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电离辐射增强了干扰素-γ和/或脂多糖在小鼠巨噬细胞系中诱导一氧化氮合酶的作用:肿瘤坏死因子-α的作用

Ionizing radiation potentiates the induction of nitric oxide synthase by IFN-gamma and/or LPS in murine macrophage cell lines: role of TNF-alpha.

作者信息

McKinney L C, Aquilla E M, Coffin D, Wink D A, Vodovotz Y

机构信息

Department of Radiation Pathophysiology and Toxicology, Armed Forces Radiobiology Research Institute, Bethesda, Maryland, USA.

出版信息

J Leukoc Biol. 1998 Oct;64(4):459-66. doi: 10.1002/jlb.64.4.459.

Abstract

Macrophages are activated to become cytotoxic by a highly coordinated set of cytokine signals. Ionizing radiation can mimic cytokine signals and lead to enhanced states of activation. We tested the ability of gamma-radiation, alone and with interferon-gamma (IFN-gamma) and/or lipopolysaccharide (LPS), to induce nitric oxide (NO) production in J774.1 and RAW264.7 murine macrophages. NO was induced weakly, moderately, or strongly by IFN-gamma alone, LPS alone, or IFN-gamma + LPS, respectively. Radiation alone (0.5-50 Gy) did not induce NO, but enhanced NO production in a dose-dependent manner (0.5-5 Gy) when cells were exposed to IFN-gamma or LPS 24 h post-irradiation. Immunoblots showed parallel induction of nitric oxide synthase (NOS2). Application of anti-tumor necrosis factor alpha (TNF-alpha) antibody before irradiation blocked induction of NO by IFN-gamma. We conclude (1) that irradiated cells produce more NO in response to either IFN-gamma or LPS and (2) that the increase is mediated by induction of TNF-alpha.

摘要

巨噬细胞通过一组高度协调的细胞因子信号被激活,从而具有细胞毒性。电离辐射可模拟细胞因子信号并导致激活状态增强。我们测试了γ射线单独以及与γ干扰素(IFN-γ)和/或脂多糖(LPS)联合使用时,在J774.1和RAW264.7小鼠巨噬细胞中诱导一氧化氮(NO)产生的能力。单独使用IFN-γ、单独使用LPS或IFN-γ + LPS分别诱导出弱、中、强水平的NO。单独的辐射(0.5 - 50 Gy)不会诱导NO产生,但当细胞在照射后24小时暴露于IFN-γ或LPS时,辐射会以剂量依赖性方式(0.5 - 5 Gy)增强NO的产生。免疫印迹显示一氧化氮合酶(NOS2)的平行诱导。在照射前应用抗肿瘤坏死因子α(TNF-α)抗体可阻断IFN-γ诱导的NO产生。我们得出结论:(1)受照射的细胞对IFN-γ或LPS的反应会产生更多的NO;(2)这种增加是由TNF-α的诱导介导的。

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