Mechanical Regulation of Actin Networks

肌动蛋白网络的机械调节

• 批准号: 8099618
• 负责人: DANIEL A FLETCHER
• 金额: $ 21.64万
• 依托单位: UNIVERSITY OF CALIFORNIA BERKELEY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-04-01 至 2012-09-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8099618
• 关键词: Actin-Binding Protein; Actins; Affect; Behavior; Biochemical; Biological; Cell division; Cells; Complement; Complex; Computer Architectures; Development; Disease; Endocytosis; Exocytosis; Extracellular Matrix; Filament; Fluorescence Microscopy; Growth; Health; Individual; Intercellular Junctions; Measurement; Measures; Mechanics; Microfilaments; Modeling; Movement; Neoplasm Metastasis; Phagocytosis; Physical environment; Play; Process; Property; Proteins; Recording of previous events; Regulation; Role; Scanning Probe Microscopes; Shapes; Signal Transduction; System; T-Lymphocyte; Techniques; Time; Tissues; Up-Regulation; Work; base; cantilever; cell motility; cofilin; crosslink; density; drug discovery; in vitro Model; insight; mechanical behavior; neutrophil; pathogen; profilin; research study; response; tool

DESCRIPTION (provided by applicant): Crawling cells in the body must traverse a complex landscape obstructed by cell-cell junctions, extracellular matrix, and other cells. The elegant and apparently effortless navigation of neutrophils through tissue in tension at one moment and in compression the next raises questions about how motile cells respond to external as well as self-imposed loads. More specifically, how are the actin filament networks that generate cellular protrusions during motility influenced by the forces on them? The common view of dynamic actin networks as having properties governed only by concentrations of actin and binding proteins is not sufficient to explain how cells adapt to their physical environment; the role of forces in restructuring or remodeling actin networks must be considered. We hypothesize that external loads mechanically regulate actin network properties by altering network architecture, such as filament density and crosslinking, in response to changes in loading conditions. This `tuning' or adaptation of actin network mechanical properties and growth rates in response to load may be an important mechanism for guiding crawling cells and play critical roles in other actin-based processes including endocytosis, phagocytosis, and mechanotransduction. However, basic questions about the physical behavior of dynamic actin networks remain unanswered. This proposal focuses on the response of Arp2/3-branched actin networks to forces. Using an in vitro model of actin network growth, we ask several basic questions about mechanical properties, growth rates, and the role of actin binding proteins in organizing network architecture. We have developed a dual-cantilever atomic force microscope (AFM) with time-lapse fluorescence microscopy that has the unique ability to measure both static and dynamic actin network properties under controlled loading conditions. In preliminary experiments using this technique, we have identified complex mechanical behavior of actin networks under high loads and growth rates that depend on loading history rather than instantaneous load. This proposal will use a minimal system of purified proteins that form growing actin networks to (i) identify the effect of loading on mechanical properties, (ii) track changes in growth rates in response to force, and (iii) examine the transient effect of an actin filament severing protein on network properties. The proposed work will impact health by revealing actin network mechanics that play a fundamental role in cellular protrusion essential for cell movements during development as well as metastasis. PUBLIC HEALTH RELEVANCE Dynamic actin networks have been identified as essential for not only cell motility, but also endocytosis, exocytosis, pathogen invasion, T-cell signaling, invadopodia formation, and cell division. Better understanding of how the mechanical microenvironment alters actin network behavior, including its elastic properties and its ability to generate and direct forces for shape change, has the potential to reveal new mechanisms of disease and identify new targets for drug discovery.

描述（由申请人提供）：在体内爬行的细胞必须穿过由细胞-细胞连接、细胞外基质和其他细胞阻碍的复杂景观。中性粒细胞优雅而明显地毫不费力地穿过组织，在一个时刻处于张力下，在下一个时刻处于压缩下，这引发了关于运动细胞如何响应外部以及自我施加的负载的问题。更具体地说，在运动过程中产生细胞突起的肌动蛋白丝网络是如何受到力的影响的？通常认为动态肌动蛋白网络的性质只受肌动蛋白和结合蛋白浓度的控制，这不足以解释细胞如何适应它们的物理环境;必须考虑力在重构或重塑肌动蛋白网络中的作用。我们假设，外部负载机械调节肌动蛋白网络的性能，通过改变网络结构，如丝密度和交联，在负载条件的变化。肌动蛋白网络的机械特性和生长速率响应负载的这种“调整”或适应可能是引导爬行细胞的重要机制，并在其他基于肌动蛋白的过程中发挥关键作用，包括内吞作用，吞噬作用和mechanotransduction。然而，关于动态肌动蛋白网络的物理行为的基本问题仍然没有答案。该建议的重点是Arp 2/3分支肌动蛋白网络的力的响应。使用在体外模型的肌动蛋白网络的增长，我们问几个基本的问题，机械性能，增长率，肌动蛋白结合蛋白在组织网络架构的作用。我们已经开发出一种双悬臂原子力显微镜（AFM）与延时荧光显微镜，具有独特的能力，在受控的加载条件下测量静态和动态肌动蛋白网络的属性。在使用这种技术的初步实验中，我们已经确定了复杂的力学行为的肌动蛋白网络在高负荷和增长率，依赖于加载历史，而不是瞬时负载。该提案将使用一个最小的纯化蛋白质系统，形成不断增长的肌动蛋白网络，以（i）确定负载对机械性能的影响，（ii）跟踪响应于力的生长速率的变化，（iii）检查肌动蛋白丝切断蛋白对网络性能的瞬时影响。这项拟议的工作将通过揭示肌动蛋白网络机制来影响健康，肌动蛋白网络机制在细胞突起中起着重要作用，对细胞在发育和转移过程中的运动至关重要。动态肌动蛋白网络已被确定为不仅对细胞运动，而且对内吞作用、胞吐作用、病原体入侵、T细胞信号传导、侵入伪足形成和细胞分裂至关重要。更好地了解机械微环境如何改变肌动蛋白网络行为，包括其弹性特性及其产生和指导形状变化的力的能力，有可能揭示疾病的新机制并确定药物发现的新靶点。