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首页> 外文期刊>Chemical research in toxicology >Polybrominated Diphenyl Ethers Quinone Induces NCOA4-Mediated Ferritinophagy through Selectively Autophagic Degradation of Ferritin
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Polybrominated Diphenyl Ethers Quinone Induces NCOA4-Mediated Ferritinophagy through Selectively Autophagic Degradation of Ferritin

机译:聚溴二苯基醚醌通过选择性自噬降解铁蛋白的自噬降诱导NCOA4介导的铁陶氏体

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Polybrominated diphenyl ethers (PBDEs) have been detected ubiquitously in biological and environmental samples. Growing epidemiological data suggested the obvious correlation of PBDEs exposure with adverse health outcomes toward human beings, but exact molecular mechanism(s) are limited. Especially, the toxicological information regarding PBDEs metabolites is missing. Thereafter, this study intends to explore unidentified cell death modalities caused by PBDEs reactive quinone-type metabolite, PBDEQ We found that PBDEQ induces autophagy in an ROS-dependent manner. Interestingly, the results indicated that PBDEQ degraded ferritin and activated a selective autophagy (termed as ferritinophagy) by using NCOA4 as its cargo receptor. These processes may further promote the release of iron and ROS. These results suggested the incidence of ferritinophagy induced by PBDEQ, which may contribute to PBDE exposure-caused diseases and dysfunctions.
机译:在生物和环境样品中普遍检测到多溴二苯醚(PBDES)。 生长流行病学数据表明,PBDE对人类不良健康结果的明显相关性,但确切的分子机制有限。 特别是,缺少有关PBDES代谢物的毒理学信息。 此后,本研究旨在探讨由PBDES反应性醌型代谢物,PBDEQ引起的未识别的细胞死亡方式,我们发现PBDEQ以依赖于ROS依赖性的方式诱导自噬。 有趣的是,结果表明,PBDEQ降解铁蛋白并通过使用NCOA4作为其货物受体激活选择性自噬(称为铁纤维)。 这些过程可以进一步促进铁和RO的释放。 这些结果表明,PBDEQ诱导的铁纤维发病率,这可能有助于PBDE暴露导致的疾病和功能障碍。

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