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miR-181b, endothelial cells, and vascular inflammation

miR-181b、内皮细胞和血管炎症

基本信息

批准号：
10683722
负责人：
MARK W FEINBERG
金额：
$ 63.1万
依托单位：
BRIGHAM AND WOMEN'S HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-08-01 至 2025-07-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10683722
关键词：
ADORA3 gene Adenosine Age Aging Arterial Fatty Streak Atherosclerosis Bioinformatics Biology Bioluminescence Blood Vessels Cardiovascular system Cell Adhesion Molecules Cell Aging Cell Communication Cell physiology Cessation of life Characteristics Chronic Chronic Disease Coronary Arteriosclerosis DNA Damage Development Disease Disease Progression Endothelial Cells Endothelium Foundations Functional disorder Genes Goals Grant Human Hyperlipidemia Inflammation Inflammatory Inflammatory Response Inherited Knockout Mice Lesion Leukocytes Link MADH3 gene MAP Kinase Gene MAPK8 gene Mediating MicroRNAs Molecular Morbidity - disease rate Mus Mutation Myocardial Infarction Nodal Pathway interactions Peripheral Vascular Diseases Phenotype Process Proto-Oncogene Proteins c-akt Regulation Reporter Genes Research Risk Factors Role Signal Pathway Signal Transduction Societies Specimen Stimulus Stroke Therapeutic Tissues Untranslated RNA Untranslated Regions Vascular Cell Adhesion Molecule-1 Vascular Diseases Vascular Endothelium aged atherogenesis cell type chemokine crosslinking and immunoprecipitation sequencing cytokine frontier in vivo inflammatory marker inhibitor insight intravital microscopy molecular imaging mortality multidisciplinary nanomedicine nanoparticle novel novel therapeutic intervention overexpression posttranscriptional promoter response senescence therapeutic miRNA transcriptome sequencing vascular inflammation

项目摘要

Endothelial cell (EC) activation and dysfunction increases with age and is linked to a variety of chronic vascular inflammatory disease states including atherosclerosis—the major cause of morbidity and mortality in Western Societies. Vascular senescence induced by the DNA damage response (DDR) promotes chronic inflammation in atherosclerotic lesions. Senescence-associated proinflammatory cytokines and proatherogenic risk factors (acquired or inherited) such as hyperlipidemia activate key signaling pathways that increase expression of adhesion molecules, chemokines on several cell types, including the vascular endothelium. Therefore, suppressing the senescence-associated inflammatory response in the vascular endothelium may provide a novel therapeutic approach to limit atherosclerosis. MicroRNAs (miRNAs) are small, single-stranded, evolutionary conserved non-coding RNAs that suppress the expression of target genes at the post-transcriptional level and participates in a variety of pathophysiological processes including the regulation of inflammatory responses. Our group provided the initial link implicating miR-181b in suppressing endothelial cell inflammation. During the last grant period, we identified miR-181b as a nodal regulator of endothelial cell quiescence through its regulatory effects on two major signaling pathways – NF-κB and AKT/eNOS. Consequently, endogenous miR-181b was found to function as a key determinant of the inflammatory response in vivo, findings that correlate with human inflammatory states including established coronary artery disease. We now identify endothelial miR-181b as a critical determinant of systemic vascular inflammation and atherosclerosis by controlling vascular senescence and the DNA damage response. Furthermore, we demonstrate that the adenosine-A3AR signaling pathway, a translationally relevant target that suppresses endothelial activation, functions in a miR-181b-dependent manner. These observations provide the foundation for the central hypothesis that endothelial miR-181b, via inhibitory effects on the DNA damage response, regulates senescence-associated vascular inflammation and atherosclerosis. To better understand the precise role of miR-181b in regulating vascular senescence, inflammation, and atherosclerosis, we propose 3 aims. In Aim1, we will determine the molecular basis for miR- 181b to regulate the DNA damage response and vascular senescence in response to diverse stimuli. In Aim2, we will explore the effect of altering miR-181b expression on senescence-associated secretory phenotype and atherosclerotic progression and regression in young and aged mice. In Aim3, we will determine whether the anti-senescent effects of adenosine in the vascular endothelium depend on miR-181b. This multi-disciplinary team in the fields of non-coding RNA biology, molecular imaging, nanomedicine, bioinformatics, and atherosclerosis research will establish an unprecedented molecular view of this miRNA in lesions that can inform a new frontier in the regulation of vascular senescence and atherosclerosis.

内皮细胞（EC）的激活和功能障碍随着年龄的增长而增加，并与各种慢性血管疾病有关。炎症性疾病状态，包括动脉粥样硬化-西方国家发病率和死亡率的主要原因社团。DNA损伤反应（DDR）诱导的血管衰老促进慢性炎症动脉粥样硬化病变。衰老相关的促炎细胞因子和致动脉粥样硬化危险因素（获得性或遗传性），如高脂血症激活关键信号通路，增加粘附分子，趋化因子在几种细胞类型，包括血管内皮。因此，我们认为，抑制血管内皮中衰老相关的炎症反应可以提供限制动脉粥样硬化的新治疗方法。 microRNA（miRNAs）是一类小的、单链的、进化保守的非编码RNA，在转录后水平抑制靶基因的表达，并参与多种病理生理过程，包括炎症反应的调节。我们的团队提供了最初的链接暗示miR-181 b抑制内皮细胞炎症。在上一次拨款期间，我们发现miR-181 b是内皮细胞静止的节点调节因子，通过其对两个细胞的调节作用，主要信号通路- NF-κB和AKT/eNOS。因此，发现内源性miR-181 b 作为体内炎症反应的关键决定因素，与人类相关的发现炎症状态，包括确诊的冠状动脉疾病。我们现在将内皮细胞miR-181 b鉴定为一种通过控制血管衰老来控制全身性血管炎症和动脉粥样硬化的关键决定因素和DNA损伤反应。此外，我们还证明了腺苷-A3 AR信号通路，抑制内皮活化的病理相关靶点，在miR-181 b依赖性方式这些观察结果为核心假设提供了基础，即内皮细胞miR-181 b，通过对DNA损伤反应的抑制作用，调节衰老相关的血管炎症，动脉粥样硬化为了更好地理解miR-181 b在调节血管衰老中的确切作用，炎症和动脉粥样硬化，我们提出3个目标。在Aim 1中，我们将确定miR-1的分子基础。 181 b调节DNA损伤反应和血管衰老对不同刺激的反应。在目标2中，我们将探索改变miR-181 b表达对衰老相关分泌表型的影响，年轻和老年小鼠的动脉粥样硬化进展和消退。在目标3中，我们将确定腺苷在血管内皮中的抗衰老作用依赖于miR-181 b。这种多学科非编码RNA生物学、分子成像、纳米医学、生物信息学和动脉粥样硬化的研究将建立一个前所未有的关于这种miRNA在病变中的分子观点，为血管衰老和动脉粥样硬化的调节提供了新的前沿。