Ogura Kohei, Terasaki Yasuhiro, Miyoshi-Akiyama Tohru, Terasaki Mika, Moss Joel, Noda Masatoshi, Yahiro Kinnosuke
Department of Molecular Infectiology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Pathogenic Microbe Laboratory, Research Institute, National Center for Global Health and Medicine, Tokyo, Japan.
Toxicol Sci. 2017 Apr 1;156(2):455-468. doi: 10.1093/toxsci/kfx009.
Cholix toxin (Cholix) from Vibrio cholerae is a potent virulence factor exhibiting ADP-ribosyltransferase activity on eukaryotic elongation factor 2 (eEF2) of host cells, resulting in the inhibition of protein synthesis. Administration of Cholix or its homologue Pseudomonas exotoxin A (PEA) to mice causes lethal hepatocyte damage. In this study, we demonstrate cytotoxicity of Cholix on human hepatocytes in the presence of tumor necrosis factor α (TNF-α), which has been reported to play a fatal role in PEA administered to mice. Compared with incubating HepG2 cells with Cholix alone, co-treatment with TNF-α and Cholix (TNF-α/Cholix) significantly enhanced the activation of caspases, cytochrome c release from mitochondria into cytoplasm, and poly-ADP-ribose polymerase (PARP) cleavage, while incubation with TNF-α alone or co-treatment with TNF-α/catalytically inactive Cholix did not. In the early stage of cell death, Cholix increased phosphorylation of mitogen-activated protein kinases (e.g., p38, ERK, JNK) and Akt, which was not affected by TNF-α alone. MAPK inhibitors (SP600125, SB20852, and U0126) suppressed PARP cleavage induced by TNF-α/Cholix. Protein kinase inhibitor Go6976 suppressed JNK phosphorylation and PARP cleavage by TNF-α/Cholix. In contrast, PKC activator PMA in the absence of TNF-α promoted Cholix-induced PARP cleavage. Reactive oxygen species (ROS) inhibitor, N-acetyl cysteine (NAC), suppressed TNF-α/Cholix-induced JNK and ERK phosphorylation, resulting in inhibition of PARP cleavage. These data suggest that ROS and JNK pathways are important mediators of TNF-α/Cholix-induced HepG2 cell death.
霍乱弧菌的Cholix毒素(Cholix)是一种强效毒力因子,对宿主细胞的真核延伸因子2(eEF2)具有ADP核糖基转移酶活性,导致蛋白质合成受到抑制。给小鼠注射Cholix或其同源物铜绿假单胞菌外毒素A(PEA)会导致致命的肝细胞损伤。在本研究中,我们证明了在肿瘤坏死因子α(TNF-α)存在的情况下,Cholix对人肝细胞具有细胞毒性,据报道TNF-α在给小鼠注射PEA时起致命作用。与单独用Cholix孵育HepG2细胞相比,TNF-α与Cholix共同处理(TNF-α/Cholix)显著增强了半胱天冬酶的激活、细胞色素c从线粒体释放到细胞质以及聚ADP核糖聚合酶(PARP)的裂解,而单独用TNF-α孵育或与TNF-α/无催化活性的Cholix共同处理则没有这种现象。在细胞死亡的早期阶段,Cholix增加了丝裂原活化蛋白激酶(如p38、ERK、JNK)和Akt的磷酸化,而单独的TNF-α对此没有影响。丝裂原活化蛋白激酶抑制剂(SP600125、SB20852和U0126)抑制了TNF-α/Cholix诱导的PARP裂解。蛋白激酶抑制剂Go6976抑制了TNF-α/Cholix诱导的JNK磷酸化和PARP裂解。相反,在没有TNF-α的情况下,蛋白激酶C激活剂佛波酯(PMA)促进了Cholix诱导的PARP裂解。活性氧(ROS)抑制剂N-乙酰半胱氨酸(NAC)抑制了TNF-α/Cholix诱导的JNK和ERK磷酸化,从而抑制了PARP裂解。这些数据表明,ROS和JNK信号通路是TNF-α/Cholix诱导HepG2细胞死亡的重要介质。