Integrative Experimental and Theoretical Studies of the Mechanics of Phagocytosis

吞噬作用机制的综合实验和理论研究

• 批准号: 7572896
• 负责人: Volkmar Heinrich
• 金额: $ 33.36万
• 依托单位: UNIVERSITY OF CALIFORNIA AT DAVIS
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-03-15 至 2012-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7572896
• 关键词: Adhesions; Affect; Antibodies; Behavior; Biological Assay; Biological Models; Cells; Cellular Morphology; Characteristics; Coccidioides; Communicable Diseases; Complement; Computer Simulation; Custom; Data Analyses; Dependence; Development; Dictyostelium; Disease; Elements; Exhibits; Experimental Models; Failure; Figs - dietary; Germ Cells; Health; Human; Image; Immune; Immune response; Immunity; Immunofluorescence Immunologic; Individual; Infection; Infectious Agent; Knock-out; Leukocytes; Measurement; Measures; Mechanics; Mediating; Methods; Modeling; Molecular; Molecular Motors; Monitor; Morphology; Motor; Motor Activity; Movement; Mus; Myosin ATPase; Nature; Pathway interactions; Phagocytes; Phagocytosis; Pharmaceutical Preparations; Phenotype; Play; Positioning Attribute; Process; Property; Published Comment; Recovery; Research Personnel; Role; Solid; Stress; Structure; System; Testing; Theoretical Studies; Theoretical model; Time; United States; Validation; Variant; Video Microscopy; Work; base; cell motility; fungus; immune function; macrophage; mechanical behavior; monocyte; nanoscale; neutrophil; pathogen; physical model; programs; research study; response; success; theories; virtual

DESCRIPTION (provided by applicant): The phagocytic neutralization of pathogens plays a central role in host protection against, and recovery from infection. The proposed project aims to expose the major mechanical determinants of phagocytosis by firmly integrating single-cell experiments with advanced theoretical models of "virtual immune cells". This interdisciplinary effort ties closely into the long-term objective of establishing a solid quantitative understanding of autonomous cell motility and its role in the innate immune response. An integrative experimental/theoretical approach will first be used to establish a baseline of key models of phagocytosis (Aim 1) and of different phagocytic pathways (Aim 2). It will then be applied to genetically altered model systems in order to elucidate the mechanical roles of major molecular components for normal phagocytic function (Aim 3). The method's relevance as a valuable single-cell assay in studies of the innate immune function will be validated by examining the phagocytosis of infectious pathogens (Aim 4). The experimental configuration most suitable for close integration with theoretical models consists of an initially spherical cell that engulfs a spherical bead. Single-cell phagocytosis of spherical targets will be monitored using a custom-built videomicroscopy/micropipette-manipulation setup. Data analysis will provide the time courses of cellular morphology, cortical tension, and bead movement for each experiment. These quantitative measurements will serve as standards for the validation of finite-element computer models that are based on physically realistic and biologically plausible rules. The models' success in reproducing the observations will place strong constraints on the forces at play in phagocytosis. The changes in parameter values that are required to accommodate genetically altered or diseased states will noninvasively expose the impact of the affected nanoscale structures on molecular motor activity and cytoskeletal properties. The focus on a standardized single cell/single target configuration that is highly reproducible and simple enough to be quantitatively analyzed presents a unique viewpoint on the phagocytic phenotype. The integration of experiment and theory reveals in detail how the immune phagocytic response fails or succeeds depending on the nature of both phagocyte and pathogen. This is a determining element for the recovery from infectious challenges in human health.

描述（由申请人提供）：病原体的吞噬性中和在宿主保护和从感染中恢复中起着核心作用。拟议的项目旨在通过将单细胞实验与“虚拟免疫细胞”的高级理论模型牢固地整合到单细胞实验中，以揭示吞噬作用的主要机械决定因素。这项跨学科的努力与对自主细胞运动及其在先天免疫反应中的作用建立可靠的定量理解的长期目标紧密相关。首先将使用综合实验/理论方法来建立关键吞噬作用模型的基线（AIM 1）和不同的吞噬途径（AIM 2）。然后，它将应用于遗传改变的模型系统，以阐明主要分子成分在正常吞噬功能方面的机械作用（AIM 3）。该方法作为对先天免疫功能的研究中有价值的单细胞测定法的相关性将通过检查传染病的吞噬作用来验证（AIM 4）。最适合与理论模型紧密整合的实验构型由最初吞噬球形珠的球形细胞组成。球形靶标的单细胞吞噬作用将使用定制的视频显微镜/微孔操作设置来监测。数据分析将为每个实验提供细胞形态，皮质张力和珠子运动的时间过程。这些定量测量结果将作为基于物理上现实且在生物学上合理的规则的有限元计算机模型验证的标准。模型在复制观测方面的成功将对吞噬作用的力量施加强大的限制。适应遗传改变或患病状态所需的参数值的变化将无创地暴露受影响的纳米级结构对分子运动活性和细胞骨架特性的影响。对标准化的单个单元/单个目标配置的关注，该配置高度可重复且简单，以至于对吞噬细胞表型提出了独特的观点。实验和理论的整合详细揭示了免疫吞噬反应如何取决于吞噬细胞和病原体的性质。这是从人类健康中恢复传染性挑战的确定要素。