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通过激活G蛋白偶联趋化因子受体进行基因转录。

Gene transcription through activation of G-protein-coupled chemoattractant receptors.

作者信息

Ye R D, Pan Z, Kravchenko V V, Browning D D, Prossnitz E R

机构信息

Department of Immunology, Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

Gene Expr. 1996;5(4-5):205-15.

Abstract

Receptors for leukocyte chemoattractants, including chemokines, are traditionally considered to be responsible for the activation of special leukocyte functions such as chemotaxis, degranulation, and the release of superoxide anions. Recently, these G-protein-coupled serpentine receptors have been found to transduce signals leading to gene transcription and translation in leukocytes. Transcription factors, such as NF kappa B and AP-1, are activated upon stimulation of the cells with several chemoattractants at physiologically relevant concentrations. Activation of transcription factors through these receptors involves G-protein coupling and the activation of protein kinases. The underlying signaling pathways appear to be different from those utilized by TNF-alpha, a better characterized cytokine that induces the transcription of immediate-early genes. Chemoattractants stimulate the expression of several inflammatory cytokines and chemokines, which in turn may activate their respective receptors and initiate an autocrine regulatory mechanism for persistent cytokine and chemokine gene expression.

摘要

包括趋化因子在内的白细胞趋化剂受体,传统上被认为负责激活特殊的白细胞功能,如趋化作用、脱颗粒以及超氧阴离子的释放。最近,这些G蛋白偶联的蛇形受体已被发现可转导导致白细胞中基因转录和翻译的信号。转录因子,如核因子κB(NFκB)和激活蛋白-1(AP-1),在生理相关浓度下用几种趋化剂刺激细胞时会被激活。通过这些受体激活转录因子涉及G蛋白偶联和蛋白激酶的激活。潜在的信号通路似乎不同于肿瘤坏死因子-α(TNF-α)所利用的信号通路,TNF-α是一种特征更明确的细胞因子,可诱导即早基因的转录。趋化剂刺激几种炎性细胞因子和趋化因子的表达,反过来这些因子可能激活它们各自的受体,并启动一种自分泌调节机制以持续表达细胞因子和趋化因子基因。

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