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通过凝集素激活和干扰素-γ处理诱导人细胞中与免疫反应相关的GTP-环化水解酶I mRNA表达。

Induction of GTP-cyclohydrolase I mRNA expression by lectin activation and interferon-gamma treatment in human cells associated with the immune response.

作者信息

Schott K, Gütlich M, Ziegler I

机构信息

GSF-Forschungszentrum für Umwelt und Gesundheit, Institut für Experimentelle Hämatologie, München, Germany.

出版信息

J Cell Physiol. 1993 Jul;156(1):12-6. doi: 10.1002/jcp.1041560103.

Abstract

The development of tetrahydrobiopterin synthesis during lectin stimulation of resting human T lymphocytes (Kerler et al. [1989] FEBS Lett., 250:622-624), the interferon-gamma induced neopterin production by human monocytes/macrophages (Huber et al. [1984] J. Exp. Med., 160:310-316), and the control of tetrahydrobiopterin synthesis in activated T cells by the synergistic action of interferon-gamma and interleukin 2 (Ziegler et al. [1990] J. Biol. Chem. 265:17026-17030) were previously explained by modulation of the apparent GTP-cyclohydrolase I activation. In this study we demonstrate that increases in GTP-cyclohydrolase I activity which occur after lectin induction and after cytokine treatment correlate with increased steady state mRNA levels specific for this enzyme. The enhancement of interferon-gamma induced enzyme activity in primed T cells by interleukin 2 also corresponds to further increases in mRNA expression. The steady state GTP-cyclohydrolase I mRNA levels in primed T cells, however, do not correlate with the steep decline which follows the culmination of enzyme activity 44 hours after treatment. This indicates that the down-regulation of apparent GTP-cyclohydrolase I activity is caused by posttranslational modification of the protein.

摘要

之前,凝集素刺激静息人T淋巴细胞过程中四氢生物蝶呤合成的发展(Kerler等人,[1989]《欧洲生物化学学会联合会快报》,250:622 - 624)、人单核细胞/巨噬细胞受干扰素-γ诱导产生新蝶呤(Huber等人,[1984]《实验医学杂志》,160:310 - 316)以及干扰素-γ和白细胞介素2协同作用对活化T细胞中四氢生物蝶呤合成的控制(Ziegler等人,[1990]《生物化学杂志》265:17026 - 17030),均通过表观GTP-环水解酶I激活的调节来解释。在本研究中,我们证明凝集素诱导后以及细胞因子处理后出现的GTP-环水解酶I活性增加与该酶特异性稳态mRNA水平的升高相关。白细胞介素2增强预处理T细胞中干扰素-γ诱导的酶活性也对应于mRNA表达的进一步增加。然而,预处理T细胞中稳态GTP-环水解酶I mRNA水平与处理后44小时酶活性达到峰值后急剧下降不相关。这表明表观GTP-环水解酶I活性的下调是由该蛋白的翻译后修饰引起的。

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