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Changes in proteomic profiles in different prostate lobes of male rats throughout growth and development and aging stages of the life span

机译:在整个生命的生长,发育和衰老阶段,雄性大鼠不同前列腺小叶蛋白质组学特征的变化

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BACKGROUND Aging-related changes in important cellular pathways in the prostate may promote a permissive environment for an increased risk for prostatic disease development such as prostate cancer. Our objectives were to examine for such changes, by systematically determining the effects of growth and development and aging on proteomic profiles in different lobes of the rat prostate. METHODS Prostate lobes (dorsolateral lobe, DL and ventral lobe, VL) were obtained from male Fisher rats of various ages representing young (4 months), mature (12 months), old (18 months), and very old (24 months). Differentially expressed proteins between age groups in each lobe were identified using a proteomic approach, isobaric Tags for Relative and Absolute Quantitation (iTRAQ). Select changes in the DL and VL were verified by immunoblot analysis. RESULTS iTRAQ identified 317 proteins with high confidence. iTRAQ discovered 12 and 6 proteins significantly modulated in response to growth and development in the DL and VL, respectively, and 42 and 29 proteins significantly modulated in response to aging in the DL and VL, respectively. Proteins modulated during growth and development in the DL and VL are involved in a variety of biological processes including cell communication and development, whereas proteins modulated during aging were predominantly related to antioxidant activity and immunity. Immunoblot analysis verified age-related changes for ??-1 antitrypsin, annexin A1, hypoxia up-regulated protein 1, and 78 kDa glucose-regulated protein. CONCLUSIONS Aging results in changes in numerous prostatic proteins and pathways which are mainly linked to inflammation and may lead to prostatic disease development. Prostate 73: 363-375, 2013. ? 2012 Wiley Periodicals, Inc.
机译:背景技术前列腺中重要细胞途径中与衰老相关的变化可以促进宽松的环境,从而增加前列腺疾病发展的风险,例如前列腺癌。我们的目标是通过系统地确定生长,发育和衰老对大鼠前列腺不同叶中蛋白质组学特征的影响,来检查此类变化。方法从不同年龄的雄性费舍尔雄性大鼠(分别为年轻(4个月),成熟(12个月),大龄(18个月)和非常大(24个月)的雄性费舍尔大鼠获得前列腺小叶(背外侧叶,DL和腹叶,VL)。使用蛋白质组学方法(相对定量和绝对定量的同量异位标签(iTRAQ))鉴定每个叶的年龄组之间差异表达的蛋白质。通过免疫印迹分析验证了DL和VL中的选择变化。结果iTRAQ高可信度鉴定出317种蛋白质。 iTRAQ发现分别响应于DL和VL中的生长和发育而被显着调节的12和6个蛋白,以及响应于DL和VL中的衰老而被显着调节的42和29个蛋白。在DL和VL的生长和发育过程中调节的蛋白质参与多种生物学过程,包括细胞通讯和发育,而在衰老过程中调节的蛋白质主要与抗氧化剂活性和免疫力有关。免疫印迹分析证实了??-1抗胰蛋白酶,膜联蛋白A1,缺氧上调蛋白1和78 kDa葡萄糖调节蛋白的年龄相关变化。结论衰老导致许多前列腺蛋白和途径的变化,这些变化主要与炎症有关,并可能导致前列腺疾病的发展。前列腺73:363-375,2013年。 2012 Wiley期刊公司

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