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首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >Effects of minimally toxic levels of carbonyl cyanide P-(trifluoromethoxy) phenylhydrazone (FCCP), elucidated through differential gene expression with biochemical and morphological correlations.
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Effects of minimally toxic levels of carbonyl cyanide P-(trifluoromethoxy) phenylhydrazone (FCCP), elucidated through differential gene expression with biochemical and morphological correlations.

机译:通过差异基因表达与生物化学和形态学关联阐明了羰基氰化物P-(三氟甲氧基)苯hydr(FCCP)的最低毒性水平的影响。

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Uncouplers of oxidative phosphorylation have relevance to bioenergetics and obesity. The mechanisms of action of chemical uncouplers of oxidative phosphorylation on biological systems were evaluated using differential gene expression. The transcriptional response in human rhabdomyosarcoma cell line (RD), was elucidated following treatment with carbonyl cyanide p-(trifluoromethoxy) phenylhydrazone (FCCP), a classical uncoupling agent. Changes in mitochondrial membrane potential were used as the biological dosimeter. There was an increase in membrane depolarization with increasing concentrations of FCCP. The concentration at 75% uncoupling (20 microM) was chosen to study gene expression changes, using cDNA-based large-scale differential gene expression (LSDGE) platforms. At the above concentration, subtle light microscopic and clear gene expression changes were observed at 1, 2, and 10 h. Statistically significant transcriptional changes were largely associated with protein synthesis, cell cycle regulation, cytoskeletal proteins, energy metabolism, apoptosis, and inflammatory mediators. Bromodeoxyuridine (BrdU) and propidium iodide (PI) assays revealed cell cycle arrest to occur in the G1 and S phases. There was a significant initial decrease in the intracellular adenosine triphosphate (ATP) concentrations. The following seven genes were selected as potential molecular markers for chemical uncouplers: seryl-tRNA synthetase (Ser-tRS), glutamine-hydrolyzing asparagine synthetase (Glut-HAS), mitochondrial bifunctional methylenetetrahydrofolate dehydrogenase (Mit BMD), mitochondrial heat shock 10-kDa protein (Mit HSP 10), proliferating cyclic nuclear antigen (PCNA), cytoplasmic beta-actin (Act B), and growth arrest and DNA damage-inducible protein 153 (GADD153). Transcriptional changes of all seven genes were later confirmed with reverse transcription-polymerase chain reaction (RT-PCR). These results suggest that gene expression changes may provide a sensitive indicator of uncoupling in response to chemical exposure.
机译:氧化磷酸化的解偶联剂与生物能和肥胖症有关。使用差异基因表达评估了氧化磷酸化化学解偶联剂对生物系统的作用机理。在用经典的去偶联剂羰基氰对-(三氟甲氧基)苯基hydr(FCCP)处理后,阐明了人横纹肌肉瘤细胞系(RD)中的转录反应。线粒体膜电位的变化用作生物剂量计。随着FCCP浓度的增加,膜去极化也增加。使用基于cDNA的大规模差异基因表达(LSDGE)平台,选择75%解偶联浓度(20 microM)来研究基因表达变化。在上述浓度下,在1、2和10 h观察到微妙的光学显微镜和清晰的基因表达变化。统计学上显着的转录变化主要与蛋白质合成,细胞周期调节,细胞骨架蛋白质,能量代谢,细胞凋亡和炎症介质有关。溴脱氧尿苷(BrdU)和碘化丙啶(PI)分析显示细胞周期停滞发生在G1和S期。胞内三磷酸腺苷(ATP)浓度显着开始下降。选择以下七个基因作为化学解偶联剂的潜在分子标记:丝氨酰tRNA合成酶(Ser-tRS),谷氨酰胺水解天冬酰胺合成酶(Glut-HAS),线粒体双功能亚甲基四氢叶酸脱氢酶(Mit BMD),线粒体热休克10-kDa蛋白质(Mit HSP 10),增殖环核抗原(PCNA),细胞质β-肌动蛋白(Act B)以及生长停滞和DNA损伤诱导蛋白153(GADD153)。后来通过逆转录聚合酶链反应(RT-PCR)证实了所有七个基因的转录变化。这些结果表明基因表达的变化可能提供一个敏感的指标,表明对化学暴露的解偶联。

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