KLF2 as a regulator of endothelial cell biology

KLF2 作为内皮细胞生物学的调节剂

• 批准号: 7460229
• 负责人: MUKESH Kumar JAIN
• 金额: $ 39.25万
• 依托单位: CASE WESTERN RESERVE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-08-01 至 2013-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7460229
• 关键词: Adhesives; Anti-Inflammatory Agents; Anti-inflammatory; Binding; Biochemical; Biological; Biomechanics; Blood Clot; Blood Vessels; Blood coagulation; Cell Line; Cellular biology; Coenzyme A; Disease; Endothelial Cells; Endothelium; Event; Exposure to; Family; Foundations; Functional disorder; Funding; Gene Expression; Gene Targeting; Genetic; Grant; Growth Factor; Health; Homeostasis; Hydroxyl Radical; In Vitro; Inflammatory; Investigation; Mediating; Mediator of activation protein; Medical; Molecular; Morbidity - disease rate; Oxidoreductase; Pathogenesis; Pathway interactions; Pharmaceutical Preparations; Phenotype; Plasminogen Activator Inhibitor 1; Property; Regulation; Research; Role; Societies; Stimulus; Thrombomodulin; Thromboplastin; Thrombosis; Time; Vascular Endothelial Cell; Vascular Endothelium; atherothrombosis; base; cardiovascular disorder therapy; cytokine; human NOS3 protein; in vivo; inhibitor/antagonist; insight; member; mortality; novel; novel therapeutics; overexpression; promoter; shear stress; transcription factor; treatment strategy

DESCRIPTION (provided by applicant): The vascular endothelium produces numerous growth factors, cytokines, and bioactive mediators that critically regulate vascular homeostasis in health and disease. During the previous funding period, we provided evidence that expression of the transcription factor KLF2 in endothelial cells is induced by biomechanical stimuli such as laminar shear stress (LSS) and pharmacologic stimuli such as 3- hydroxyl-3-methyglutaryl coenzyme A reductase inhibitors (also known as statins). We also demonstrated that this induction of KLF2 by both stimuli was dependent on members of the MEF2 family of transcription factors. Studies aimed at elucidating KLF2 function in endothelial cell biology indicate that this factor directly regulates the expression of potent anti-inflammatory and anti-thrombotic factors such as thrombomodulin (TM) and endothelial nitric oxide synthase (eNOS). Importantly, evidence was also provided that the ability of laminar flow or statins to induce TM and eNOS was KLF2 dependent. Finally, our studies demonstrated that KLF2 can inhibit cytokine-mediated induction of pro- inflammatory and pro-thrombotic factors (e.g. tissue factor and plasminogen activator inhibitor-1) through its ability to reduce NFkB activity. Consistent with this effect, KLF2 overexpression increased blood-clotting time while knockdown of KLF2 reduced blood-clotting time. Taken together, these studies provide the basis for this renewal application that will explore the role of KLF2 in greater detail. In Aim 1, we will explore the molecular basis for flow and statin-mediated induction of KLF2 in vitro and in vivo. In Aim 2, we will determine the molecular basis of KLF2 mediated-induction of target genes and the functional consequences of KLF2 deficiency on vascular thrombosis in vivo. And finally, in Aim 3, we will determine the molecular basis of KLF2 mediated-inhibition of proinflammatory target genes and the functional consequences of KLF2-deficiency on atherothrombosis in vivo. We anticipate that these studies will provide novel and fundamental insights regarding the role of KLF2 in endothelial cell biology. Furthermore, a greater understanding of KLF2 function in the context of statins may provide the foundation for novel therapeutic strategies aimed at the treatment of vascular inflammatory and thrombotic disease states. Project Narrative: Despite maximal medical therapy, cardiovascular disease remains the number one cause of morbidity and mortality in our society. As such the identification of novel treatment strategies is clearly required. Current paradigms suggest that dysfunction of the vascular endothelial cell that lines all blood vessels is a critical early event in the pathogenesis of blood vessel diseases. Our studies have identified a genetic factor that can confer favorable properties to endothelial cells and is induced by a class of medications termed statins. Our efforts are focused on developing a greater understanding of this factors role in endothelial cells with the hope that such investigations may provide the foundation for novel therapeutic strategies aimed at the treatment of vascular inflammatory disease states.

描述(申请人提供)：血管内皮细胞产生大量的生长因子、细胞因子和生物活性介质，对健康和疾病中的血管动态平衡起关键调节作用。在之前的资助期间，我们提供了证据表明，转录因子KLF2在内皮细胞中的表达是由生物力学刺激(如层流切应力)和药物刺激(如3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂(也称为他汀类药物))诱导的。我们还证明了这两种刺激对KLF2的诱导依赖于MEF2转录因子家族的成员。旨在阐明KLF2在内皮细胞生物学中作用的研究表明，KLF2直接调节强大的抗炎和抗血栓因子的表达，如血栓调节蛋白(TM)和内皮型一氧化氮合酶(ENOS)。重要的是，也有证据表明层流或他汀类药物诱导TM和eNOS的能力依赖于KLF2。最后，我们的研究表明，KLF2可以通过降低NFkB的活性来抑制细胞因子介导的促炎和促血栓形成因子(如组织因子和纤溶酶原激活物抑制物-1)的诱导。与这一效应一致的是，KLF2过表达增加了凝血时间，而KLF2基因敲除则减少了凝血时间。综上所述，这些研究为这一更新申请提供了基础，将更详细地探索KLF2的作用。在目标1中，我们将探索KLF2在体内外流动和他汀类药物诱导的分子基础。在目标2中，我们将确定KLF2介导的靶基因诱导的分子基础以及KLF2缺乏在体内对血管血栓形成的功能后果。最后，在目标3中，我们将确定KLF2介导的分子基础--抑制促炎靶基因以及KLF2缺乏在体内对动脉粥样硬化血栓形成的功能后果。我们预计这些研究将为KLF2在内皮细胞生物学中的作用提供新的和基本的见解。此外，在他汀类药物的背景下更好地了解KLF2的功能可能会为旨在治疗血管炎症和血栓性疾病状态的新的治疗策略提供基础。 项目简介：尽管进行了最大限度的药物治疗，心血管疾病仍然是我们社会发病率和死亡率的头号原因。因此，确定新的治疗策略显然是必要的。目前的研究范式表明，排列在所有血管中的血管内皮细胞功能障碍是血管疾病发病机制中的一个关键早期事件。我们的研究已经确定了一种遗传因素，它可以赋予内皮细胞良好的特性，并且是由一种名为他汀类药物的药物诱导的。我们的努力集中于更好地了解这一因素在内皮细胞中的作用，希望这些研究可以为旨在治疗血管炎症疾病状态的新的治疗策略提供基础。