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Investigating the Role of Epigenetic Changes in Early Development and Prevention of Cardiovascular Inflammation

研究表观遗传变化在心血管炎症早期发展和预防中的作用

基本信息

批准号：
10618832
负责人：
Jessie Elizabeth Clark Axsom
金额：
$ 4.77万
依托单位：
UNIVERSITY OF PENNSYLVANIA
依托单位国家：
美国
项目类别：
财政年份：
2021
资助国家：
美国
起止时间：
2021-05-01 至 2024-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10618832
关键词：
ATAC-seq Aerobic Exercise Affect Animals Area Base Sequence Basic Science Bioinformatics Biological Assay Biological Markers Blood Vessels Cardiac Cardiovascular Diseases Cardiovascular system Cause of Death Chromatin Chronic Complication Complications of Diabetes Mellitus Data Development Diagnosis Dietary Intervention Disease Disease Progression Early identification Early treatment Endothelial Cells Ensure Epigenetic Process Exercise Experimental Designs Functional disorder Future Gene Expression Genes Genetic Transcription Genome Glucose Glucose tolerance test Glycosylated Hemoglobin Goals Health Health Promotion Heart Heart Hypertrophy Hemoglobin concentration result High Fat Diet Hyperglycemia Inflammation Inflammatory Insulin Resistance Intervention Length Measures Mediating Metabolic Diseases Methods Modeling Moderate Exercise Modification Morbidity - disease rate Mus Myocardial Infarction Myocardial Ischemia Non-Insulin-Dependent Diabetes Mellitus Nurses Pathway interactions Patients Persons Physicians Prevention Quality of life Randomized Research Risk Role Running Scientist Source Strategic Planning Testing Tissues Translating Translational Research Variant Vascular Diseases Weight Work angiogenesis cell type diet and exercise dietary control disorder prevention exercise intervention exercise physiologist experimental study genetic risk factor glycemic control improved innovation insulin tolerance lifestyle intervention mortality mouse model novel prevent response sedentary whole genome

项目摘要

PROJECT SUMMARY Cardiovascular disease (CVD) kills one person every 37 seconds in the U.S. and those with type 2 diabetes mellitus (T2DM) have a 2-fold higher mortality following a myocardial infarction. The principal cause of T2DM morbidity and mortality is CVD. Genetic risk factors and biomarkers for T2DM have been identified but neither accurately predicts cardiovascular complications. An emerging, novel early prediction method of CVD in T2DM is epigenetics. Epigenetic changes are modifications to the genome that regulate gene transcription without actually changing the underlying nucleotide sequence. Endothelial cells (ECs), which line the interior of blood vessels, become dysfunctional in T2DM and are the first step in CVD progression. ECs maintain long-term expression of pro-inflammatory genes even after normal glucose levels have been attained, suggesting epigenetic changes might be responsible for enduring changes in gene expression that contribute to CVD. It is unknown, however, the extent to which epigenetic changes mediate early cardiac endothelial cell dysfunction in T2DM and whether these changes can be rescued with lifestyle interventions like exercise. The short-term goal of this project is to determine the effect of hyperglycemia on epigenetic modifications (measured via chromatin accessibility) in cardiac endothelial cells and how these are modified by an exercise intervention in a translational mouse model. The long-term goal is to help develop early effective prediction, prevention, and management of cardiovascular complications in patients with T2DM. I hypothesize hyperglycemia will cause differential chromatin accessibility in inflammatory pathway genes that will be prevented by concurrent aerobic exercise. I will test this hypothesis using two specific aims: 1. Determine the effect of hyperglycemia and insulin resistance on epigenetic changes in cardiac endothelial cells. I will use a translational mouse model, which is readily available in our lab, to implement a diet intervention and isolate cardiac endothelial cells. 2. Test whether an aerobic exercise intervention prevents hyperglycemia-induced epigenetic changes in cardiac endothelial cells. I will test four randomly assigned groups of mice: control diet (CD), CD + exercise, high fat diet (HFD), HFD + exercise. This project is significant and innovative because it investigates a long- standing cause of death in an extremely prevalent disease using a novel epigenetic analysis approach. This project fits within the applicant’s long-term research goals of using translational science models to improve understanding, prevention, and treatment of cardiovascular complications in patients with chronic metabolic diseases. This research will establish the early effects of hyperglycemia and insulin resistance on epigenetic changes in cardiac endothelial cells and whether they can be mitigated through exercise, setting the groundwork for effective early identification and treatment of cardiovascular complications in T2DM. The proposed study is aligned with three of the NINR Strategic Plan areas – health promotion and disease prevention, advancing the quality of life, and innovation.

项目摘要心血管疾病（CVD）在美国每37秒就有一人死亡，2型糖尿病患者 2型糖尿病（T2 DM）心肌梗死后的死亡率高2倍。T2 DM的主要病因发病率和死亡率是CVD。已经确定了T2 DM的遗传风险因素和生物标志物，但准确预测心血管并发症。一种新兴的T2 DM CVD早期预测新方法是表观遗传学表观遗传变化是对基因组的修饰，其调节基因转录，而不影响基因表达。实际上改变了潜在的核苷酸序列。内皮细胞（EC），排列在血液内部血管，在T2 DM中变得功能障碍，并且是CVD进展的第一步。EC维持长期即使在达到正常葡萄糖水平后，促炎基因的表达也是如此，这表明表观遗传变化可能是导致CVD的基因表达持续变化的原因。是然而，尚不清楚表观遗传变化在多大程度上介导了早期心脏内皮细胞功能障碍以及这些变化是否可以通过运动等生活方式干预来挽救。短期本项目的目的是确定高血糖对表观遗传修饰的影响（通过染色质可及性），以及这些是如何通过运动干预改变的。小鼠平移模型。长期目标是帮助发展早期有效的预测、预防和 T2 DM患者心血管并发症的管理。我假设高血糖会导致炎症途径基因中的差异染色质可及性，有氧运动我将用两个具体目标来检验这个假设：1。确定高血糖的影响和胰岛素抵抗对心脏内皮细胞表观遗传变化的影响。我将使用平移鼠标模型，这是现成的，在我们的实验室，以实施饮食干预和分离心脏内皮细胞细胞2.测试有氧运动干预是否可以预防高血糖诱导的表观遗传变化，心脏内皮细胞我将测试四组随机分配的小鼠：对照饮食（CD），CD +运动，高脂饮食（HFD），HFD +运动。这个项目是重要的和创新的，因为它调查了一个长期的- 使用一种新的表观遗传学分析方法，在一种极其普遍的疾病中确定死亡原因。这项目符合申请人的长期研究目标，即利用转化科学模型来提高了解、预防和治疗慢性代谢性疾病患者的心血管并发症疾病这项研究将确定高血糖和胰岛素抵抗对糖尿病的早期影响。心脏内皮细胞的表观遗传变化以及它们是否可以通过运动来减轻，为心血管并发症的早期有效识别和治疗奠定基础 2型糖尿病拟议的研究与NINR战略计划的三个领域-健康促进和疾病预防、提高生活质量和创新。