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T细胞抗原受体与Fcγ受体相互作用对T细胞的功能影响。

Functional consequences of the interaction between T-cell antigen receptors and Fc gamma Rs on T cells.

作者信息

Kwack K, Verbeek J S, van de Winkel J G, Cappel P, Nambu M, Hagen M, Weinstock J V, Lynch R G, Sandor M

机构信息

Department of Pathology College of Medicine, University of Iowa, Iowa City, USA.

出版信息

Immunol Lett. 1995 Jan;44(2-3):139-43. doi: 10.1016/0165-2478(94)00205-6.

Abstract

Two series of experiments are presented indicating that Fc gamma II receptors can interfere with the antigen receptor-induced signaling on T cells. It has been previously described that a 13 amino acid motif on the cytoplasmic portion of Fc gamma II beta 1 can abrogate the antigen receptor-initiated signals mediated through consensus motifs present on the cytoplasmic portion of Ig alpha and Ig beta chains. Similar activating motifs are crucial to T-cell receptor (TCR) signaling. A splenic gamma/delta T-cell hybridoma that expressed the Fc gamma RII beta 1 receptor helped to establish that this receptor can also interfere with TCR-induced activation. The cytoplasmic portion of human Fc gamma RIIa has an activation motif similar to the activation motifs present on the TCR. Using a transgenic mouse in which the T cells express the human Fc gamma RIIa transgene, we demonstrated that despite the common activation motif, the TCR and human Fc gamma RIIa-induced signals are different. Additionally, the human Fc gamma RIIa expressing T cells exhibit an enhanced TCR response both in vitro and in vivo.

摘要

本文展示了两个系列的实验,表明FcγII受体可干扰T细胞上抗原受体诱导的信号传导。先前已有研究表明,FcγIIβ1胞质部分的一个13个氨基酸的基序可消除通过Igα和Igβ链胞质部分上存在的共有基序介导的抗原受体启动信号。类似的激活基序对T细胞受体(TCR)信号传导至关重要。表达FcγRIIβ1受体的脾γ/δT细胞杂交瘤有助于证实该受体也可干扰TCR诱导的激活。人FcγRIIa的胞质部分具有与TCR上存在的激活基序相似的激活基序。利用T细胞表达人FcγRIIa转基因的转基因小鼠,我们证明尽管存在共同的激活基序,但TCR和人FcγRIIa诱导的信号是不同的。此外,表达人FcγRIIa的T细胞在体外和体内均表现出增强的TCR反应。

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