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泛素化途径调节巨噬细胞的增殖和存活。

Neddylation pathway regulates the proliferation and survival of macrophages.

机构信息

College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, China.

出版信息

Biochem Biophys Res Commun. 2013 Mar 15;432(3):494-8. doi: 10.1016/j.bbrc.2013.02.028. Epub 2013 Feb 14.

Abstract

Neddylation is a new type of protein post-translational modification which adds the ubiquitin-like molecule Nedd8 to target proteins. The well-identified targets of neddylation are cullins, which serve as essential components of Cullin-RING E3 ligases (CRL). It is reported that inhibition of neddylation repressed NF-κB-mediated proinflammatory cytokine production in macrophages. However, the role of neddylation in the proliferation and survival of macrophages has not been well defined. Here we report that partial inactivation of the neddylation pathway by a specific Nedd8-activating enzyme E1 (NAE) inhibitor MLN4924 reduced LPS-induced production of the proinflammatory cytokines TNF-α and IL-6 without obvious impairment of cell viability. However, persistent and severe inactivation of neddylation by MLN4924 significantly inhibited cell proliferation by inducing G2 phase cell-cycle arrest and further triggered cell death by inducing apoptosis in RAW264.7 macrophages. Mechanistic analysis revealed that inactivation of neddylation blocked cullin neddylation, inhibited CRL E3 ligase activity, and thus led to the accumulation of CRL substrates, resulting in cell-cycle arrest, DNA damage response and apoptosis. The findings revealed that neddylation serves as an important signaling pathway regulating the proliferation and survival of macrophages.

摘要

类泛素化是一种新的蛋白质翻译后修饰方式,它将类泛素分子 Nedd8 添加到靶蛋白上。已鉴定的类泛素化靶标是 cullins,它们作为 Cullin-RING E3 连接酶(CRL)的必需组成部分。据报道,抑制类泛素化可抑制巨噬细胞中 NF-κB 介导的促炎细胞因子产生。然而,类泛素化在巨噬细胞增殖和存活中的作用尚未得到很好的定义。在这里,我们报告说,通过特异性 Nedd8-激活酶 E1(NAE)抑制剂 MLN4924 部分失活类泛素化途径可减少 LPS 诱导的促炎细胞因子 TNF-α 和 IL-6 的产生,而对细胞活力没有明显损害。然而,MLN4924 持续且严重地失活类泛素化会通过诱导 G2 期细胞周期停滞显著抑制细胞增殖,并通过诱导 RAW264.7 巨噬细胞凋亡进一步引发细胞死亡。机制分析表明,类泛素化失活会阻断 cullin 类泛素化,抑制 CRL E3 连接酶活性,从而导致 CRL 底物积累,导致细胞周期停滞、DNA 损伤反应和细胞凋亡。这些发现表明,类泛素化作为调节巨噬细胞增殖和存活的重要信号通路。

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