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铜纳米颗粒通过PERK-EIF2α-SREBP-1c途径诱导暗纹东方鲀形成脂肪肝。

Copper nanoparticles induce the formation of fatty liver in Takifugu fasciatus triggered by the PERK-EIF2α- SREBP-1c pathway.

作者信息

Wang Tao, Wei Xiaozhen, Sun Yiru, Hu Yadong, Li Jie, Zhang Xinyu, Yin Shaowu, Shi Yonghai, Zhu Yongxiang

机构信息

College of Marine Science and Engineering, Jiangsu Province Engineering Research Center for Aquatic Animals Breeding and Green Efficient Aquacultural Technology, Nanjing Normal University, Nanjing, Jiangsu 210023, China; Co-Innovation Center for Marine Bio-Industry Technology of Jiangsu Province, Lianyungang, Jiangsu 222005, China.

College of Marine Science and Engineering, Jiangsu Province Engineering Research Center for Aquatic Animals Breeding and Green Efficient Aquacultural Technology, Nanjing Normal University, Nanjing, Jiangsu 210023, China; Co-Innovation Center for Marine Bio-Industry Technology of Jiangsu Province, Lianyungang, Jiangsu 222005, China.

出版信息

NanoImpact. 2021 Jan;21:100280. doi: 10.1016/j.impact.2020.100280. Epub 2020 Nov 28.

Abstract

Copper nanoparticles (CuNPs), a new pollutant in water environments, were widely used in various industrial and commercial applications. This study indicated that the presence of CuNPs exposure under environmental related concentration is an inducing factor that contributes to the fatty liver formation in Takifugu fasciatus. Furthermore, we explored the fatty liver formation mechanism. The results shown, (1) the cloned genes related to endoplasmic reticulum stress (ERS) (GRP78, IRE-1α, PERK, and ATF-6α) were highly expressed in the liver of T. fasciatus. (2) after 30-days exposure, CuNPs accumulated in the endoplasmic reticulum of liver and induced the appearance of ERS, then activated unfolded protein response (UPR) signaling pathway. Furthermore, the SREBP-1c pathway that plays a key role in lipid synthesis was activated. (3) by using 4-PBA and GSK inhibitors to respectively stimulate ERS and PKR-like ER kinase (PERK) through in vitro experiments, we confirmed that CuNPs induced the fatty liver formation in T. fasciatus triggered by the PERK-EIF2α pathway by activating the SREBP-1c pathway to promote fatty liver formation. This study provides a new perspective for identifying the pathogens of fatty liver formation, and adds to the knowledge of the ecological safety data service of CuNPs in water.

摘要

铜纳米颗粒(CuNPs)是水环境中的一种新型污染物,广泛应用于各种工业和商业领域。本研究表明,在环境相关浓度下暴露于CuNPs是导致暗纹东方鲀脂肪肝形成的一个诱导因素。此外,我们还探究了脂肪肝的形成机制。结果显示:(1)与内质网应激(ERS)相关的克隆基因(GRP78、IRE-1α、PERK和ATF-6α)在暗纹东方鲀肝脏中高表达。(2)暴露30天后,CuNPs在肝脏内质网中积累,诱导ERS出现,进而激活未折叠蛋白反应(UPR)信号通路。此外,在脂质合成中起关键作用的SREBP-1c通路也被激活。(3)通过体外实验分别用4-PBA和GSK抑制剂刺激ERS和蛋白激酶R样内质网激酶(PERK),我们证实CuNPs通过激活SREBP-1c通路促进脂肪肝形成,从而由PERK-EIF2α通路触发暗纹东方鲀脂肪肝的形成。本研究为确定脂肪肝形成的病原体提供了新的视角,并增加了关于水中CuNPs生态安全数据服务的知识。

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