Rat Models for Sex Steroid Action
Rat Models for Sex Steroid Action
批准号:
8518974
负责人:
MICHAEL J SOARES
金额:
$17.95万
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:
2013-05-27 至 2015-04-30
关键词:
AffectAnimal ModelBindingBiological ModelsBiologyBrainCancer BiologyCardiovascular systemChemical IndustryCommunitiesDevelopmentDiagnosticDisciplineDiseaseESR1 geneESR2 geneEndocrineEnvironmental HealthEstradiolEstrogen Receptor alphaEstrogen Receptor betaEstrogensFemaleGenetic TranscriptionGenomeGonadal Steroid HormonesGrowth and Development functionHealthHormonesHumanImmuneImmunologyInvestigationKidneyKnock-outLigandsMalignant NeoplasmsMetabolismMicrotusModelingMusMutant Strains MiceMutant Strains RatsMutationNeuronsNeurosciencesOrganismPharmacologic SubstancePharmacologyPhenotypePhysiological ProcessesPhysiologyPre-Clinical ModelProgesteroneProgesterone ReceptorsProgestinsPubMedPublicationsRattusRegulator GenesRelative (related person)ReproductionResearchResearch PersonnelScienceSignal PathwaySignal TransductionStudy modelsTexasTherapeuticTransgenic OrganismsUniversitiesWomen&aposs HealthZinc Fingersactivating transcription factorbiomedical scientistbody systemcellular targetinggenetic manipulationinsightnucleasenull mutationpre-clinicalpublic health relevancereproductivereproductive axissuccesstherapeutic developmenttool
中文摘要
描述(由申请人提供):适当的动物模型有助于生物医学科学的科学研究。大鼠是用于研究生理过程的有价值的模型,并且是制药和农业化学工业使用的主要临床前动物模型系统。雌激素和孕激素是影响整个生物体生理机能的关键激素。这些激素通过与特定配体激活的转录因子的物理相互作用作用来调节基因转录,从而作用于其细胞靶点。雌激素通过雌激素受体α(ESR1)和雌激素受体β(ESR2)结合并发出信号,而孕酮通过孕酮受体(PGR)发出信号。对性类固醇激素的研究一直是开发用于治疗各种疾病和健康相关病症的疗法的核心。对特定细胞信号通路的参与的研究极大地受益于具有关键调控基因突变的动物模型的可用性。这对于雌激素和孕酮信号通路来说当然是正确的。在Esr1、Esr2和Pgr基因座具有无效突变的小鼠提供了关于雌激素和雌激素调节蛋白作用的生理学的重要见解。然而,小鼠在某些研究领域有局限性,特别是那些与生理学和药理学相关的领域,其中大鼠已被证明是更好的动物模型。在老鼠的遗传操作方面已经取得了相当大的进展。这些包括应用锌指核酸酶(ZFN)基因组编辑来产生大鼠敲除菌株。在这个应用中,我们建议生成和表征性类固醇激素作用的大鼠模型。我们将独立地针对Esr1、Esr2和Pgr 2。我们的突变大鼠品系的表征将集中在与女性生殖道相关的表型。具有雌激素和孕激素信号中断的大鼠将为一系列学科的生物医学科学家提供新的工具,包括癌症生物学,生殖,妇女健康,环境健康,代谢,免疫学,神经科学和心血管生物学。这些新的动物模型将提供给研究界。
英文摘要
DESCRIPTION (provided by applicant): Appropriate animal models facilitate scientific investigation in the biomedical sciences. The rat is a valuable model for studying physiological processes and is the dominant pre-clinical animal model system used by the pharmaceutical and agro-chemical industries. Estrogens and progestins are key hormones affecting the physiology of the entire organism. These hormones act on their cellular targets through physical interactions with specific ligand-activated transcription factors to regulate gene transcription. Estradiol binds and signals through estrogen receptor alpha (ESR1) and estrogen receptor beta (ESR2), while progesterone signals through the progesterone receptor (PGR). Research on sex steroid hormones has been central to the development of therapeutics for the treatment of a variety of diseases and health related conditions. Research on the involvement of specific cell signaling pathways have benefitted tremendously from the availability of animal models possessing mutations in critical regulatory genes. This is certainly true for estrogen and progestin signaling pathways. Mice with null mutations at the Esr1, Esr2, and Pgr loci have provided significant insights about the physiology of estrogen and progestin actions. However, the mouse has limitations for some fields of investigation, especially those related to physiology and pharmacology where the rat has proven to be a much better animal model. Considerable advances have been made in genetic manipulation of the rat. These include the application of zinc finger nuclease (ZFN) genome editing to produce rat knock out strains. In this application, we propose to generate and characterize rat models for sex steroid hormone action. We will independently target Esr1, Esr2, and Pgr2. Our characterization of the mutant rat strains will focus on phenotypes associated with the female reproductive tract. Rats possessing disruptions in estrogen and progesterone signaling will provide new tools for biomedical scientists in a range of disciplines, including cancer biology, reproduction, women's health, environmental health, metabolism, immunology, neurosciences, and cardiovascular biology. These new animal models will be made available to the research community.
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