Quantitative Study of T-cell Polarization

T 细胞极化的定量研究

• 批准号: 7455822
• 负责人: IVAN V MALY
• 金额: $ 26.98万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-03 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7455822
• 关键词: Actins; Actomyosin; Adhesions; Antigen-Presenting Cells; Biomedical Research; Biomimetics; Cell Communication; Cell Shape; Cells; Cellular biology; Centrosome; Complex; Computer Simulation; Condition; Coupling; Data; Dimensions; Drug Formulations; Dynein ATPase; Experimental Models; Fiber; Golgi Apparatus; Grant; Immigration; Immune; Immune response; Immune system; Jurkat Cells; Kinesin; Kinetics; Knowledge; Lead; Life; Measurement; Mechanics; Methodology; Microscopy; Microtubules; Modeling; Molecular; Molecular Motors; Movement; Myosin ATPase; Numbers; Organelles; Outcome; Pathway interactions; Positioning Attribute; Process; Property; Quantitative Microscopy; Regulation; Research; Research Personnel; Surface; System; T-Lymphocyte; Testing; base; cell motility; design; migration; neoplastic cell; novel; research study

DESCRIPTION (provided by applicant): The objective of this project is to put our understanding of T cell polarization on a firm quantitative basis. T cells of the immune system polarize, i.e. orient themselves, toward their targets, such as infected or tumor cells to be eliminated. The crucial component of the T cell polarization is reorientation of the centrosome toward the target. Although a number of molecular pathways involved in regulation of this process have been identified, even a general understanding is lacking as to the mechanism of the process itself. New data lead us to hypothesize, contrary to the accepted notion, that the basic mechanism is whole-cell movement and deformation on contact with the target, a process directed toward whole-cell structural optimization. First, we will employ a simplified experimental system of T cells stimulated with planar biomimetic substrates to elucidate the basic features of the centrosome reorientation. This will be achieved through combination of computational modeling with quantitative, multidimensional, live-cell microscopy. Next, the contribution of specific force-generating intracellular processes (molecular motors, cytoskeletal dynamics) to the centrosome translocation will be determined by enriching the basic model with specific numerical models of these processes and comparing the predictions with experiments in which the specific molecular activities are modulated. Lastly, we will use the achieved understanding of the simplified system amenable to high- throughput measurements to extrapolate our knowledge computationally to the realistic case of the T cell- target cell interaction. The predictions will be tested by means of quantitative microscopy and the additional features found in the cell-cell interactions added to the computer model. The outcome of the project will be not only rigorous understanding of the biomedically significant phenomenon of centrosome polarization in the immune cells, formalized in a predictive computer model, but also a substantial empirical improvement of the new methodology of quantitative biomedical research.

描述（由申请人提供）：本项目的目的是将我们对T细胞极化的理解建立在坚实的定量基础上。免疫系统的T细胞朝向它们的靶细胞，例如被感染的细胞或待消除的肿瘤细胞，定向。T细胞极化的关键组成部分是中心体朝向靶的重定向。虽然已经确定了许多参与调节这一过程的分子途径，但对这一过程本身的机制甚至缺乏一般性的了解。新的数据使我们假设，与公认的概念相反，基本机制是与目标接触时的全细胞运动和变形，这是一个指向全细胞结构优化的过程。首先，我们将采用一个简化的实验系统的T细胞刺激与平面仿生基板阐明中心体重新定位的基本特征。这将通过计算建模与定量，多维，活细胞显微镜相结合来实现。接下来，特定的力产生的细胞内过程（分子马达，细胞骨架动力学）的中心体易位的贡献将通过丰富的基本模型与这些过程的特定的数值模型，并比较的预测与实验中的特定分子活动进行调制。最后，我们将使用对适合高通量测量的简化系统的所获得的理解来计算地将我们的知识外推到T细胞-靶细胞相互作用的现实情况。这些预测将通过定量显微镜进行测试，并将细胞-细胞相互作用中发现的其他特征添加到计算机模型中。该项目的成果将不仅是对免疫细胞中中心体极化的生物医学重要现象的严格理解，在预测计算机模型中正式化，而且还将对定量生物医学研究的新方法进行实质性的经验改进。