Suppr超能文献

T细胞黏附会触发免疫突触远端的早期信号传导极点。

T cell adhesion triggers an early signaling pole distal to the immune synapse.

作者信息

Guedj Chloé, Abraham Nicolas, Jullié Damien, Randriamampita Clotilde

机构信息

INSERM, U1016, Institut Cochin, Infection, Immunity and Inflammation Department, 22 rue Méćhain, Paris 75014, France CNRS, UMR8104, Paris 75014, France Université Paris Descartes, Sorbonne Paris Cité, Paris 75014, France.

INSERM, U1016, Institut Cochin, Infection, Immunity and Inflammation Department, 22 rue Méćhain, Paris 75014, France CNRS, UMR8104, Paris 75014, France Université Paris Descartes, Sorbonne Paris Cité, Paris 75014, France

出版信息

J Cell Sci. 2016 Jul 1;129(13):2526-37. doi: 10.1242/jcs.182311. Epub 2016 May 16.

Abstract

The immunological synapse forms at the interface between a T cell and an antigen-presenting cell after foreign antigen recognition. The immunological synapse is considered to be the site where the signaling cascade leading to T lymphocyte activation is triggered. Here, we show that another signaling region can be detected before formation of the synapse at the opposite pole of the T cell. This structure appears during the first minute after the contact forms, is transient and contains all the classic components that have been previously described at the immunological synapse. Its formation is independent of antigen recognition but is driven by adhesion itself. It constitutes a reservoir of signaling molecules that are potentially ready to be sent to the immunological synapse through a microtubule-dependent pathway. The antisynapse can thus be considered as a pre-synapse that is triggered independently of antigen recognition.

摘要

在识别外来抗原后,免疫突触在T细胞与抗原呈递细胞之间的界面形成。免疫突触被认为是触发导致T淋巴细胞活化的信号级联反应的位点。在此,我们表明在突触形成之前,可以在T细胞相对极检测到另一个信号区域。这种结构在接触形成后的第一分钟内出现,是短暂的,并且包含先前在免疫突触中描述的所有经典成分。其形成独立于抗原识别,而是由黏附本身驱动。它构成了一个信号分子库,这些信号分子可能随时准备通过微管依赖性途径被输送到免疫突触。因此,反突触可以被视为独立于抗原识别而触发的前突触。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验