Novel Mechanisms of Quinone Toxicity

醌毒性的新机制

基本信息

批准号：
7880308
负责人：
DAVID ROSS
金额：
$ 34.15万
依托单位：
UNIVERSITY OF COLORADO DENVER
依托单位国家：
美国
项目类别：
财政年份：
2010
资助国家：
美国
起止时间：
2010-06-04 至 2015-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7880308
关键词：
Adverse effects Affect Affinity Chromatography Aftercare Alleles Autophagocytosis Benzoquinones Biological Models Breast Cells Chemicals Data Disease Dopamine Electrons Endoplasmic Reticulum Enzymes Event Frequencies General Population Generations Genetic Genetic Polymorphism High Prevalence Hydroquinones Individual Knock-in Mouse Modeling Molecular Chaperones NADPH-Ferrihemoprotein Reductase NQO1 gene NRH - quinone oxidoreductase2 Naphthoquinones Nature Neurons Oxidation-Reduction Oxidative Stress Oxidoreductase Oxygen Pancreas Pharmacogenetics Predisposition Process Production Proteins Quinone Reductases Quinones Reaction Reactive Oxygen Species Role System Toxic effect Variant Xenobiotics adduct aminochrome 1 biological adaptation to stress body system cell type cytochrome b5 reductase design endoplasmic reticulum stress enzyme activity hydroquinone multicatalytic endopeptidase complex novel p-Benzoquinones protein protein interaction public health relevance relating to nervous system research study response suicide inhibitor

项目摘要

DESCRIPTION (provided by applicant): Both benzoquinones and naphthoquinones have been found to perturb protein handling and degradation in a variety of cellular systems. Protein handling and degradation is not restricted to the proteasome and also involves protein chaperones, the unfolded protein response (UPR)/endoplasmic reticulum (ER) stress response, formation of aggresomes and lysosomal autophagy. Quinones have been found to affect each of these systems and altered protein handling is emerging as a potentially key mechanism of quinone induced toxicity. Our studies will focus on model 1,4-benzo- and naphtho-quinones as well as the dopamine derived 1,2-quinone, aminochrome which have all been shown to induce changes in protein handling. In aim 1, we will characterize changes in all major protein handling systems induced by model benzo- and naphtho- quinones and by aminochrome. These experiments will characterize altered mechanisms of protein handling as a result of treatment of cells with reactive quinones and the relevance of such changes for toxicity in cellular systems. In aim 2, we will define the respective roles of arylation and quinone-induced oxidative stress in inhibited protein handling using quinones capable only of either redox cycling or of both redox cycling and arylation . We will also examine quinone induced changes in protein handling in cells stably transfected with the one electron reductases cytochrome P450 reductase or cytochrome b5 reductase which cause increased quinone one electron redox cycling and increased reactive oxygen generation. The major mammalian quinone reductases NQO1 and NQO2 are highly polymorphic with a high prevalence of variant alleles resulting in marked phenotypic changes. A lack or variation in activity of these enzymes may therefore represent susceptibility factors for quinone induced toxicity. In aim 3, we will examine the role of NQO1 and NQO2 in modulating quinone induced protein handling changes and toxicity. These experiments will be performed in isogenic pancreatic, breast and neural cellular systems specifically designed to explore the roles of NQO1 and NQO2 in the same genetic background Overall, these experiments will characterize novel mechanisms of quinone-induced toxicity at the level of protein handling, define the inter-relationships and the respective roles of protein handling changes in toxicity and define the role of NQO1 and NQO2 as susceptibility factors for these changes. The studies will have broad mechanistic applicability to a variety of organ systems. PUBLIC HEALTH RELEVANCE: The focus of this application is to elucidate novel mechanisms of toxicity of xenobiotic and endogenous quinones at the level of protein handling. The role of both arylation and oxidative stress in quinone-induced alterations in protein handling and toxicity will be defined. The pharmacogenetics of quinone reductases has been characterized and they are highly polymorphic and may represent susceptibility factors for quinone induced toxicity. The studies will have broad applicability to a variety of organ systems.

描述（由申请人提供）：已发现苯醌和萘醌都会干扰多种细胞系统中的蛋白质处理和降解。蛋白质处理和降解不仅限于蛋白酶体，还涉及蛋白质伴侣、未折叠蛋白反应 (UPR)/内质网 (ER) 应激反应、聚集体的形成和溶酶体自噬。已发现醌会影响这些系统中的每一个，并且蛋白质处理的改变正在成为醌诱导毒性的潜在关键机制。我们的研究将集中于模型 1,4-苯并醌和萘醌以及多巴胺衍生的 1,2-醌、氨基色素，这些物质均已被证明可诱导蛋白质处理的变化。在目标 1 中，我们将描述苯醌模型、萘醌模型以及氨基色素引起的所有主要蛋白质处理系统的变化。这些实验将表征由于用反应性醌处理细胞而导致的蛋白质处理机制的改变，以及这种变化与细胞系统毒性的相关性。在目标 2 中，我们将使用仅能够进行氧化还原循环或同时进行氧化还原循环和芳基化的醌来定义芳基化和醌诱导的氧化应激在抑制蛋白质处理中各自的作用。我们还将检查用单电子还原酶细胞色素 P450 还原酶或细胞色素 b5 还原酶稳定转染的细胞中醌诱导的蛋白质处理变化，这会导致醌一电子氧化还原循环增加和活性氧生成增加。主要的哺乳动物醌还原酶 NQO1 和 NQO2 具有高度多态性，变异等位基因的发生率很高，导致显着的表型变化。因此，这些酶活性的缺乏或变化可能代表醌诱导毒性的易感因素。在目标 3 中，我们将研究 NQO1 和 NQO2 在调节醌诱导的蛋白质处理变化和毒性中的作用。这些实验将在专门设计的同基因胰腺、乳腺和神经细胞系统中进行，以探索 NQO1 和 NQO2 在相同遗传背景中的作用。总体而言，这些实验将在蛋白质处理水平上表征醌诱导毒性的新机制，定义蛋白质处理毒性变化的相互关系和各自的作用，并将 NQO1 和 NQO2 的作用定义为这些变化的易感因素。这些研究将对各种器官系统具有广泛的机械适用性。公共健康相关性：本申请的重点是阐明外源性和内源性醌在蛋白质处理水平上的新毒性机制。将定义芳基化和氧化应激在醌诱导的蛋白质处理和毒性改变中的作用。醌还原酶的药物遗传学已得到表征，它们具有高度多态性，可能代表醌诱导毒性的易感因素。这些研究将广泛适用于各种器官系统。