Cheng Zhongfeng, Cheng Kerun, Tang Yan, Duan Xueqiong, Fu Yangshan, Duan Hongdan, Ye Yong
Department of Emergency Medicine, Affiliated Hospital of Yunnan University, Yunnan, 650021, China.
West China Clinical Medicine, Sichuan University, Sichuan, 610044, China.
Immunol Res. 2025 Mar 19;73(1):64. doi: 10.1007/s12026-025-09619-4.
Mushroom poisoning is mainly caused by α-amanitin (α-AMA), and there is currently no effective drug to treat α-AMA poisoning. Therefore, it is particularly important to find early diagnostic markers for α-AMA injury. Hepatic injury models induced by α-AMA were established both in hepatic cells and mice. The cell viability of human normal hepatic cells after α-AMA treatment was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Liver function parameters was assessed by the Enzyme-Linked Immunosorbent Assay (ELISA). Furthermore, oxidative stress was detected by 2',7'-Dichlorofluorescin Diacetate (DCFH-DA) and Dihydroethidium (DHE) staining. Autophagy- and apoptosis-related proteins were assessed by Western blot and immunofluorescence staining. We applied Hematoxylin and Eosin (H&E), Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and Oil Red O (ORO) staining to observe the degree of cell damage and hepatocyte apoptosis. In addition, mitochondrial membrane potential was also determined by JC-1 immunofluorescence staining and flow cytometry. The results showed that α-AMA decreased cell viability in a dose-dependent manner. In addition, the levels of alanine aminotransferase (ALT), aspartate transaminase (AST) and mitochondrial reactive oxygen species (mtROS) were observed to increase in the α-AMA-treated groups, whereas antioxidants superoxide dismutase (SOD) levels were reduced. Moreover, α-AMA promoted hepatocyte mitophagy and apoptosis, which were alleviated by PRDX6 overexpression. Finally, PRDX6 and Parkin were found to accumulate in mitochondria and α-AMA activated mitophagy by silencing PRDX6. Collectively, our results demonstrated that α-AMA activates oxidative stress and mitophagy by inhibiting the expression of PRDX6, leading to hepatic injury. These findings from both in vitro and in vivo models provide insights into the toxicological mechanisms of α-AMA, underscoring the potential of PRDX6 as a therapeutic target for treating α-AMA-induced hepatotoxicity. HIGHLIGHTS: α-AMA leads to ROS accumulation and activates oxidative stress. α-AMA promotes hepatocyte mitophagy and apoptosis. PRDX6 alleviates α-AMA-induced hepatic injury. PRDX6 mediates mitophagy through Parkin.
蘑菇中毒主要由α-鹅膏毒肽(α-AMA)引起,目前尚无治疗α-AMA中毒的有效药物。因此,寻找α-AMA损伤的早期诊断标志物尤为重要。在肝细胞和小鼠中均建立了由α-AMA诱导的肝损伤模型。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法评估α-AMA处理后人正常肝细胞的细胞活力。通过酶联免疫吸附测定(ELISA)评估肝功能参数。此外,用2',7'-二氯荧光素二乙酸酯(DCFH-DA)和二氢乙锭(DHE)染色检测氧化应激。通过蛋白质免疫印迹法和免疫荧光染色评估自噬和凋亡相关蛋白。我们应用苏木精和伊红(H&E)染色、末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)法和油红O(ORO)染色观察细胞损伤程度和肝细胞凋亡情况。此外,还通过JC-1免疫荧光染色和流式细胞术测定线粒体膜电位。结果表明,α-AMA以剂量依赖性方式降低细胞活力。此外,在α-AMA处理组中观察到丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)和线粒体活性氧(mtROS)水平升高,而抗氧化剂超氧化物歧化酶(SOD)水平降低。此外,α-AMA促进肝细胞线粒体自噬和凋亡,而过表达PRDX6可减轻这些现象。最后,发现PRDX6和帕金蛋白在线粒体中积累,并且通过沉默PRDX6,α-AMA激活了线粒体自噬。总的来说,我们的结果表明,α-AMA通过抑制PRDX6的表达激活氧化应激和线粒体自噬,导致肝损伤。这些来自体外和体内模型的研究结果为α-AMA的毒理学机制提供了见解,强调了PRDX6作为治疗α-AMA诱导的肝毒性治疗靶点的潜力。要点:α-AMA导致活性氧积累并激活氧化应激。α-AMA促进肝细胞线粒体自噬和凋亡。PRDX6减轻α-AMA诱导的肝损伤。PRDX6通过帕金蛋白介导线粒体自噬。