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首页> 外文期刊>Scientific reports. >Proteomic evidences for microcystin-RR-induced toxicological alterations in mice liver
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Proteomic evidences for microcystin-RR-induced toxicological alterations in mice liver

机译:微囊藻毒素-RR引起的小鼠肝脏毒理学改变的蛋白质组学证据

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摘要

This study deals with the isolation and purification of an important variant of microcystins namely microcystin-RR (MCYST-RR) from Microcystis aeruginosa and reports its effects on mice liver protein profile and cellular functions. Protein profiling by 2-dimensional gel electrophoresis revealed changes in the number and accumulation of protein spots in liver of mice treated with different concentrations of MCYST-RR. Untreated (control) mice liver showed 368 protein spots while the number was 355, 348 and 332 in liver of mice treated with 200, 300 and 400?μg?kg body wt?1 of MCYST-RR respectively. Altogether 102, 97, and 92 spots were differentially up-accumulated and 93, 91, and 87 spots were down- accumulated respectively with the treatment of 200, 300, 400?μg?kg body wt?1. Eighteen differentially accumulated proteins present in all the four conditions were identified by MALDI-TOF MS. Of these eighteen proteins, 12 appeared to be involved in apoptosis/toxicological manifestations. Pathway analysis by Reactome and PANTHER database also mapped the identified proteins to programmed cell death/apoptosis clade. That MCYST-RR induces apoptosis in liver tissues was also confirmed by DNA fragmentation assay. Results of this study elucidate the proteomic basis for the hepatotoxicity of MCYST-RR which is otherwise poorly understood till date.
机译:这项研究涉及从铜绿微囊藻的微囊藻毒素的重要变体即微囊藻毒素-RR(MCYST-RR)的分离和纯化,并报道其对小鼠肝脏蛋白谱和细胞功能的影响。通过二维凝胶电泳进行的蛋白质谱分析揭示了用不同浓度的MCYST-RR处理的小鼠肝脏中蛋白质斑点的数量和积累的变化。未经处理(对照)的小鼠肝脏显示368个蛋白斑点,而分别用200、300和400μg/ kg体重的MCYST-RR处理的小鼠肝脏中的蛋白斑点分别为355、348和332。分别处理200、300、400μg·kg·kg·kg-1体重时,分别累积了102、97和92个斑点,分别减少了93、91和87个斑点。通过MALDI-TOF MS鉴定了在所有四个条件下均存在的18种差异积累的蛋白质。在这18种蛋白质中,有12种似乎与细胞凋亡/毒理学表现有关。通过Reactome和PANTHER数据库进行的途径分析也将鉴定出的蛋白质映射到程序化的细胞死亡/凋亡进化枝。 DNA片段分析也证实了MCYST-RR诱导肝组织凋亡。这项研究的结果阐明了MCYST-RR肝毒性的蛋白质组学基础,迄今为止,人们对它的了解还很少。

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