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缺乏 G 蛋白信号激活物 3(AGS3)的白细胞中趋化因子信号整合缺陷。

Defective chemokine signal integration in leukocytes lacking activator of G protein signaling 3 (AGS3).

机构信息

Department of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina 29425.

Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, South Carolina 29425.

出版信息

J Biol Chem. 2014 Apr 11;289(15):10738-10747. doi: 10.1074/jbc.M113.515031. Epub 2014 Feb 26.

Abstract

Activator of G-protein signaling 3 (AGS3, gene name G-protein signaling modulator-1, Gpsm1), an accessory protein for G-protein signaling, has functional roles in the kidney and CNS. Here we show that AGS3 is expressed in spleen, thymus, and bone marrow-derived dendritic cells, and is up-regulated upon leukocyte activation. We explored the role of AGS3 in immune cell function by characterizing chemokine receptor signaling in leukocytes from mice lacking AGS3. No obvious differences in lymphocyte subsets were observed. Interestingly, however, AGS3-null B and T lymphocytes and bone marrow-derived dendritic cells exhibited significant chemotactic defects as well as reductions in chemokine-stimulated calcium mobilization and altered ERK and Akt activation. These studies indicate a role for AGS3 in the regulation of G-protein signaling in the immune system, providing unexpected venues for the potential development of therapeutic agents that modulate immune function by targeting these regulatory mechanisms.

摘要

G 蛋白信号转导激活因子 3(AGS3,基因名称为 G 蛋白信号转导调节剂-1,Gpsm1)是 G 蛋白信号转导的辅助蛋白,在肾脏和中枢神经系统中具有功能作用。在这里,我们表明 AGS3 在脾脏、胸腺和骨髓来源的树突状细胞中表达,并在白细胞激活时上调。我们通过研究缺乏 AGS3 的小鼠的白细胞中趋化因子受体信号转导来探索 AGS3 在免疫细胞功能中的作用。未观察到淋巴细胞亚群的明显差异。然而,有趣的是,AGS3 缺失的 B 和 T 淋巴细胞以及骨髓来源的树突状细胞表现出明显的趋化缺陷,以及趋化因子刺激的钙动员减少和 ERK 和 Akt 激活改变。这些研究表明 AGS3 在免疫系统中 G 蛋白信号转导的调节中起作用,为通过靶向这些调节机制来调节免疫功能的潜在治疗药物的开发提供了意想不到的途径。

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