Bridging the Gap from Hemodynamic Stress to Intracranial Aneurysm Instability: An Integrated Multimodal Approach

弥合血流动力学应激与颅内动脉瘤不稳定之间的差距：综合多模式方法

• 批准号: 10186321
• 负责人: Naoki Kaneko
• 金额: $ 53.03万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-07-01 至 2026-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10186321
• 关键词: 3-Dimensional; 3D Print; Abnormal Endothelial Cell; Address; Affect; Aneurysm; Angiography; Animal Model; Area; Biological; Biological Markers; Bulla; Cell Shape; Cellular Morphology; Characteristics; Clinical; Collaborations; Complex; Data; Data Set; Databases; Development; Diagnostic Imaging; Diagnostic radiologic examination; Endothelial Cells; Endothelium; Exhibits; Functional disorder; Gene Expression; Goals; Growth; Harvest; Human; Image; In Vitro; Inflammation; Intracranial Aneurysm; Investigation; Knowledge; Lead; Link; Liquid substance; Maps; Mediating; Medical; Methods; Microscopic; Microscopy; Modeling; Molecular; Monitor; Morbidity - disease rate; Operative Surgical Procedures; Pathologic; Patients; Permeability; Pharmacology; Pharmacotherapy; Prevention; Regulation; Reporting; Research; Risk; Risk Factors; Role; Rotation; Rupture; Ruptured Aneurysm; Sampling; Scanning; Signal Pathway; Signal Transduction; Source; Spatial Distribution; Stress; Subarachnoid Hemorrhage; System; Techniques; Technology; Testing; Thinness; Time; Tissue Sample; Tissues; To specify; Unnecessary Surgery; Vascular Endothelial Cell; base; cerebrovascular; clinical database; clinical imaging; data integration; follow-up; hemodynamics; high risk; histological image; human imaging; in vitro Model; innovation; microCT; mortality; multidisciplinary; multimodality; multiphoton microscopy; novel; precision medicine; response; risk prediction; simulation; stressor; tool

1 Project Summary 2 3 The overall goal of this project is to develop accurate and reliable prediction tools and pharmacological targets 4 for the prevention of rupture of intracranial aneurysms (IAs). Abnormal hemodynamic stress such as 5 impingement flow with high wall shear and oscillating flow with low wall shear, is intimately linked with the growth 6 and rupture of IAs. However, detailed mechanisms underlying weak IA walls are not yet defined due to (1) the 7 absence of technologies for profiling the spatial distribution of gene expression of endothelial cells (ECs) induced 8 by the complex hemodynamic flow stressors created in IAs, (2) difficulties in collecting sequential clinical images 9 of growing IAs and acquiring human IA tissue samples to validate biologic mechanisms, and (3) the absence of 10 technologies allowing integration of the data from 3D multimodal techniques. To overcome these obstacles, we 11 have built a strong, multidisciplinary team and created a new experimental system that bridges human samples, 12 imaging, and dynamic modeling platforms. In this project, we challenge two fundamental questions regarding 13 hemodynamic stress and induced responses within the IAs. First, does complex abnormal hemodynamic stress 14 within human IAs induce abnormal regulation of EC signaling pathways? Second, what signaling pathways in 15 EC link unstable wall remodeling during IA growth and rupture? To address these questions, we have pioneered 16 a 3D Live EC Aneurysmal Flow Simulator (3D LEAFS) for profiling the spatial distribution of EC responses to 17 complex hemodynamic flow stress created in patient-specific IAs. Preliminary studies demonstrate that abnormal 18 flow in IAs induces abnormal EC morphology, cellular dysfunction and inflammation, and increased permeability. 19 We have developed an extensive database of clinical images of growing IAs and also tissue samples, exploiting 20 integrated flow analysis and 3D histological imaging of human IA tissue scanned with micro-CT and multiphoton 21 microscopy. With this database, we have linked abnormal flow with IAs to growth, wall thinning and weak wall 22 remodeling leading to rupture. By combining these state-of-the-art technologies, we propose to examine 23 fundamental impact of abnormal flow stress on ECs, and identify relationships between EC pathophysiological 24 responses and wall changes leading to fragile walls, growth and rupture. The proposed research is innovative 25 because this will be the first research to answer the above questions by utilizing multimodalities including 26 longitudinal follow-up images, surgical video, micro-CT, multiphoton microscopy, in vitro 3D endothelialized flow 27 simulator, and flow analysis for development of a pipeline for linking flow-induced EC responses to pathologic 28 changes in human IA tissue. The specific aims of this project are: 1) determine the EC signaling pathways 29 associated with unstable wall remodeling, 2) correlate pathological EC responses with IA growth, and 3) 30 determine the EC responses evoked by several characteristic abnormal hemodynamic flow conditions. The 31 proposed research will enhance development of precision medicine strategies that leverage diagnostic imaging 32 with risk prediction and translational therapies.

1项目概述