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首页> 外文期刊>Photochemical & photobiological sciences: the official journal of the European Photochemistry Association and the European Society for Photobiology >Photodynamic therapy with hexyl aminolevulinate induces carbonylation, posttranslational modifications and changed expression of proteins in cell survival and cell death pathways
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Photodynamic therapy with hexyl aminolevulinate induces carbonylation, posttranslational modifications and changed expression of proteins in cell survival and cell death pathways

机译:氨基乙酰丙酸己酯的光动力疗法可诱导羰基化,翻译后修饰以及蛋白质在细胞存活和细胞死亡途径中的表达变化

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摘要

Photodynamic therapy (PDT) using blue light and the potent precursor for protoporphyrin IX, hexyl aminolevulinate (HAL), has been shown to induce apoptosis and necrosis in cancer cells, but the mechanism remains obscure. In the present study, we examined protein carbonylation, expression levels and post-translational modifications in rat bladder cells (AY-27) after PDT with HAL. Altered levels of expression and/or post-translational modifications induced by PDT were observed for numerous proteins, including proteins required for cell mobility, energy supply, cell survival and cell death pathways, by using two-dimensional difference gel electrophoresis (2D-DIGE) and mass spectrometry (MS). Moreover, 10 carbonylated proteins associated with cytoskeleton, transport, oxidative stress response, protein biosynthesis and stability, and DNA repair were identified using immunoprecipitation, two-dimensional gel electrophoresis and MS. Overall, the results indicate that HAL-mediated PDT triggers a complex cellular response involving several biological pathways. Our findings may account for the elucidation of mechanisms modulated by PDT, paving the way to improve clinic PDT-efficacy.
机译:使用蓝光和原卟啉IX的有效前体氨基乙酰丙酸己酯(HAL)进行的光动力疗法(PDT)已显示可诱导癌细胞凋亡和坏死,但该机制仍然不清楚。在本研究中,我们检查了HAL PDT后大鼠膀胱细胞(AY-27)中的蛋白羰基化,表达水平和翻译后修饰。通过使用二维差异凝胶电泳(2D-DIGE),对许多蛋白质(包括细胞移动性,能量供应,细胞存活和细胞死亡途径所需的蛋白质)观察到了由PDT诱导的表达水平和/或翻译后修饰的改变,和质谱(MS)。此外,使用免疫沉淀,二维凝胶电泳和质谱技术鉴定了与细胞骨架,转运,氧化应激反应,蛋白质生物合成和稳定性以及DNA修复相关的10个羰基化蛋白质。总体而言,结果表明,HAL介导的PDT触发了涉及多种生物学途径的复杂细胞反应。我们的发现可能解释了PDT调节的机制,为改善临床PDT效力铺平了道路。

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