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

机译:P53在PC-12细胞中介导Colistin诱导的自噬和细胞凋亡

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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:Colistin诱导的神经毒性的机制仍然未知。我们最近的研究(L.Zhang,Yhzhao,WJ叮,GZ Jiang,Zy Lu,L.Li,JL Wang,J.Li和JC Li,Antimicrob Agents Chemother 59:2189-2197,2015,http:// dx.doi.org/10.1128/AAC.04092-14; H.江,JC Li,T.U,Ch Wang,H. Zhang,H. Wang,Int J Mol Med 33:1298-1304,2014,HTTP ://dx.doi.org/10.3892/ijmm。2014.1684)表明Colistin在大鼠肾上腺Medulla 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。作为一种重要的细胞应激传感器,磷蛋白P53可以引发细胞周期停滞和细胞凋亡并调节自噬。本研究的目的是探讨P53途径在COLISTIN诱导的PC-12细胞中的神经毒性中的参与。具体地,在P53抑制剂的不存在和存在下用Colistin(125μg/ ml)处理细胞,P53抑制剂(PFT-alpha; 20nm),12小时和24小时,以及自噬的典型标志和通过荧光/免疫荧光显微镜和电子显微镜,实时PCR和Western印迹检查细胞凋亡。结果表明,Colistin对靶基因和蛋白质的表达水平具有诱导效应,所述靶基因和凋亡所述的靶基因和凋亡,包括LC3-II / I,P53,DRAM(损伤调节的自噬调节剂),PUMA(P53上调调节剂的细胞凋亡),Bax,P-AMPK(激活形式的AMP-活化蛋白激酶)和Caspase-3。相比之下,Colistin似乎对p-mTOR的表达(雷帕霉素的活化形式的哺乳动物靶标)的表达具有抑制作用,这是自噬中的另一种靶蛋白。重要的是,分析用Colistin处理的细胞中P53水平显示在12小时和24小时的细胞质P53时显示核P53的增加。用PFT-α的药物处理细胞的预处理抑制自噬并促进Colistin诱导的细胞凋亡。这是第一次证明Colistin诱导的自噬和细胞凋亡与P53介导的途径有关的研究。

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    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Monash Univ Monash Inst Pharmaceut Sci Drug Delivery Disposit &

    Dynam Parkville Vic Australia;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Jinzhou Med Univ Inst Anim Husb &

    Vet Med Jinzhou Liaoning Peoples R China;

    Jinzhou Med Univ Inst Anim Husb &

    Vet Med Jinzhou Liaoning Peoples R China;

    Jinzhou Med Univ Inst Anim Husb &

    Vet Med Jinzhou Liaoning Peoples R China;

    Jinzhou Med Univ Inst Anim Husb &

    Vet Med Jinzhou Liaoning Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

    Monash Univ Monash Inst Pharmaceut Sci Drug Delivery Disposit &

    Dynam Parkville Vic Australia;

    Northeast Agr Univ Coll Vet Med Harbin Peoples R China;

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  • 正文语种 eng
  • 中图分类 治疗学;
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