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Regulation of inducible nitric oxide synthase expression in beta cells by environmental factors: heavy metals.

机译:环境因素:重金属对β细胞中诱导型一氧化氮合酶表达的调节。

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摘要

The expression of inducible NO synthase (iNOS) in pancreatic islet beta cells modulates endocrine cell functions and, at very high levels of NO production causes beta-cell death. We tested the hypothesis that environmental factors such as heavy-metal salts modulate iNOS expression in beta cells. A rat beta-cell line (insulinoma RINm5F) was cultured in the presence of low-dose interleukin (IL)-1beta for suboptimal induction of iNOS. PbCl2 (0. 1-10 microM) dose-dependently increased NO (measured as nitrite) formation (P<0.001). In contrast, HgCl2 suppressed nitrite production (0.1-10 microM, P<0.05). Measurements of iNOS activity by determining citrulline levels confirmed the potentiating effect of PbCl2 (P<0.05). There was a narrow time window of heavy-metal actions, ranging from -24 h (Hg2+) or -3 h (Pb2+) to +2 h, relative to the addition of IL-1beta. By semi-quantitative reverse transcriptase-PCR, enhanced levels of iNOS mRNA were found in the presence of Pb2+ (P<0.05) and decreased levels in the presence of Hg2+. The amount of iNOS protein as determined by Western blotting was increased in the presence of Pb2+. We conclude that Pb2+ upregulates and Hg2+ suppresses iNOS gene expression at the level of transcription, probably by acting on the signalling pathway. These observations may have important implications for understanding pathological effects of environmental factors on endocrine organ functions.
机译:胰岛β细胞中诱导型NO合酶(iNOS)的表达调节内分泌细胞功能,并且在很高的NO产生水平下会导致β细胞死亡。我们测试了这样的假设,即环境因素(例如重金属盐)调节β细胞中iNOS的表达。在低剂量白介素(IL)-1beta存在的情况下培养大鼠β细胞系(胰岛素瘤RINm5F),以最佳方式诱导iNOS。 PbCl2(0. 1-10 microM)剂量依赖性增加NO(以亚硝酸盐计)的形成(P <0.001)。相反,HgCl2抑制了亚硝酸盐的产生(0.1-10 microM,P <0.05)。通过测定瓜氨酸水平的iNOS活性测量证实了PbCl2的增强作用(P <0.05)。相对于添加IL-1beta,重金属作用的时间窗口很窄,范围从-24 h(Hg2 +)或-3 h(Pb2 +)到+2 h。通过半定量逆转录酶-PCR,在Pb2 +存在下,iNOS mRNA的水平升高(P <0.05),在Hg2 +存在下,iNOS mRNA的水平降低。在Pb2 +存在下,通过蛋白质印迹法测定的iNOS蛋白的量增加了。我们得出结论,Pb2 +上调,Hg2 +在转录水平上抑制iNOS基因表达,可能是通过作用于信号通路。这些观察结果可能对理解环境因素对内分泌器官功能的病理影响具有重要意义。

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