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本文引用的文献

1
Controlling T cells spreading, mechanics and activation by micropatterning.通过微图案化控制 T 细胞的扩散、力学和激活。
Sci Rep. 2021 Mar 24;11(1):6783. doi: 10.1038/s41598-021-86133-1.
2
Influence of external forces on actin-dependent T cell protrusions during immune synapse formation.外力对免疫突触形成过程中肌动蛋白依赖性 T 细胞突起的影响。
Biol Cell. 2021 May;113(5):250-263. doi: 10.1111/boc.202000133. Epub 2021 Feb 10.
3
Diacylglycerol kinase ζ promotes actin cytoskeleton remodeling and mechanical forces at the B cell immune synapse.二酰基甘油激酶 ζ 促进 B 细胞免疫突触处的肌动蛋白细胞骨架重塑和机械力。
Sci Signal. 2020 Apr 14;13(627):eaaw8214. doi: 10.1126/scisignal.aaw8214.
4
Cytoskeletal tension actively sustains the migratory T-cell synaptic contact.细胞骨架张力积极维持迁移 T 细胞突触接触。
EMBO J. 2020 Mar 2;39(5):e102783. doi: 10.15252/embj.2019102783. Epub 2020 Jan 2.
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Actomyosin-driven force patterning controls endocytosis at the immune synapse.肌球蛋白驱动的力模式控制免疫突触处的内吞作用。
Nat Commun. 2019 Jun 28;10(1):2870. doi: 10.1038/s41467-019-10751-7.
6
Real-time deformability cytometry reveals sequential contraction and expansion during neutrophil priming.实时变形细胞术揭示中性粒细胞致敏过程中的顺序收缩和扩张。
J Leukoc Biol. 2019 Jun;105(6):1143-1153. doi: 10.1002/JLB.MA0718-295RR. Epub 2019 Mar 5.
7
T cell receptor-triggered nuclear actin network formation drives CD4 T cell effector functions.T 细胞受体触发的核肌动蛋白网络形成驱动 CD4 T 细胞效应功能。
Sci Immunol. 2019 Jan 4;4(31). doi: 10.1126/sciimmunol.aav1987.
8
Distinct Roles for Bruton's Tyrosine Kinase in B Cell Immune Synapse Formation.布鲁顿酪氨酸激酶在 B 细胞免疫突触形成中的独特作用。
Front Immunol. 2018 Sep 6;9:2027. doi: 10.3389/fimmu.2018.02027. eCollection 2018.
9
Profiling the origin, dynamics, and function of traction force in B cell activation.分析 B 细胞激活中牵引力的起源、动态变化和功能。
Sci Signal. 2018 Aug 7;11(542):eaai9192. doi: 10.1126/scisignal.aai9192.
10
A map of gene expression in neutrophil-like cell lines.中性粒细胞样细胞系的基因表达图谱。
BMC Genomics. 2018 Aug 1;19(1):573. doi: 10.1186/s12864-018-4957-6.

快速的黏弹变化是早期白细胞活化的特征。

Rapid viscoelastic changes are a hallmark of early leukocyte activation.

机构信息

LadHyX, CNRS, Ecole polytechnique, Institut Polytechnique de Paris, Palaiseau, France; Institut de Chimie Physique, CNRS UMR8000, Université Paris-Saclay, Orsay, France.

B Lymphocyte Dynamics Laboratory, Centro Nacional de Biotecnología (CNB)-CSIC, Madrid, Spain.

出版信息

Biophys J. 2021 May 4;120(9):1692-1704. doi: 10.1016/j.bpj.2021.02.042. Epub 2021 Mar 17.

DOI:10.1016/j.bpj.2021.02.042
PMID:33730552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8204340/
Abstract

To accomplish their critical task of removing infected cells and fighting pathogens, leukocytes activate by forming specialized interfaces with other cells. The physics of this key immunological process are poorly understood, but it is important to understand them because leukocytes have been shown to react to their mechanical environment. Using an innovative micropipette rheometer, we show in three different types of leukocytes that, when stimulated by microbeads mimicking target cells, leukocytes become up to 10 times stiffer and more viscous. These mechanical changes start within seconds after contact and evolve rapidly over minutes. Remarkably, leukocyte elastic and viscous properties evolve in parallel, preserving a well-defined ratio that constitutes a mechanical signature specific to each cell type. Our results indicate that simultaneously tracking both elastic and viscous properties during an active cell process provides a new, to our knowledge, way to investigate cell mechanical processes. Our findings also suggest that dynamic immunomechanical measurements can help discriminate between leukocyte subtypes during activation.

摘要

为了完成清除感染细胞和对抗病原体的关键任务,白细胞通过与其他细胞形成特殊的界面来激活。这个关键免疫学过程的物理性质还不太清楚,但理解它们很重要,因为已经证明白细胞会对其机械环境做出反应。使用一种创新的微管流变仪,我们在三种不同类型的白细胞中表明,当受到模拟靶细胞的微球刺激时,白细胞的硬度和粘性最高可增加 10 倍。这些机械变化在接触后几秒钟内开始,并在数分钟内迅速演变。值得注意的是,白细胞的弹性和粘性特性呈平行变化,保持着一种定义明确的比例,构成了每种细胞类型特有的机械特征。我们的研究结果表明,在细胞的主动过程中同时跟踪弹性和粘性特性,为我们所知的一种研究细胞力学过程的新方法。我们的发现还表明,动态免疫力学测量可以帮助在激活过程中区分白细胞亚型。