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Impact of tumour necrosis factor-α and interferon-γ on tetrahydrobiopterin synthesis in murine fibroblasts and macrophages

机译:肿瘤坏死因子-α和干扰素-γ对鼠成纤维细胞和巨噬细胞四氢生物蝶呤合成的影响

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pTumour necrosis factor-alpha causes an up to 30-fold induction of GTP cyclohydrolase I (EC 3.5.4.16) activity in murine dermal fibroblasts in a dose-dependent manner. Owing to the high constitutive activities of 6-pyruvoyltetrahydropterin synthase and sepiapterin reductase (EC 1.1.1.153), this potentiates biosynthesis of tetrahydrobiopterin. Murine macrophages already contain high activities of GTP cyclohydrolase I when unstimulated, and this is further augmented up to 4-fold by tumour necrosis factor-alpha/interferon-gamma. In Western blots an antiserum to murine liver GTP cyclohydrolase I does not stain cell extracts with high enzyme activities, suggesting that the cytokine induced peripheral form of GTP cyclohydrolase I might differ from the liver form./p
机译:肿瘤坏死因子-α以剂量依赖的方式在鼠类真皮成纤维细胞中诱导高达30倍的GTP环水解酶I(EC 3.5.4.16)活性诱导。由于6-丙酮酰基四氢蝶呤合酶和Sepaapterin还原酶(EC 1.1.1.153)的高组成活性,因此可以增强四氢生物蝶呤的生物合成。小鼠巨噬细胞在不被刺激时已经具有高活性的GTP环水解酶I,并且通过肿瘤坏死因子-α/干扰素-γ进一步增加至4倍。在Western印迹中,鼠肝GTP环水解酶I的抗血清不能染色具有高酶活性的细胞提取物,这表明细胞因子诱导的GTP环水解酶I的外周形式可能不同于肝脏形式。

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