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前沿:鉴定孤儿趋化因子受体GPR-9-6为CCR9,即趋化因子TECK的受体。

Cutting edge: identification of the orphan chemokine receptor GPR-9-6 as CCR9, the receptor for the chemokine TECK.

作者信息

Zaballos A, Gutiérrez J, Varona R, Ardavín C, Márquez G

机构信息

Departamento de Inmunología y Oncología, Centro Nacional de Biotecnología, Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

J Immunol. 1999 May 15;162(10):5671-5.

Abstract

Thymus-expressed chemokine (TECK) has been reported to chemoattract dendritic cells, thymocytes, and activated macrophages. Here, we show that TECK is a specific agonist for a human orphan receptor called GPR-9-6. We have determined the cDNA sequence of human GPR-9-6 and cloned the corresponding murine cDNA. Human and murine GPR-9-6 expression is very high in the thymus and low in lymph nodes and spleen. RT-PCR analysis of murine GPR-9-6 expression on murine FACS-sorted thymocyte subpopulations showed that this gene is expressed in both immature and mature T cells. Additions of human or murine TECK to HEK 293/human GPR-9-6 and HEK 293/murine GPR-9-6 transfectants provoked intracytoplasmic calcium mobilization. Human TECK also induced the in vitro migration of HEK 293/human GPR-9-6 cells. These results confirm that GPR-9-6 is a specific receptor for TECK. According to the established nomenclature system, we propose to rename GPR-9-6 as CC chemokine receptor 9 (CCR9).

摘要

胸腺表达趋化因子(TECK)据报道可趋化树突状细胞、胸腺细胞和活化的巨噬细胞。在此,我们表明TECK是一种名为GPR-9-6的人类孤儿受体的特异性激动剂。我们已确定人类GPR-9-6的cDNA序列并克隆了相应的小鼠cDNA。人类和小鼠GPR-9-6在胸腺中表达非常高,而在淋巴结和脾脏中表达较低。对小鼠FACS分选的胸腺细胞亚群上小鼠GPR-9-6表达的RT-PCR分析表明,该基因在未成熟和成熟T细胞中均有表达。将人类或小鼠TECK添加到HEK 293/人类GPR-9-6和HEK 293/小鼠GPR-9-6转染细胞中会引发胞浆内钙动员。人类TECK还诱导了HEK 293/人类GPR-9-6细胞的体外迁移。这些结果证实GPR-9-6是TECK的特异性受体。根据既定的命名系统,我们建议将GPR-9-6重新命名为CC趋化因子受体9(CCR9)。

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