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Effect of nitric oxide donor and gamma irradiation on modifications of ERK and JNK in murine peritoneal macrophages

机译:一氧化氮供体和γ射线照射对小鼠腹膜巨噬细胞ERK和JNK修饰的影响

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摘要

Mitogen activated protein kinases (MAPKs) play an important role in activation, differentiation and proliferation of macrophages. Macrophages, upon activation, produce large amounts of nitric oxide that inhibit the growth of variety of microorganisms and tumor cells. This nitric oxide which is known to interfere with tyrosine phosphorylation may result in changes in the pattern of activation of MAPKs. In a previous study we have found that tyrosine phosphorylation of MAPKs was completely abolished in the presence of nitric oxide donor and radiation but this did not affect the function of macrophages. In this study the other post translational modifications namely nitration and ubiquitination of JNK and ERK have been looked at. Both ERK and JNK were found to be nitrated. However, there was no increase in ubiquitination of ERK and JNK, indicating that ubiquitination, in this case was not a natural consequence of nitration and may serve in signaling. Additionally, when the nitration was extensive, phosphorylation was also inhibited. The activation of substrates of ERK and JNK were looked at to determine the consequences of such modifications. Inhibition of phosphorylation and extensive nitration of JNK did not prevent activation of its substrate, c-jun. This study indicates that ERK and JNK may be under regulation by different type of modifications in macrophages.
机译:丝裂原活化的蛋白激酶(MAPK)在巨噬细胞的活化,分化和增殖中起重要作用。巨噬细胞在激活后会产生大量的一氧化氮,从而抑制各种微生物和肿瘤细胞的生长。已知会干扰酪氨酸磷酸化的一氧化氮可能会导致MAPK激活模式的改变。在先前的研究中,我们发现在存在一氧化氮供体和辐射的情况下,MAPKs的酪氨酸磷酸化被完全消除,但这并不影响巨噬细胞的功能。在这项研究中,还研究了其他翻译后修饰,即JNK和ERK的硝化和泛素化。发现ERK和JNK都被硝化了。但是,ERK和JNK的泛素化没有增加,这表明泛素化在这种情况下不是硝化的自然结果,可能在信号传导中起作用。另外,当硝化作用广泛时,磷酸化作用也受到抑制。研究了ERK和JNK底物的活化,以确定这种修饰的结果。抑制JNK的磷酸化和广泛硝化并不能阻止其底物c-jun的活化。这项研究表明ERK和JNK可能受到巨噬细胞中不同类型修饰的调控。

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