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T 淋巴细胞激活中的机械感知。

Mechanosensing in T lymphocyte activation.

机构信息

Department of Biomedical Engineering, Columbia University, New York, New York, USA.

出版信息

Biophys J. 2012 Jan 18;102(2):L5-7. doi: 10.1016/j.bpj.2011.12.011.

DOI:10.1016/j.bpj.2011.12.011
PMID:22339876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3260692/
Abstract

Mechanical forces play an increasingly recognized role in modulating cell function. This report demonstrates mechanosensing by T cells, using polyacrylamide gels presenting ligands to CD3 and CD28. Naive CD4 T cells exhibited stronger activation, as measured by attachment and secretion of IL-2, with increasing substrate elastic modulus over the range of 10-200 kPa. By presenting these ligands on different surfaces, this report further demonstrates that mechanosensing is more strongly associated with CD3 rather than CD28 signaling. Finally, phospho-specific staining for Zap70 and Src family kinase proteins suggests that sensing of substrate rigidity occurs at least in part by processes downstream of T-cell receptor activation. The ability of T cells to quantitatively respond to substrate rigidly provides an intriguing new model for mechanobiology.

摘要

机械力在调节细胞功能方面发挥着越来越重要的作用。本报告通过展示在不同的表面呈现配体的聚丙稀酰胺凝胶来证明 T 细胞的机械敏感性,这种方法可以测量 CD3 和 CD28 上的配体。在 10-200kPa 的范围内,随着基质弹性模量的增加,幼稚 CD4 T 细胞的附着和白介素-2 的分泌显示出更强的激活作用。通过在不同的表面呈现这些配体,本报告进一步表明,机械敏感性与 CD3 信号而非 CD28 信号更为密切相关。最后,磷酸化特异性标记 Zap70 和 Src 家族激酶蛋白表明,细胞受体激活下游的过程至少在一定程度上参与了对基质刚性的感知。T 细胞定量响应基质刚性的能力为机械生物学提供了一个有趣的新模型。

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本文引用的文献

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Cutting Edge: mechanical forces acting on T cells immobilized via the TCR complex can trigger TCR signaling.前沿:通过 T 细胞受体复合物固定的 T 细胞上的机械力作用可以触发 TCR 信号转导。
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The alphabeta T cell receptor is an anisotropic mechanosensor.αβ T细胞受体是一种各向异性的机械传感器。
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T cell antigen receptor signaling and immunological synapse stability require myosin IIA.T细胞抗原受体信号传导和免疫突触稳定性需要肌球蛋白IIA。
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Proc Natl Acad Sci U S A. 2008 Jun 3;105(22):7791-6. doi: 10.1073/pnas.0710295105. Epub 2008 May 27.
5
Cell adhesion molecules and actin cytoskeleton at immune synapses and kinapses.免疫突触和亲和突触处的细胞黏附分子与肌动蛋白细胞骨架
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