Finzi Jane K, Chiavegatto Camila W M, Corat Karen F, Lopez Jorge A, Cabrera Odalys G, Mielniczki-Pereira Albanin A, Colli Walter, Alves Maria Júlia M, Gadelha Fernanda R
Departamento de Bioquímica, IB, UNICAMP, Campinas, SP, Brazil.
Mol Biochem Parasitol. 2004 Jan;133(1):37-43. doi: 10.1016/j.molbiopara.2003.08.011.
As an intracellular parasite, Trypanosoma cruzi is exposed to reactive oxygen species. The study of the proteins involved in the hydroperoxide detoxification cascade, tryparedoxin peroxidase included, may lead to the development of a more specific chemotherapy for Chagas'disease. In this work, the involvement of TcCPX in T. cruzi resistance to oxidant-mediated injury was investigated. At low concentrations of hydrogen peroxide cell proliferation was stimulated and parasites increased their resistance to sub-lethal doses of H2O2 (100 microM) if previously treated with a non-toxic concentration of H2O2 (20 microM). Incubation of cells with different H2O2 concentrations induced a dose-dependent increase in TcCPX levels, as detected by Western blotting analysis. The increase in TcCPX levels in the presence of high H2O2 concentrations possibly reflects an initial cell attempt to promote detoxification. To further demonstrate TcCPX involvement in T. cruzi response to oxidative stress, TcCPX overexpressing cells were produced. Compared to pTEX transformed cells, pTEX-TcCPX mutant cells showed a higher mRNA level (129%), without a corresponding increase in protein production (11%), suggesting that regulation of gene expression occurs at post-transcriptional levels. Furthermore, parasite treatment with 200 microM H2O2 for 30 min, led to an increase in mRNA (192%), but not in protein levels (24%). Higher mRNA levels correlated to protein levels were observed only after longer H2O2 incubation periods (1-2 h), suggesting that protein translation occurs accordingly to parasite needs. An increase in glucose-6-phosphate dehydrogenase activity was observed in pTEX-TcCPX epimastigotes that could provide cells with extra reducing power and a higher growth index.
作为一种细胞内寄生虫,克氏锥虫会暴露于活性氧物质中。对参与氢过氧化物解毒级联反应的蛋白质(包括锥虫硫氧还蛋白过氧化物酶)的研究,可能会促成针对恰加斯病的更具特异性的化疗方法的开发。在这项研究中,对锥虫CPX(TcCPX)在克氏锥虫抵抗氧化介导损伤中的作用进行了调查。在低浓度过氧化氢条件下,细胞增殖受到刺激,并且如果先用无毒浓度的过氧化氢(20微摩尔)处理过,寄生虫对亚致死剂量的H2O2(100微摩尔)的抗性会增强。通过蛋白质印迹分析检测发现,用不同浓度的H2O2孵育细胞会导致TcCPX水平呈剂量依赖性增加。在高浓度H2O2存在的情况下,TcCPX水平的增加可能反映了细胞促进解毒的初步尝试。为了进一步证明TcCPX参与克氏锥虫对氧化应激的反应,构建了过表达TcCPX的细胞。与pTEX转化细胞相比,pTEX-TcCPX突变细胞显示出更高的mRNA水平(129%),但蛋白质产量没有相应增加(11%),这表明基因表达的调控发生在转录后水平。此外,用浓度为200微摩尔的H2O2处理寄生虫30分钟,会导致mRNA增加(192%),但蛋白质水平没有增加(24%)。仅在较长时间的H2O2孵育期(1 - 2小时)后,才观察到与蛋白质水平相关的更高mRNA水平,这表明蛋白质翻译是根据寄生虫的需求进行的。在pTEX-TcCPX型前鞭毛体中观察到葡萄糖-6-磷酸脱氢酶活性增加,这可以为细胞提供额外的还原能力和更高的生长指数。