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p53 Mediates Colistin-Induced Autophagy and Apoptosis in PC-12 Cells

机译:p53介导colistin诱导的PC-12细胞自噬和凋亡。

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摘要

The mechanism of colistin-induced neurotoxicity is still unknown. Our recent study (L.Zhang,Y.H.Zhao,W.J. Ding,G.Z. Jiang, Z.Y. Lu, L. Li, J. L. Wang, J.Li, and J.C. Li, Antimicrob Agents Chemother 59:2189-2197, 2015, http://dx.doi.org/10.1128/AAC.04092-14; H. Jiang, J. C. Li,T.Zhou, C. H. Wang, H. Zhang, and H. Wang, Int J Mol Med 33: 1298-1304, 2014, http://dx.doi.org/10.3892/ijmm. 2014.1684) indicates that colistin induces autophagy and apoptosis in rat adrenal medulla PC-12 cells, and there is interplay between both cellular events. As an important cellular stress sensor, phosphoprotein p53 can trigger cell cycle arrest and apoptosis and regulate autophagy. The aim of the present study was to investigate the involvement of the p53 pathway in colistin-induced neurotoxicity in PC-12 cells. Specifically, cells were treated with colistin (125 mu g/ml) in the absence and presence of a p53 inhibitor, pifithrin-alpha(PFT- alpha; 20 nM), for 12 h and 24 h, and the typical hallmarks of autophagy and apoptosis were examined by fluorescence/immunofluorescence microscopy and electron microscopy, real-time PCR, and Western blotting. The results indicate that colistin had a stimulatory effect on the expression levels of the target genes and proteins involved in autophagy and apoptosis, including LC3-II/ I, p53, DRAM (damage-regulated autophagy modulator), PUMA (p53 upregulated modulator of apoptosis), Bax, p-AMPK (activated form of AMP-activated protein kinase), and caspase-3. In contrast,colistin appeared to have an inhibitory effect on the expression of p-mTOR (activated form of mammalian target of rapamycin), which is another target protein in autophagy. Importantly, analysis of the levels of p53 in the cells treated with colistin revealed an increase in nuclear p53 at 12 h and cytoplasmic p53 at 24 h. Pretreatment of colistin-treated cells with PFT-alpha inhibited autophagy and promoted colistin-induced apoptosis. This is the first study to demonstrate that colistin-induced autophagy and apoptosis are associated with the p53-mediated pathway.
机译:大肠菌素诱导的神经毒性的机制仍是未知的。我们最近的研究(Zhang Zhang,YHZhao,DW Ding,Jiang GZ Jiang,Lu ZY Li,Li,JL Wang,J.Li,and JC Li,Antimicrob Agents Chemother 59:2189-2197,2015,http:// dx.doi.org/10.1128/AAC.04092-14;姜江,李建春,周T,王春,张宏,王泓,国际分子医学杂志33:1298-1304,2014,http ://dx.doi.org/10.3892/ijmm.2014.1684)表明大肠菌素在大鼠肾上腺髓质PC-12细胞中诱导自噬和凋亡,并且两种细胞事件之间存在相互作用。作为重要的细胞应激传感器,磷蛋白p53可以触发细胞周期停滞和凋亡并调节自噬。本研究的目的是研究p53途径在大肠菌素诱导的PC-12细胞神经毒性中的作用。具体而言,在不存在和存在p53抑制剂pifithrin-alpha(PFT-alpha; 20 nM)的情况下,用粘菌素(125μg / ml)处理细胞12 h和24 h,并具有自噬和吞噬的典型特征通过荧光/免疫荧光显微镜和电子显微镜,实时PCR和蛋白质印迹检查细胞凋亡。结果表明大肠粘菌素对涉及自噬和凋亡的靶基因和蛋白质的表达水平具有刺激作用,包括LC3-II / I,p53,DRAM(损伤调节自噬调节剂),PUMA(p53上调凋亡调节剂) ),Bax,p-AMPK(AMP激活的蛋白激酶的激活形式)和caspase-3。相反,colistin似乎对p-mTOR(雷帕霉素哺乳动物靶标的活化形式)的表达具有抑制作用,p-mTOR是自噬中的另一种靶蛋白。重要的是,对大肠菌素处理过的细胞中p53水平的分析表明,在12小时时核p53升高,而在24小时时胞质p53升高。用PFT-α预处理粘菌素处理的细胞可抑制自噬并促进粘菌素诱导的细胞凋亡。这是第一个证明大肠杆菌素诱导的自噬和细胞凋亡与p53介导的途径相关的研究。

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