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T细胞受体信号转导中的脂筏结构域和蛋白质网络

Lipid raft domains and protein networks in T-cell receptor signal transduction.

作者信息

Harder Thomas

机构信息

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.

出版信息

Curr Opin Immunol. 2004 Jun;16(3):353-9. doi: 10.1016/j.coi.2004.03.013.

Abstract

Activation of the T-cell antigen receptor (TCR) is a key event in triggering the physiological responses of T lymphocytes to antigen. The earliest TCR-evoked signalling steps, such as tyrosine phosphorylations, ras activation and induction of Ca(2+) fluxes, are initiated in the T-cell plasma membrane. It has been implicated that cholesterol- and sphingolipid-rich membrane domains, termed lipid rafts, form platforms for the regulation and transduction of TCR signals at the plasma membrane; however, recent experiments have now differentiated distinct roles for lipid-raft-mediated and protein-mediated interactions in the formation of TCR signalling membrane domains.

摘要

T细胞抗原受体(TCR)的激活是触发T淋巴细胞对抗原产生生理反应的关键事件。TCR最早引发的信号传导步骤,如酪氨酸磷酸化、ras激活和Ca(2+)通量的诱导,都在T细胞质膜中启动。有观点认为,富含胆固醇和鞘脂的膜结构域,即脂筏,在质膜上形成了用于调节和转导TCR信号的平台;然而,最近的实验现已区分出脂筏介导的相互作用和蛋白质介导的相互作用在TCR信号传导膜结构域形成中的不同作用。

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