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通过在肥大细胞系中过表达Gαz增强肿瘤坏死因子-α的合成。

Enhancement of TNF-alpha synthesis by overexpression of G alpha z in a mast cell line.

作者信息

Baumgartner R A, Hirasawa N, Ozawa K, Gusovsky F, Beaven M A

机构信息

Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

J Immunol. 1996 Aug 15;157(4):1625-9.

PMID:8759748
Abstract

Ag stimulation of mast cells via the IgE receptor (Fc epsilon RI) elicits production and release of numerous cytokines. This activation of Fc epsilon RI initiates various tyrosine kinase-dependent signaling cascades, which ultimately result in the de novo synthesis of cytokines. To date, no heterotrimeric G proteins have been implicated in this process. Here we report that the alpha subunit of the heterotrimeric G protein, Gz, can regulate production of the cytokine, TNF-alpha. The alpha subunit was overexpressed in a cultured mast cell line (RBL-2H3) known to contain G alpha z. In stimulated cells, overexpression of G alpha z significantly enhanced the production of TNF-alpha. This effect of G alpha z appeared to be restricted in that constitutive synthesis of the cytokine, TGF-beta, and Ag-stimulation of the phosphoinositide-dependent secretory pathway were not significantly affected. Thus, G alpha z, a heterotrimeric G protein, appeared to modulate the stimulatory pathways for induction of TNF-alpha synthesis in RBL-2H3 cells.

摘要

通过IgE受体(FcεRI)对肥大细胞进行抗原刺激会引发多种细胞因子的产生和释放。FcεRI的这种激活会启动各种酪氨酸激酶依赖性信号级联反应,最终导致细胞因子的从头合成。迄今为止,尚无异源三聚体G蛋白参与此过程的相关报道。在此我们报告,异源三聚体G蛋白Gz的α亚基可调节细胞因子肿瘤坏死因子-α(TNF-α)的产生。α亚基在已知含有Gαz的培养肥大细胞系(RBL-2H3)中过表达。在受刺激的细胞中,Gαz的过表达显著增强了TNF-α的产生。Gαz的这种作用似乎具有局限性,因为细胞因子转化生长因子-β(TGF-β)的组成型合成以及对磷酸肌醇依赖性分泌途径的抗原刺激均未受到显著影响。因此,异源三聚体G蛋白Gαz似乎可调节RBL-2H3细胞中诱导TNF-α合成的刺激途径。

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