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Cell cycle arrest evidence, parasiticidal and bactericidal properties induced by L-amino acid oxidase from Bothrops atrox snake venom

机译:rop蛇毒中L-氨基酸氧化酶诱导的细胞周期阻滞证据,杀虫和杀菌特性

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摘要

The present article describes an L-amino acid oxidase from Bothrops atrox snake venom as with antiprotozoal activities in Trypanosoma cruzi and in different species of Leishmania (Leishmania braziliensis, Leishmania donovani and Leishmania major). Leishmanicidal effects were inhibited by catalase, suggesting that they are mediated by H2O2 production. Leishmania spp. cause a spectrum of diseases, ranging from self-healing ulcers to disseminated and often fatal infections, depending on the species involved and the host's immune response. BatroxLAAO also displays bactericidal activity against both Gram-positive and Gram-negative bacteria. The apoptosis induced by BatroxLAAO on HL-60 cell lines and PBMC cells was determined by morphological cell evaluation using a mix of fluorescent dyes. As revealed by flow cytometry analysis, suppression of cell proliferation with BatroxLAAO was accompanied by the significant accumulation of cells in the G0/G1 phase boundary in HL-60 cells. BatroxLAAO at 25 mu g/mL and 50 mu g/mL blocked G0-G1 transition, resulting in G0/G1 phase cell cycle arrest, thereby delaying the progression of cells through S and G2/M phase in HL-60 cells. This was shown by an accentuated decrease in the proportion of cells in S phase, and the almost absence of G2/M phase cell population. BatroxLAAO is an interesting enzyme that provides a better understanding of the ophidian envenomation mechanism, and has biotechnological potential as a model for therapeutic agents. (C) 2011 Elsevier Masson SAS. All rights reserved.
机译:本文介绍了一种来自拟南芥(Bothrops atrox)蛇毒的L-氨基酸氧化酶,在克鲁斯锥虫和利什曼原虫(Leishmania braziliensis,Leishmania donovani和Leishmania major)的不同物种中具有抗原生动物活性。过氧化氢酶抑制了杀菌作用,表明它们是由过氧化氢的产生介导的。利什曼原虫属根据涉及的物种和宿主的免疫反应,会导致一系列疾病,从自我修复的溃疡到弥漫性甚至致命的感染。 BatroxLAAO还显示出对革兰氏阳性和革兰氏阴性细菌的杀菌活性。 BatroxLAAO诱导的HL-60细胞系和PBMC细胞凋亡是通过使用荧光染料混合物进行形态学细胞评估来确定的。如流式细胞仪分析所揭示的那样,BatroxLAAO对细胞增殖的抑制伴随着HL-60细胞在G0 / G1相界中的大量细胞聚集。在25μg / mL和50μg / mL的BatroxLAAO阻断G0-G1过渡,导致G0 / G1期细胞周期停滞,从而延迟HL-60细胞通过S和G2 / M期的细胞进程。通过S期细胞比例的明显降低和几乎没有G2 / M期细胞群体的表现,可以看出这一点。 BatroxLAAO是一种有趣的酶,可更好地理解ophidian的毒化机制,并具有作为治疗剂模型的生物技术潜力。 (C)2011 Elsevier Masson SAS。版权所有。

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