1. Academic Validation
  2. α-amanitin induces autophagy through AMPK-mTOR-ULK1 signaling pathway in hepatocytes

α-amanitin induces autophagy through AMPK-mTOR-ULK1 signaling pathway in hepatocytes

  • Toxicol Lett. 2023 Jun 15;S0378-4274(23)00204-7. doi: 10.1016/j.toxlet.2023.06.004.
Yue Xu 1 Shangwen Wang 1 Chi-Kwan Leung 2 Hao Chen 1 Chan Wang 1 Huijie Zhang 1 Shuwei Zhang 1 Yi Tan 1 Haowei Wang 1 Lin Miao 1 Yi Li 1 Yizhen Huang 1 Xiaoxing Zhang 1 Genmeng Yang 3 Ruilin Zhang 4 Xiaofeng Zeng 5
Affiliations

Affiliations

  • 1 Department of Forensic Medicine, School of Forensic Medicine, Kunming Medical University, Kunming, China.
  • 2 School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong; CUHK-SDU Joint Laboratory of Reproductive Genetics, School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.
  • 3 Department of Forensic Medicine, School of Forensic Medicine, Kunming Medical University, Kunming, China. Electronic address: 1223984885@qq.com.
  • 4 Department of Forensic Medicine, School of Forensic Medicine, Kunming Medical University, Kunming, China. Electronic address: zrlorg@126.com.
  • 5 Department of Forensic Medicine, School of Forensic Medicine, Kunming Medical University, Kunming, China. Electronic address: zxf2004033@163.com.
Abstract

Amanitin poisoning is one of the most life-threatening mushroom poisonings. α-Amanitin plays a key role in Amanita phalloides intoxication. α-Amanitin shows toxic effects on the liver. However, the mechanism by which α-amanitin induces liver injury has not been elucidated. Autophagy plays a crucial role in maintaining cellular homeostasis and is closely related to the occurrence of a variety of diseases. Studies have shown that Autophagy may play an important role in the process of α-amanitin-induced liver injury. However, the mechanism of α-amanitin-induced Autophagy remains unclear. Thus, this study aimed to explore the mechanisms of α-amanitin in inducing hepatotoxicity in Sprague Dawley (SD) rats and the normal human liver cell line L02 cells. The SD rats and L02 cells exposed to α-amanitin were observed to determine whether α-amanitin could induce the Autophagy of rat liver and L02 cells. The regulatory relationship between Autophagy and the AMPK-mTOR- ULK pathway by exposing the Autophagy agonist (rapamycin (RAPA)), Autophagy Inhibitor (3-methylademine (3-MA)), and AMPK Inhibitor (compound C) was also explored. Autophagy-related proteins and AMPK-mTOR-ULK pathway-related proteins were detected using Western blot. The results of the study indicated that exposure to different concentrations of α-amanitin led to morphological changes in liver cells and significantly elevated levels of ALT and AST in the serum of SD rats. Additionally, the expression levels of LC3-II, Beclin-1, ATG5, Atg7, AMPK, p-AMPK, mTOR, p-mTOR, and ULK1 were significantly increased in the rat liver. And we found that L02 cells exposed to 0.5μM α-amanitin for 6h significantly induced Autophagy and activated the AMPK-mTOR-ULK1 pathway. Pretreated with RAPA, 3-MA, and compound C for 1h, the expression levels of autophagy-related proteins and AMPK-mTOR-ULK pathway-related proteins significantly changed. Our results indicates that Autophagy and the AMPK-mTOR-ULK pathway are involved in the process of α-amanitin-induced liver injury. This study may foster the identification of actionable therapeutic targets for A. phalloides intoxication.

Keywords

AMPK-mTOR-ULK1 signaling pathway; L02 cells; autophagy; liver injury; α-amanitin.

Figures
Products