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T细胞活化过程中的质膜分离:探究结构域的顺序

Plasma membrane segregation during T cell activation: probing the order of domains.

作者信息

Harder Thomas, Rentero Carles, Zech Tobias, Gaus Katharina

机构信息

Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom.

出版信息

Curr Opin Immunol. 2007 Aug;19(4):470-5. doi: 10.1016/j.coi.2007.05.002. Epub 2007 Jul 12.

Abstract

T cell activation leads to a segregation of plasma membrane domains to form TCR signalling clusters and eventually immunological synapses. At these T cell activation sites signalling protein networks reside in plasma membrane regions which adopt a highly ordered physical state. Studies of reconstituted model membranes suggest that aggregation of lipid raft-favouring membrane components may trigger this lipid ordering and condensation of membrane domains in T cells. Activation-induced protein-protein interactions such as anchorage to the cytoskeleton drive this condensation of the plasma membrane. Elucidating the functional role and specific molecular mechanisms of lipid ordering at these domains in the T cell activation cascade will be an essential element in understanding the transmission of outside signals into intracellular responses.

摘要

T细胞活化导致质膜结构域分离,形成T细胞受体(TCR)信号簇,并最终形成免疫突触。在这些T细胞活化位点,信号蛋白网络存在于处于高度有序物理状态的质膜区域。对重组模型膜的研究表明,有利于脂筏形成的膜成分聚集可能触发T细胞中这种膜结构域的脂质有序化和凝聚。激活诱导的蛋白质-蛋白质相互作用,如与细胞骨架的锚定,驱动质膜的这种凝聚。阐明T细胞活化级联反应中这些结构域脂质有序化的功能作用和具体分子机制,将是理解外部信号向细胞内反应传递的关键要素。

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