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时间依赖性肝蛋白质组分析在瘦型和饮食诱导肥胖型小鼠中的应用。

Time-dependent hepatic proteome analysis in lean and diet-induced obese mice.

机构信息

Department of Biotechnology, Daegu University, Kyungsan, Kyungbuk 712-714, Korea.

出版信息

J Microbiol Biotechnol. 2011 Dec;21(12):1211-27. doi: 10.4014/jmb.1107.07056.

Abstract

C57BL/6J mice have been widely used as a diet-induced obesity model because they trigger common features of the human metabolic syndrome. In the present study, C57BL/6J male mice were fed either a high-fat diet (HFD) or normal diet (ND) during a 24-week period, and then the age-dependent liver proteome of mice in two groups was analyzed using 2-DE combined with MALDI-TOF-MS. Among identified proteins, up-regulated proteins were subdivided to early (during the first 4 weeks) and late (20~24 weeks) markers that played a role in diet-induced obesity development. Important early markers included ketohexokinase and prohibitin, and late markers included the 75 kDa glucose-regulated protein, citrate synthase, and selenium-binding liver protein. Of these, the 75 kDa glucoseregulated protein has already been linked to obesity; however, prohibitin protein involved in obesity was identified for the first time in this study. In order to validate the proteomic results and gain insight into metabolic changes between the two groups, we further confirmed the expression pattern of some proteins of interest by Western blot analysis. Combined results of proteomic analysis with Western blot analysis revealed that antioxidant enzymes were progressively decreased, whereas cytoskeletal proteins were time-dependently increased in HFD mice.

摘要

C57BL/6J 小鼠被广泛用作饮食诱导肥胖模型,因为它们会引发人类代谢综合征的常见特征。在本研究中,将雄性 C57BL/6J 小鼠在 24 周的时间内分别用高脂肪饮食(HFD)或正常饮食(ND)喂养,然后使用 2-DE 结合 MALDI-TOF-MS 分析两组小鼠的年龄依赖性肝蛋白质组。在鉴定出的蛋白质中,上调的蛋白质被细分为在饮食诱导肥胖发展中起作用的早期(前 4 周)和晚期(20~24 周)标志物。重要的早期标志物包括酮己糖激酶和抑素,晚期标志物包括 75 kDa 葡萄糖调节蛋白、柠檬酸合酶和硒结合肝蛋白。其中,75 kDa 葡萄糖调节蛋白已与肥胖有关;然而,在这项研究中,首次发现了参与肥胖的抑素蛋白。为了验证蛋白质组学结果并深入了解两组之间的代谢变化,我们还通过 Western blot 分析进一步证实了一些感兴趣蛋白质的表达模式。蛋白质组学分析与 Western blot 分析的综合结果表明,抗氧化酶逐渐减少,而细胞骨架蛋白在 HFD 小鼠中随时间增加。

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