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鉴定在T细胞激活诱导凋亡过程中诱导产生的一种假定的G蛋白偶联受体。

Identification of a putative G protein-coupled receptor induced during activation-induced apoptosis of T cells.

作者信息

Choi J W, Lee S Y, Choi Y

机构信息

Howard Hughes Medical Institute, The Rockefeller University, New York 10021, USA.

出版信息

Cell Immunol. 1996 Feb 25;168(1):78-84. doi: 10.1006/cimm.1996.0051.

Abstract

During development, self-reactive immature thymocytes are clonally deleted in the thymus, a phenomenon which establishes T cell tolerance (negative selection). It has been shown that the deletion of self-reactive immature T cells in the thymus is mediated by apoptosis upon T cell receptor (TCR) engagement. Apoptosis of immature thymocytes mediated by the TCR requires the expression of a new set of genes. To define which genes are required during the TCR-mediated death of immature thymocytes, we sought to identify genes whose expression is increased during TCR-mediated cell death. Using the technique of differential mRNA display, we have identified a novel gene, TDAG8, which encodes a putative G protein-coupled receptor. The expression of TDAG8 is greatly induced upon activation of T cells by anti-TCR antibody or by phorbol 12-myristate 13-acetate plus ionomycin. The treatment of T cells with glucocorticoids also greatly induces the expression of TDAG8. In mice, TDAG8 is predominantly expressed in thymus and spleen. The tissue-specific expression of TDAG8 and the induction of its expression during cell death of T cells mediated by the TCR or glucocorticoids suggest that it may have a role in activation-induced cell death or differentiation of T cells.

摘要

在发育过程中,自身反应性未成熟胸腺细胞在胸腺中发生克隆性删除,这一现象建立了T细胞耐受性(阴性选择)。研究表明,胸腺中自身反应性未成熟T细胞的删除是由T细胞受体(TCR)结合后介导的凋亡所介导的。TCR介导的未成熟胸腺细胞凋亡需要一组新基因的表达。为了确定在TCR介导的未成熟胸腺细胞死亡过程中需要哪些基因,我们试图鉴定在TCR介导的细胞死亡过程中表达增加的基因。利用差异mRNA显示技术,我们鉴定出一个新基因TDAG8,它编码一种假定的G蛋白偶联受体。用抗TCR抗体或佛波醇12-肉豆蔻酸酯13-乙酸酯加离子霉素激活T细胞后,TDAG8的表达被极大地诱导。用糖皮质激素处理T细胞也能极大地诱导TDAG8的表达。在小鼠中,TDAG8主要在胸腺和脾脏中表达。TDAG8的组织特异性表达及其在TCR或糖皮质激素介导的T细胞死亡过程中的表达诱导表明,它可能在激活诱导的细胞死亡或T细胞分化中起作用。

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