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SOD2 通过 lncRNA CLCA3p 促进 ABCC2 的表达,提高肝细胞的解毒能力。

SOD2 promotes the expression of ABCC2 through lncRNA CLCA3p and improves the detoxification capability of liver cells.

机构信息

Department of Hepatobiliary Surgery and Fujian Institute of Hepatobiliary Surgery, Fujian Medical University Union Hospital, Fuzhou, China.

Department of Hepatobiliary Surgery and Fujian Institute of Hepatobiliary Surgery, Fujian Medical University Union Hospital, Fuzhou, China; Key Laboratory of Ministry of Education for Gastrointestinal Cancer, Research Center for Molecular Medicine, Fujian Medical University, Fuzhou, China.

出版信息

Toxicol Lett. 2020 Jul 1;327:9-18. doi: 10.1016/j.toxlet.2020.03.013. Epub 2020 Mar 20.

Abstract

Superoxide dismutase 2 (SOD2) is a key enzyme for scavenging reactive oxygen species produced by mitochondria, which plays an important role in maintaining cellular homeostasis. However, its effects on the detoxification capability of liver cells have not been reported. In this study, we found that change in SOD2 expression affects the proliferation of liver cells. Genome-wide microarray analysis showed that SOD2 positively regulates the drug transporter ABCC2, and co-expression analysis suggested that lncRNA CLCA3P participates in the process. Further experiments showed that SOD2 can promote the expression of CLCA3P, which increases the transcription of ABCC2 by interacting with the transcription factor IRF1. By increasing ABCC2 expression SOD2 facilitates drugs efflux of liver cells and thus promotes their survival under a drug-toxic environment. This study elucidates the improvement of the detoxification of liver cells by a regulatory axis, SOD2-CLCA3P-IRF1-ABCC2, and provides novel insight into the modification of human liver cells that can be applied to bioartificial liver system or the study of SOD2 in drug metabolism.

摘要

超氧化物歧化酶 2(SOD2)是一种清除线粒体产生的活性氧的关键酶,在维持细胞内稳态方面发挥着重要作用。然而,其对肝细胞解毒能力的影响尚未有报道。在本研究中,我们发现 SOD2 表达的改变影响了肝细胞的增殖。全基因组微阵列分析显示,SOD2 正向调节药物转运体 ABCC2,共表达分析表明 lncRNA CLCA3P 参与了这一过程。进一步的实验表明,SOD2 可以促进 CLCA3P 的表达,通过与转录因子 IRF1 相互作用增加 ABCC2 的转录。通过增加 ABCC2 的表达,SOD2 促进了肝细胞内药物的外排,从而促进了它们在药物毒性环境下的存活。本研究阐明了 SOD2-CLCA3P-IRF1-ABCC2 调控轴对肝细胞解毒能力的改善,并为应用于生物人工肝脏系统或 SOD2 在药物代谢研究中的人类肝细胞修饰提供了新的见解。

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