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大鼠暴露于肝癌致癌物美吡拉敏后肝脏蛋白质修饰和表达的剂量反应

Dose-responses in rat hepatic protein modification and expression following exposure to the rat hepatocarcinogen methapyrilene.

作者信息

Richardson F C, Horn D M, Anderson N L

机构信息

Toxicology Research Laboratories, Lilly Research Laboratories, Greenfield, IN.

出版信息

Carcinogenesis. 1994 Feb;15(2):325-9. doi: 10.1093/carcin/15.2.325.

DOI:10.1093/carcin/15.2.325
PMID:8313526
Abstract

Dose-related effects of methapyrilene (MP) on protein modification and expression were examined using two-dimensional gel electrophoresis (2-D PAGE) coupled with computer analysis. Methapyrilene was administered ad libitum at doses of 0, 62.5, 125, 250 and 1000 p.p.m. to male F-344 rats for 12 weeks beginning at 8 weeks of age. Following treatment, livers were removed and frozen for 2-D PAGE analysis. Separation of hepatic proteins was conducted using ISO-DALT technology. Changes in abundance and modification of hepatic proteins were determined using the Kepler software package. Covalent modifications of three specific mitochondrial proteins were quantified using a charge modification index. Dose-response relationships were analyzed using Tukey's trend test. Results demonstrated that covalent modification of the three mitochondrial proteins was linearly related to dose and that a dose effect could be found at all dose levels in 2 out of 3 proteins. Two forms of change in protein expression were observed: (i) a dose-dependent change with effects at all doses and (ii) a change only at the toxic dose of 1000 p.p.m. MP. These results demonstrate a molecular effect of MP at doses that do not produce cellular responses including toxicity or increases in cell replication suggesting that these specific mitochondrial modifications are molecular dosimeters but are probably not direct factors and/or sufficient factors in carcinogenesis. This study also demonstrates the potential use of 2-D PAGE electrophoresis to delineate the effect of dose on expression of specific proteins.

摘要

采用二维凝胶电泳(2-D PAGE)结合计算机分析,研究了甲吡咯啉(MP)对蛋白质修饰和表达的剂量相关效应。从8周龄开始,以0、62.5、125、250和1000 ppm的剂量随意给雄性F-344大鼠喂食甲吡咯啉,持续12周。处理后,取出肝脏并冷冻用于二维凝胶电泳分析。使用ISO-DALT技术分离肝脏蛋白质。使用开普勒软件包确定肝脏蛋白质丰度和修饰的变化。使用电荷修饰指数对三种特定线粒体蛋白质的共价修饰进行定量。使用Tukey趋势检验分析剂量反应关系。结果表明,三种线粒体蛋白质的共价修饰与剂量呈线性相关,并且在3种蛋白质中的2种蛋白质的所有剂量水平上都能发现剂量效应。观察到蛋白质表达的两种变化形式:(i)所有剂量下均有影响的剂量依赖性变化,以及(ii)仅在1000 ppm MP的毒性剂量下出现的变化。这些结果表明,MP在不产生包括毒性或细胞复制增加在内的细胞反应的剂量下具有分子效应,这表明这些特定的线粒体修饰是分子剂量计,但可能不是致癌作用的直接因素和/或充分因素。本研究还证明了二维凝胶电泳在描绘剂量对特定蛋白质表达影响方面的潜在用途。

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Dose-responses in rat hepatic protein modification and expression following exposure to the rat hepatocarcinogen methapyrilene.大鼠暴露于肝癌致癌物美吡拉敏后肝脏蛋白质修饰和表达的剂量反应
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2
Covalent protein modifications and gene expression changes in rodent liver following administration of methapyrilene: a study using two-dimensional electrophoresis.
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Editor's Highlight: Organ-Specific Epigenetic Changes Induced by the Nongenotoxic Liver Carcinogen Methapyrilene in Fischer 344 Rats.编辑推荐:非遗传毒性肝致癌物甲吡咯烷在Fischer 344大鼠中诱导的器官特异性表观遗传变化。
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Comparisons of protein changes in human and rodent hepatocytes induced by the rat-specific carcinogen, methapyrilene.
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Effect of methapyrilene hydrochloride on hepatic intracellular iron metabolism in vivo and in vitro.盐酸甲基吡咯啉对体内外肝脏细胞内铁代谢的影响。
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Effects of methapyrilene on DNA synthesis in mice and rats following continuous dietary exposure.连续经口摄入后,甲苯吡咯对小鼠和大鼠DNA合成的影响。
Carcinogenesis. 1992 Dec;13(12):2453-7. doi: 10.1093/carcin/13.12.2453.

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