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T细胞抗原受体复合物的多个组分在激活后会发生酪氨酸磷酸化。

Multiple components of the T cell antigen receptor complex become tyrosine-phosphorylated upon activation.

作者信息

Qian D, Griswold-Prenner I, Rosner M R, Fitch F W

机构信息

Department of Pathology, University of Chicago, Illinois 60637.

出版信息

J Biol Chem. 1993 Feb 25;268(6):4488-93.

PMID:8440731
Abstract

Triggering of the multicomponent T cell antigen receptor (TCR) complex results in several biochemical processes which are critical for the functional activation of T lymphocytes. One common process is the tyrosine phosphorylation of several proteins, including the TCR zeta chain. Here we show that in addition to TCR zeta, other subunits (CD3 gamma, CD3 delta, and CD3 epsilon) of the TCR complex can also be tyrosine-phosphorylated in response to antigen receptor stimulation. This rapid phosphorylation was detected in several mature murine T cell subsets, including CD4+ type 1 and 2 helper cells (TH1 and TH2). Therefore, tyrosine phosphorylation of multiple TCR components in addition to TCR zeta may be an important event during the initiation of the signaling cascade leading to T cell activation.

摘要

多组分T细胞抗原受体(TCR)复合物的触发会引发若干对T淋巴细胞功能激活至关重要的生化过程。一个常见过程是几种蛋白质的酪氨酸磷酸化,包括TCR ζ链。在此我们表明,除了TCR ζ链外,TCR复合物的其他亚基(CD3γ、CD3δ和CD3ε)也可因抗原受体刺激而发生酪氨酸磷酸化。在几个成熟的小鼠T细胞亚群中检测到了这种快速磷酸化,包括CD4 + 1型和2型辅助性T细胞(TH1和TH2)。因此,除TCR ζ链外,多种TCR组分的酪氨酸磷酸化可能是导致T细胞激活的信号级联反应起始过程中的一个重要事件。

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