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多氟和全氟化合物激活人类孕烷X受体。

Poly- and perfluorinated compounds activate human pregnane X receptor.

作者信息

Zhang Yi-Ming, Dong Xiao-Yu, Fan Li-Juan, Zhang Zhi-Lei, Wang Qian, Jiang Nan, Yang Xu-Shu

机构信息

School of Basic Medical Sciences, Nanjing Medical University, Nanjing 211166, China.

School of Basic Medical Sciences, Nanjing Medical University, Nanjing 211166, China.

出版信息

Toxicology. 2017 Apr 1;380:23-29. doi: 10.1016/j.tox.2017.01.012. Epub 2017 Jan 20.

Abstract

Poly- and perfluorinated compounds (PFCs), which have been detected worldwide in human blood, surface water and house dust, are suspected to induce potential endocrine-disrupting hormonal effects. In this study, cell-based reporter gene assays were used to determine the activity of a variety of PFCs against the human pregnane X receptor (hPXR) to identify the critical structural feature of PFCs related to their hPXR activity. Molecular docking studies combined with site-directed mutagenesis were employed to investigate the mechanism by which PFCs interact with and activate hPXR. We found that all tested PFCs can activate hPXR. The hPXR activity of the PFCs correlates with the carbon chain length and the functional group of the chemicals. Hydrogen bonding was characteristic of the interaction between PFCs and hPXR. We also identified the key residues within the hPXR ligand-binding pocket responsible for PFC-hPXR interaction. The outcome of the present study threw a light on the mechanism by which PFCs activate hPXR. PFCs may pose some potential endocrine-disrupting hormonal effects via activation of hPXR.

摘要

全氟和多氟化合物(PFCs)在全球范围内的人体血液、地表水和室内灰尘中均有检测到,人们怀疑它们会引发潜在的内分泌干扰激素效应。在本研究中,基于细胞的报告基因检测被用于测定多种PFCs对人孕烷X受体(hPXR)的活性,以确定与hPXR活性相关的PFCs的关键结构特征。采用分子对接研究结合定点诱变来探究PFCs与hPXR相互作用并激活hPXR的机制。我们发现,所有测试的PFCs均可激活hPXR。PFCs的hPXR活性与化学物质的碳链长度和官能团相关。氢键是PFCs与hPXR相互作用的特征。我们还确定了hPXR配体结合口袋内负责PFC-hPXR相互作用的关键残基。本研究结果揭示了PFCs激活hPXR的机制。PFCs可能通过激活hPXR产生一些潜在的内分泌干扰激素效应。

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