefectDetectionDevelopmentDiseaseDockingEndocarditisEtiologyExperimental GeneticsFailureFamilyFibrosisFoundationsFutureGenerationsGenesGeneticGenetic EpistasisGoalsHealthHeart AtriumHeart Valve DiseasesHeart ValvesHeart failureHumanHuman GeneticsHyperplasiaImageIn VitroIndividualInterventionKnock-inKnock-in MouseLeadLesionLightLinkMechanicsMedialMedicalMembraneMitral ValveMitral Valve InsufficiencyMitral Valve ProlapseMolecularMorbidity - disease rateMusMutationNatural regenerationNuclearOperative Surgical ProceduresPathogenesisPathway interactionsPatientsPeptidesPhenotypePopulationPopulation StudyProcessPtosisReporterSignal TransductionSudden DeathSystoleTechniquesTestingTherapeuticTissuesUnited StatesValidationVentricularVesicleWorkantagonistbasebeta catenincardiogenesiscilium biogenesisconditional knockoutgenetic approachgenetic variantimprovedin vivoinduced pluripotent stem cellinsightkinetosomemortalitymouse modelnovelnovel therapeuticspeptidomimeticsrestraintsudden cardiac deathtrafficking
中文摘要
项目总结
基于PI实验室和他的合作者所做的基因和细胞发现,这项建议侧重于
对心脏瓣膜形成至关重要的新机制。提案中提供的数据表明,
DZIP1基因的突变会导致一种非常常见的心脏瓣膜疾病(即二尖瓣脱垂),并可能
由发育过程中瓣膜组织形成方式的错误引起。这些发现导致了一种新的概念
纤毛参与瓣膜的发育。因此,我们的建议评估了纤毛在发育过程中的形成。
以及DZIP1如何在发育过程中调节纤毛发生和/或β-连环蛋白的活性。我们的
研究将提供独特的机会来回答迄今已有的有关心脏瓣膜疾病的问题。
即使使用最先进的生物学和遗传学方法也无法回答。
心脏瓣膜病是一个严重的临床问题,影响着5-7%的人口。它的并发症
包括充血性心力衰竭、心内膜炎、房性心律失常和猝死。没有已知的非
外科手术治疗这种疾病的手术疗法。这项拟议的工作利用了以前未被识别的基因数据。
收集自心脏瓣膜病患者;在老鼠身上的研究表明,这类基因是一种重要的
以及以前未被认识的瓣膜结构发育和疾病发病机制的贡献者。这个
这种特殊疾病基因及其调控过程的发现为未来的治疗提供了巨大的潜力。
或对机械稳定的瓣膜组织再生或形成的治疗洞察力将是有益的
给心脏瓣膜病患者。
英文摘要
PROJECT SUMMARY
Based on genetic and cellular discoveries made in the PI lab and his collaborators, this proposal focuses on
novel mechanisms that are critical for formation of heart valves. Data presented in the proposal show that
mutations in the DZIP1 gene cause a very common heart valve disease (i.e., mitral valve prolapse) and can be
caused by errors in how valve tissue forms during development. These discoveries have led to a novel concept
that cilia are involved in valve development. As such, our proposal evaluates how cilia form during development
and how DZIP1 functions to regulate both ciliogenesis and/or β-catenin activities during development. Our
studies will provide unique opportunities to answer questions about heart-valve diseases that heretofore have
been impossible to answer using even state-of-the-art biological and genetic approaches.
Valvular heart disease is a serious clinical problem, affecting 5-7% of the human population. Its complications
include congestive heart failure, endocarditis, atrial arrhythmias, and sudden death. There are no known non-
surgical cures for this group of disease. The proposed work capitalizes on previously unrecognized genetic data
collected from heart valve disease patients; studies in the mouse show that this class of genes is an important
and previously unrecognized contributor to valve structural development and disease pathogenesis. The
uncovering of this particular disease gene and the processes it regulates holds great potential for future remedial
or therapeutic insight towards regeneration or formation of mechanically stable valve tissue that will be beneficial
to valvular heart disease patients.
期刊论文(23)
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DOI:
10.3390/jcdd8050054
发表时间:
2021-05-12
期刊:
Journal of cardiovascular development and disease
影响因子:
2.4
作者:
[Wolters R, Deepe R, Drummond J, Harvey AB, Hiriart E, Lockhart MM, van den Hoff MJB, Norris RA, Wessels A]
通讯作者:
Wessels A
DOI:
10.3390/jcdd9020062
发表时间:
2022-02-17
期刊:
Journal of cardiovascular development and disease
影响因子:
2.4
作者:
[Moore KS, Moore R, Fulmer DB, Guo L, Gensemer C, Stairley R, Glover J, Beck TC, Morningstar JE, Biggs R, Muhkerjee R, Awgulewitsch A, Norris RA]
通讯作者:
Norris RA
DOI:
10.1161/circgen.120.003148
发表时间:
2021-10
期刊:
Circulation. Genomic and precision medicine
影响因子:
--
作者:
[Yu M, Kyryachenko S, Debette S, Amouyel P, Schott JJ, Le Tourneau T, Dina C, Norris RA, Hagège AA, Jeunemaitre X, Bouatia-Naji N]
通讯作者:
Bouatia-Naji N
DOI:
10.3390/jcdd8080098
发表时间:
2021-08-20
期刊:
Journal of cardiovascular development and disease
影响因子:
2.4
作者:
[Goodwin RL, Kheradvar A, Norris RA, Price RL, Potts JD]
通讯作者:
Potts JD
DOI:
10.1002/dvdy.220
发表时间:
2021-03
期刊:
Developmental dynamics : an official publication of the American Association of Anatomists
影响因子:
--
作者:
[Gensemer C, Burks R, Kautz S, Judge DP, Lavallee M, Norris RA]
通讯作者:
Norris RA
共 20 条
Dzip1 and Mitral Valve Prolapse
-
批准号:10171896
-
项目类别:
-
资助金额:$49.93万
-
财政年份:2020
-
负责人:Russell Norris
-
依托单位:
Dzip1 and Mitral Valve Prolapse
-
批准号:10401859
-
项目类别:
-
资助金额:$49.93万
-
财政年份:2020
-
负责人:Russell Norris
-
依托单位:
Cilia and Valvular Heart Disease
-
批准号:10594935
-
项目类别:
-
资助金额:$57.14万
-
财政年份:2016
-
负责人:Russell Norris
-
依托单位:
Cilia and Valvular Heart Disease
-
批准号:10444340
-
项目类别:
-
资助金额:$58.37万
-
财政年份:2016
-
负责人:Russell Norris
-
依托单位:
Cilia and Valvular Heart Disease
-
批准号:10849234
-
项目类别:
-
资助金额:$57.13万
-
财政年份:2016
-
负责人:Russell Norris
-
依托单位:
Cilia and Valvular Heart Disease
-
批准号:9276120
-
项目类别:
-
资助金额:$37.38万
-
财政年份:2016
-
负责人:Russell Norris
-
依托单位:
Developmental and Biomechanical Mechanisms of Valve Tissue Formation
-
批准号:9279166
-
项目类别:
-
资助金额:$9.5万
-
财政年份:--
-
负责人:Russell Norris
-
依托单位:
Developmental and Biomechanical Mechanisms of Valve Tissue Formation
-
批准号:9069880
-
项目类别:
-
资助金额:$20.93万
-
财政年份:--
-
负责人:Russell Norris
-
依托单位:
Developmental and Biomechanical Mechanisms of Valve Tissue Formation
-
批准号:8742737
-
项目类别:
-
资助金额:$22.59万
-
财政年份:--
-
负责人:Russell Norris
-
依托单位:
海外基金