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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.
期刊论文(8)
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会议论文
An experimental and computational study of effects of microtubule stabilization on T-cell polarity.
微管稳定对T细胞极性的影响的实验和计算研究。
DOI: 10.1371/journal.pone.0003861
发表时间: 2008
期刊: PLOS ONE
影响因子: 3.7
作者: [Baratt, Arie, Arkhipov, Sergey N., Maly, Ivan V.]
通讯作者: Maly, Ivan V.
Deterministic mechanical model of T-killer cell polarization reproduces the wandering of aim between simultaneously engaged targets.
T 杀伤细胞极化的确定性力学模型再现了同时攻击的目标之间的目标漂移。
DOI: 10.1371/journal.pcbi.1000260
发表时间: 2009
期刊: PLoS computational biology
影响因子: 4.3
作者: [Kim,MunJu, Maly,IvanV]
通讯作者: Maly,IvanV
Systems biomechanics of centrosome positioning: A conserved complexity.
中心体定位的系统生物力学:保守的复杂性。
DOI: 10.4161/cib.4.2.14548
发表时间: 2011
期刊: Communicative & integrative biology
影响因子: --
作者: [Maly,IvanV]
通讯作者: Maly,IvanV
DOI: 10.1371/journal.pone.0000633
发表时间: 2007-07-25
期刊: PloS one
影响因子: 3.7
作者: [Arkhipov SN, Maly IV]
通讯作者: Maly IV
Quantitative Study of T-cell Polarization
Quantitative Study of T-cell Polarization
Quantitative Study of T-cell Polarization
Quantitative Study of T-cell Polarization
国内基金
海外基金
由actomyosin介导的集体性细胞迁移对唇腭裂发生的影响的研究
  • 批准号:
    82360313
  • 项目类别:
    地区科学基金项目
  • 资助金额:
    32万元
  • 批准年份:
    2023
  • 负责人:
    滕藤
  • 依托单位: