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几何重排的免疫突触揭示形成机制。

Geometrically repatterned immunological synapses uncover formation mechanisms.

作者信息

Figge Marc Thilo, Meyer-Hermann Michael

机构信息

Institute for Theoretical Physics, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.

出版信息

PLoS Comput Biol. 2006 Nov 10;2(11):e171. doi: 10.1371/journal.pcbi.0020171.

DOI:10.1371/journal.pcbi.0020171
PMID:17096594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1635538/
Abstract

The interaction of T cells and antigen-presenting cells is central to adaptive immunity and involves the formation of immunological synapses in many cases. The surface molecules of the cells form a characteristic spatial pattern whose formation mechanisms and function are largely unknown. We perform computer simulations of recent experiments on geometrically repatterned immunological synapses and explain the emerging structure as well as the formation dynamics. Only the combination of in vitro experiments and computer simulations has the potential to pinpoint the kind of interactions involved. The presented simulations make clear predictions for the structure of the immunological synapse and elucidate the role of a self-organizing attraction between complexes of T cell receptor and peptide-MHC molecule, versus a centrally directed motion of these complexes.

摘要

T细胞与抗原呈递细胞的相互作用是适应性免疫的核心,在许多情况下涉及免疫突触的形成。细胞表面分子形成一种特征性的空间模式,其形成机制和功能在很大程度上尚不清楚。我们对最近关于几何重新排列的免疫突触的实验进行了计算机模拟,并解释了出现的结构以及形成动力学。只有体外实验和计算机模拟相结合才有潜力确定所涉及的相互作用类型。所呈现的模拟对免疫突触的结构做出了明确预测,并阐明了T细胞受体与肽-MHC分子复合物之间自组织吸引力的作用,以及这些复合物的中心定向运动的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/24c769802225/pcbi.0020171.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/be04765f9a21/pcbi.0020171.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/706f26948560/pcbi.0020171.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/c6f82c8e4c4c/pcbi.0020171.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/dd77f4d267c6/pcbi.0020171.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/24c769802225/pcbi.0020171.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/be04765f9a21/pcbi.0020171.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/706f26948560/pcbi.0020171.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/c6f82c8e4c4c/pcbi.0020171.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/dd77f4d267c6/pcbi.0020171.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/1664704/24c769802225/pcbi.0020171.g005.jpg

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本文引用的文献

1
Altered TCR signaling from geometrically repatterned immunological synapses.来自几何形状重新排列的免疫突触的TCR信号改变。
Science. 2005 Nov 18;310(5751):1191-3. doi: 10.1126/science.1119238.
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A dynamic view of the immunological synapse.免疫突触的动态观点。
Semin Immunol. 2005 Dec;17(6):400-10. doi: 10.1016/j.smim.2005.09.002. Epub 2005 Nov 2.
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Multifocal structure of the T cell - dendritic cell synapse.T细胞-树突状细胞突触的多焦点结构
长、短受体-配体复合物介导的细胞黏附带中域的线张力和稳定性。
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Computer modeling describes gravity-related adaptation in cell cultures.计算机建模描述了细胞培养中与重力相关的适应。
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Effects of intracellular calcium and actin cytoskeleton on TCR mobility measured by fluorescence recovery.通过荧光恢复测量细胞内钙和肌动蛋白细胞骨架对TCR迁移率的影响。
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T cell receptor microcluster transport through molecular mazes reveals mechanism of translocation.T细胞受体微簇通过分子迷宫的转运揭示了易位机制。
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Testing the organization of the immunological synapse.检测免疫突触的组织结构。
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Pattern formation during T-cell adhesion.T细胞黏附过程中的模式形成。
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Effective membrane model of the immunological synapse.免疫突触的有效膜模型
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In silico models for cellular and molecular immunology: successes, promises and challenges.用于细胞和分子免疫学的计算机模拟模型:成就、前景与挑战。
Nat Immunol. 2003 Oct;4(10):933-6. doi: 10.1038/ni1003-933.
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The immunological synapse balances T cell receptor signaling and degradation.免疫突触平衡T细胞受体信号传导与降解。
Science. 2003 Nov 14;302(5648):1218-22. doi: 10.1126/science.1086507. Epub 2003 Sep 25.
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The diversity of immunological synapses.免疫突触的多样性。
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Low T cell receptor expression and thermal fluctuations contribute to formation of dynamic multifocal synapses in thymocytes.低T细胞受体表达和热波动有助于胸腺细胞中动态多灶性突触的形成。
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