Transgenic Models of Ah Receptor Action

Ah 受体作用的转基因模型

• 批准号: 8411128
• 负责人: CHRISTOPHER A BRADFIELD
• 金额: $ 33.19万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-01-10 至 2016-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8411128
• 关键词: ARNT gene; Acute; Affinity; Agonist; Alleles; Animal Model; Aromatic Polycyclic Hydrocarbons; Aryl Hydrocarbon Receptor; Biological; Biological Markers; Candidate Disease Gene; Cells; Chemical Structure; Complex; Coupled; DNA; Data Set; Dependence; Development; Developmental Biology; Dioxins; Endothelial Cells; Environment; Environmental Health; Environmental Pollution; Exposure to; Gene Expression; Gene Targeting; Genetic Enhancer Element; Genetic Polymorphism; Genomics; Goals; Grant; Health Policy; Hepatocyte; Human; Individual; Ligands; Liver neoplasms; Mediating; Modeling; Mus; Outcome; Pathway interactions; Physiological; Play; Polychlorinated Biphenyls; Population; Receptor Signaling; Recombinants; Risk; Risk Assessment; Rodent; Role; Signal Pathway; Signal Transduction; Staging; Testing; Toxic effect; Toxicity Tests; Toxicology; Transcript; Transcriptional Activation; Transgenic Model; Tumor Promotion; activating transcription factor; aryl hydrocarbon receptor ligand; base; carcinogenesis; dibenzofuran; diphenyl; embryonic stem cell; environmental chemical; hazard; insight; man; mouse model; mutant; novel; pollutant; receptor; research study; response

DESCRIPTION (provided by applicant): The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor that mediates the biological effects of polycyclic aromatic hydrocarbons (PAHs), halogenated-dioxins ("dioxins"), - dibenzofurans, -biphenyls (PCBs), and -diphenylethers. Because of its central role in acute toxicity, teratogenesis and carcinogenesis of a large number of environmental contaminants, mechanistic information about AHR signaling is used by regulatory agencies to establish acceptable exposure levels for these pollutants. The overarching hypothesis of this proposal is that at least three distinct AHR signaling pathways exist that are of toxicological significance to human populations and vertebrate species in general. We propose that these three pathways can be distinguished by their unique impacts on transcriptional profiles within target cell populations and that these pathways can be further defined based upon their dependence on fractional activation of the AHR, by their cellular context, and their influence on gene expression through enhancer elements known as AHREs. The goal of this proposal is to identify biomarkers that reflect exposure to agonists and their induced toxic responses. We will accomplish this through the identification of low and high affinity AHREs in the hepatocyte and endothelial cell compartments of novel recombinant mouse models. To these ends, we propose the following specific aims: Specific Aim 1: Use gene targeting in ES cells to generate recombinant alleles derived from a ligand responsive version of Ahr. Specific Aim 2: Demonstrate the importance of the cellular expression and concentration of AHR. Specific Aim 3: Classify the high and low affinity AHRE batteries using genomic approaches. Specific Aim 4: Provide evidence that environmental AHR agonists can stimulate the endogenous AHR pathway. We propose that the results of this effort will provide new models that will inform the mechanism of dioxin toxicity in humans, characterize DNA signatures of toxicity, and test a novel hypothesis that developmental toxicity arises from interference with the endogenous AHR pathway. Collectively these studies will set the stage for more accurate and informative risk assessment in man.

描述（由申请人提供）：芳烃受体（AHR）是一种配体激活的转录因子，介导多环芳烃（PAH）、卤代二恶英（“二恶英”）、-二苯并呋喃、-联苯（PCB）和-二苯醚的生物效应。由于其在大量环境污染物的急性毒性、致畸作用和致癌作用中的核心作用，有关AHR信号传导的机制信息被监管机构用于确定这些污染物的可接受暴露水平。该建议的总体假设是，至少存在三种不同的AHR信号通路，它们对人类种群和脊椎动物物种具有毒理学意义。我们建议，这三种途径可以区分其独特的影响，在靶细胞群内的转录谱，这些途径可以进一步定义的基础上，他们的依赖于分数激活的AHR，他们的细胞环境，和他们的影响，通过增强子元件被称为AHRE的基因表达。该提案的目标是确定反映暴露于激动剂及其诱导的毒性反应的生物标志物。我们将通过在新型重组小鼠模型的肝细胞和内皮细胞隔室中鉴定低亲和力和高亲和力AHRE来实现这一点。为此，我们提出了以下具体目标：具体目标1：在ES细胞中使用基因靶向来产生源自Ahr的配体响应版本的重组等位基因。具体目标2：证明AHR的细胞表达和浓度的重要性。具体目标3：使用基因组方法对高亲和力和低亲和力AHRE电池进行分类。具体目标4：提供环境AHR激动剂可刺激内源性AHR通路的证据。我们建议，这一努力的结果将提供新的模型，将告知二恶英在人类中的毒性机制，表征DNA签名的毒性，并测试一个新的假设，即发育毒性产生的干扰与内源性AHR途径。总的来说，这些研究将为人类更准确和信息丰富的风险评估奠定基础。