López-Sánchez Laura M, Collado Juan A, Corrales Fernando J, López-Cillero Pedro, Montero José L, Fraga Enrique, Serrano Juan, De La Mata Manuel, Muntané Jordi, Rodríguez-Ariza Antonio
Liver Research Unit, Hospital Universitario Reina Sofía, Córdoba, Spain.
Free Radic Res. 2007 Jan;41(1):50-61. doi: 10.1080/10715760600943918.
Nitric oxide (NO) participates in the cell death induced by d-Galactosamine (d-GalN) in hepatocytes, and NO-derived reactive oxygen intermediates are critical contributors to protein modification and hepatocellular injury. It is anticipated that S-nitrosation of proteins will participate in the mechanisms leading to cell death in d-GalN-treated human hepatocytes. In the present study, d-GalN-induced cell death was related to augmented levels of NO production and S-nitrosothiol (SNO) content. The biotin switch assay confirmed that d-GalN increased the levels of S-nitrosated proteins in human hepatocytes. S-nitrosocysteine (CSNO) enhanced protein S-nitrosation and altered cell death parameters that were related to S-nitrosation of the executioner caspase-3. Fifteen S-nitrosated proteins participating in metabolism, antioxidative defense and cellular homeostasis were identified in human hepatocytes treated with CSNO. Among them, seven were also identified in d-GalN-treated hepatocytes. The results here reported underline the importance of the alteration of SNO homeostasis during d-GalN-induced cell death in human hepatocytes.
一氧化氮(NO)参与了d - 半乳糖胺(d - GalN)诱导的肝细胞死亡,且NO衍生的活性氧中间体是蛋白质修饰和肝细胞损伤的关键促成因素。预计蛋白质的S - 亚硝基化将参与d - GalN处理的人肝细胞中导致细胞死亡的机制。在本研究中,d - GalN诱导的细胞死亡与NO生成水平和S - 亚硝基硫醇(SNO)含量的增加有关。生物素转换法证实d - GalN增加了人肝细胞中S - 亚硝基化蛋白质的水平。S - 亚硝基半胱氨酸(CSNO)增强了蛋白质的S - 亚硝基化,并改变了与刽子手半胱天冬酶 - 3的S - 亚硝基化相关的细胞死亡参数。在用CSNO处理的人肝细胞中鉴定出了15种参与代谢、抗氧化防御和细胞稳态的S - 亚硝基化蛋白质。其中,在d - GalN处理的肝细胞中也鉴定出了7种。此处报道的结果强调了在d - GalN诱导的人肝细胞死亡过程中SNO稳态改变的重要性。