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Upregulation of phagocyte-like NADPH oxidase by cytokines in pancreatic beta-cells: Attenuation of oxidative and nitrosative stress by 2-bromopalmitate

机译:胰腺β细胞中细胞因子上调吞噬细胞样NADPH氧化酶的上调:2-溴脓性氧化和氮化应激的衰减

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摘要

Phagocyte-like NADPH oxidase (Nox2) has been shown to play regulatory roles in the metabolic dysfunction of the islet β-cell under the duress of glucolipotoxic conditions and exposure to proinflammatory cytokines. However, the precise mechanisms underlying Nox2 activation by these stimuli remain less understood. To this end, we report a time-dependent phosphorylation of p47phox, a cytosolic subunit of Nox2, by cytomix (IL-1β+TNFα+IFNγ) in insulin-secreting INS-1 832/13 cells. Furthermore, cytomix induced the expression of gp91phox, a membrane component of Nox2. 2-Bromopalmitate (2-BP), a known inhibitor of protein palmitoylation, markedly attenuated cytokine-induced, Nox2-mediated reactive oxygen species (ROS) generation and inducible nitric oxide synthase-mediated nitric oxide (NO) generation. However, 2-BP failed to exert any significant effects on cytomix-induced CHOP expression, a marker for endoplasmic reticulum stress. Together, our findings identify palmitoyltransferase as a target for inhibition of cytomix-induced oxidative (ROS generation) and nitrosative (NO generation) stress in the pancreatic β-cell.
机译:在糖脂毒性条件下和暴露于促炎细胞因子的条件下,吞噬细胞样NADPH氧化酶(Nox2)已被证明在胰岛β细胞的代谢功能异常中起调节作用。但是,仍不清楚这些刺激激活Nox2的确切机制。为此,我们报告了分泌胰岛素的INS-1 832/13细胞中细胞混合物(IL-1β+TNFα+IFNγ)对p47phox(Nox2的胞质亚基)的时间依赖性磷酸化。此外,细胞混合物还诱导了Nox2的膜成分gp91phox的表达。 2-溴棕榈酸酯(2-BP)是已知的蛋白质棕榈酰化抑制剂,可显着减弱细胞因子诱导的由Nox2介导的活性氧(ROS)的产生和诱导型一氧化氮合酶介导的一氧化氮(NO)的产生。但是,2-BP未能对细胞混合物诱导的CHOP表达(内质网应激的标志物)产生任何显着影响。在一起,我们的发现确定棕榈酰转移酶是抑制胰岛β细胞中细胞混合物诱导的氧化(ROS生成)和亚硝化(NO生成)应激的靶标。

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