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通过蛋白质印迹分析首次在地中海鲸类皮肤活检组织和培养的成纤维细胞中检测到CYP1A1和CYP2B的诱导。

First detection of CYP1A1 and CYP2B induction in Mediterranean cetacean skin biopsies and cultured fibroblasts by Western blot analysis.

作者信息

Fossi Maria Cristina, Casini Silvia, Bucalossi Daniela, Marsili Letizia

机构信息

Department of Environmental Sciences, Siena University, Via Mattioli 4, Siena, Italy.

出版信息

Mar Environ Res. 2008 Jul;66(1):3-6. doi: 10.1016/j.marenvres.2008.02.006. Epub 2008 Feb 26.

Abstract

The need to develop powerful tools to detect exposure and effects of POPs and emerging contaminants in Mediterranean cetaceans led us to develop a suite of sensitive non-lethal biomarkers in integument biopsies of free-ranging animals. In order to propose induction of CYP1A1 and CYP2B, detected by Western blot analysis, as biomarkers of exposure to OCs, PAHs and PBDEs, a three-phase experimental protocol (in vitro experiments, calibration experiments and field applications) was followed using fibroblast cell cultures and biopsies of Mediterranean Stenella coeruleoalba and Tursiops truncatus. This methodology was confirmed to be sensitive and stable in comparison to previous methods used to detect CYP1A1 in biopsies, enabling analysis of several inducible proteins in non-lethal samples and analysis of material from stranded animals.

摘要

需要开发强大的工具来检测地中海鲸类动物中持久性有机污染物(POPs)和新兴污染物的暴露情况及影响,这促使我们在自由放养动物的皮肤活检中开发一套敏感的非致死性生物标志物。为了将通过蛋白质印迹分析检测到的CYP1A1和CYP2B的诱导作为接触有机氯农药(OCs)、多环芳烃(PAHs)和多溴二苯醚(PBDEs)的生物标志物,我们采用了一个三相实验方案(体外实验、校准实验和现场应用),使用了地中海条纹原海豚(Stenella coeruleoalba)和宽吻海豚(Tursiops truncatus)的成纤维细胞培养物和活检样本。与之前用于检测活检中CYP1A1的方法相比,该方法被证实具有敏感性和稳定性,能够分析非致死样本中的几种可诱导蛋白,并能分析搁浅动物的样本。

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