Fibronectin alternative splicing in thrombosis and inflammation

纤连蛋白选择性剪接在血栓形成和炎症中的作用

• 批准号: 9199422
• 负责人: Anil Kumar Chauhan
• 金额: $ 37.75万
• 依托单位: UNIVERSITY OF IOWA
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-01-01 至 2018-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9199422
• 关键词: Acute; Alteplase; Alternative Splicing; Apolipoprotein E; Arteries; Atherosclerosis; Blood Circulation; Blood Platelets; Blood Vessels; Blood flow; Bone Marrow; Brain Injuries; Carotid Artery Thrombosis; Cell Adhesion Molecules; Cells; Cerebrum; Chimera organism; Clinical; Coagulation Process; Diabetes Mellitus; Diagnosis; Disease; Endothelial Cells; Endothelium; Exons; Experimental Animal Model; Fab Immunoglobulins; Fibrinolysis; Fibronectins; Functional disorder; Future; Genes; Goals; Health; Health Care Costs; Human; Hypertension; Infarction; Inflammation; Inflammatory; Injury; Integrins; Ischemia; Ischemic Penumbra; Ischemic Stroke; Knockout Mice; Lead; Life; Ligands; Liver; LoxP-flanked allele; Measures; Mediating; Modeling; Monoclonal Antibodies; Mouse Strains; Mus; Neurological outcome; Neutrophil Infiltration; Outcome; Pathologic; Pathway interactions; Patients; Pilot Projects; Plasma; Platelet aggregation; Process; Reagent; Reperfusion Injury; Reperfusion Therapy; Research Personnel; Risk Factors; Role; Signal Pathway; Signal Transduction; Source; Stroke; TLR4 gene; Testing; Thrombosis; Thrombus; Time; Translating; United States; Variant; Work; acute stroke; clinically significant; common treatment; defined contribution; effective therapy; endothelial dysfunction; high risk; hypercholesterolemia; improved; improved outcome; in vivo; inflammatory marker; insight; intravital microscopy; knowledge of results; macrophage; mouse model; mutant; neuron loss; neutrophil; novel; novel therapeutic intervention; novel therapeutics; overexpression; pre-clinical; prevent; public health relevance; restoration; tegrin; translational approach

DESCRIPTION (provided by applicant): Identifying novel endogenous ligands that promote thrombosis and inflammatory processes in pathological settings, such as, diabetes, hypercholesterolemia and vascular hypertension may lead to new therapies that improve outcomes in patients at high risk for stroke. A variant of fibronectin (FN) containing the alternatively-spliced extra domain A (EDA+-FN), which is absent in the arteries or circulation of healthy humans and mice, is specifically expressed in the endothelium of atherosclerotic arteries and elevated in circulation during pathological settings, such as diabetes, atherosclerosis and vascular hypertension, most likely due to endothelial dysfunction. Recently, we have discovered that EDA+-FN promotes thrombosis and inflammatory processes. The underlying mechanisms by which EDA+-FN contributes to thrombosis and inflammation are not well understood. EDA+-FN is known to activate the toll-like- receptor 4 (TLR4) signaling pathway. Additionally, EDA is a ligand for integrin �9�1, which is expressed on inflammatory cells, such as, neutrophils and macrophages. Hypercholesterolemia is one of the major risk factors for acute stroke in humans. Therefore, in hypercholesterolemic apolipoprotein E-deficient (ApoE-/-, atherosclerosis prone) mice, we propose to test the central hypothesis that EDA+-FN contributes to ischemia/reperfusion (I/R) brain injury in pathological setting, and that it does so by enhancing thrombosis and inflammatory processes via parallel �9�1and TLR4-mediated pathways. In Aim1, we will define the role of TLR4 in EDA+-FN-mediated thrombosis and inflammatory I/R brain injury. In Aim 2, we will determine the role of integrin �9�1 in EDA+-FN -mediated thrombosis and inflammatory I/R brain injury. In Aim 3, we will define the role of plasma versus endothelial cell EDA+-FN in I/R brain injury. Furthermore, we will determine the source of EDA+-FN in the plasma of the aforementioned pathological conditions. As a translational approach, we will test the hypothesis that blocking EDA+-FN with specific monoclonal antibodies will reduce stroke injury in the context of hypercholesterolemia. To achieve our specific experimental goals, we have developed novel genetically modified mice strains and reagents that we will share with other researchers in the field. The contribution of th proposed studies is highly clinically significant as it determine the mechanistic insights by which EDA+-FN promotes thrombosis and inflammatory brain injury in disease context of atherosclerosis. The proposal has future translational potential, as it may have significant impact on the diagnosis and treatment of common thrombo-inflammatory diseases including acute stroke.

描述（申请人证明）：识别促进和炎症过程的新型内源配体，因为糖尿病，高胆固醇和血管高血压可能会导致新的，该新的含量为OK的变种。在动脉粥样硬化动脉的内皮中表达的额外域A（EDA+-FN）在病理环境中的循环中升高，例如糖尿病，动脉粥样硬化和血管高血压，这很可能是由于吸收性的。 EDA+-FN有助于血栓形成，而EDA+-FN则可以激活Toll-tlike-the-tlr4（TLR4）信号通路，EDA是整合素的配体，例如中性粒细胞和巨噬细胞人类急性中风的危险因素。 通过增强了炎症性弯曲式的9.1和TLR4介导的途径，在AIM1 DA+-FN介导的血栓形成和炎症I/R脑损伤中。 -FN在I/R脑损伤中。目标，我们已经开发了新型的修饰小鼠菌株和试剂，我们将共享wither carchers eLD的贡献。 EDA+-FN在动脉粥样硬化的情况下促进血栓形成和炎症的脑损伤。 关于包括急性中风在内的Commbo炎症性疾病的诊断和治疗。

项目成果

Endothelial Cell-Derived von Willebrand Factor Is the Major Determinant That Mediates von Willebrand Factor-Dependent Acute Ischemic Stroke by Promoting Postischemic Thrombo-Inflammation.

• DOI: 10.1161/atvbaha.116.307660
• 发表时间: 2016-09
• 期刊: Arteriosclerosis, thrombosis, and vascular biology
• 作者: Dhanesha N;Prakash P;Doddapattar P;Khanna I;Pollpeter MJ;Nayak MK;Staber JM;Chauhan AK
• 通讯作者: Chauhan AK

Endothelial Cell-Derived Von Willebrand Factor, But Not Platelet-Derived, Promotes Atherosclerosis in Apolipoprotein E-Deficient Mice.

• DOI: 10.1161/atvbaha.117.309918
• 发表时间: 2018-03
• 期刊: Arteriosclerosis, thrombosis, and vascular biology
• 作者: Doddapattar P;Dhanesha N;Chorawala MR;Tinsman C;Jain M;Nayak MK;Staber JM;Chauhan AK
• 通讯作者: Chauhan AK

P-selectin can promote thrombus propagation independently of both von Willebrand factor and thrombospondin-1 in mice.

在小鼠中，P-选择素可以独立于冯维勒布兰德因子和血小板反应蛋白-1 促进血栓传播。

• DOI: 10.1111/jth.13586
• 发表时间: 2017
• 期刊: Journal of thrombosis and haemostasis : JTH
• 作者: Prakash,P;Nayak,MK;Chauhan,AK
• 通讯作者: Chauhan,AK

Degradation of platelet-von Willebrand factor complexes by plasmin: an alternative/backup mechanism to ADAMTS13.

纤溶酶降解血小板-血管性血友病因子复合物：ADAMTS13 的替代/备用机制。

• DOI: 10.1161/circulationaha.114.008298
• 发表时间: 2014
• 期刊: Circulation
• 影响因子: 37.8
• 作者: Chauhan,AnilK

Thrombospondin 1 requires von Willebrand factor to modulate arterial thrombosis in mice.

血小板反应蛋白 1 需要冯维勒布兰德因子来调节小鼠动脉血栓形成。

• DOI: 10.1182/blood-2014-06-581942
• 发表时间: 2015
• 期刊: Blood
• 影响因子: 20.3
• 作者: Prakash,Prem;Kulkarni,PareshP;Chauhan,AnilK
• 通讯作者: Chauhan,AnilK