Klein Christian, Wüstefeld Torsten, Heinrich Peter C, Streetz Konrad L, Manns Michael P, Trautwein Christian
Department of Gastroenterology, Hepatology and Endocrinology, Medizinische Hochschule Hannover, Hannover, Germany.
Eur J Immunol. 2003 Aug;33(8):2251-61. doi: 10.1002/eji.200323651.
ME3738 is a new compound that attenuates liver disease in several models of acute and chronic liver inflammation. We used the concanavalin A (Con A) model to elucidate the molecular mechanisms of ME3738 to block liver cell damage. Pretreatment of BALB/c mice with ME3738 prior to Con A injection resulted in a significant reduction in liver injury. The protective effect of ME3738 prior to Con A injection was associated with a reduction in IL-6 serum levels and NF-kappaB DNA binding in liver nuclear extracts. However, STAT3 DNA binding was induced via ME3738 prior to Con A injection. Further analysis showed that ME3738 induces IL-6 serum levels and activates STAT3 DNA binding and target gene transcription. The relevance of this finding was assessed in IL-6(-/-) mice. In these animals, ME3738 induced no increase in IL-6 serum expression, and activation of IL-6-dependent pathways was not found. In addition, ME3738 did not protect IL-6(-/-) animals from Con A-induced liver failure, while IL-6 injection was still effective. Therefore, we demonstrate that ME3738 triggers IL-6 expression, which activates pathways that are relevant to protect from Con A-induced liver failure.
ME3738是一种新型化合物,在多种急性和慢性肝脏炎症模型中可减轻肝脏疾病。我们使用刀豆蛋白A(Con A)模型来阐明ME3738阻断肝细胞损伤的分子机制。在注射Con A之前用ME3738预处理BALB/c小鼠,可使肝损伤显著减轻。Con A注射前ME3738的保护作用与血清IL-6水平降低以及肝核提取物中NF-κB DNA结合减少有关。然而,在Con A注射前,ME3738可诱导STAT3 DNA结合。进一步分析表明,ME3738可诱导血清IL-6水平升高,并激活STAT3 DNA结合及靶基因转录。在IL-6基因敲除(IL-6(-/-))小鼠中评估了这一发现的相关性。在这些动物中,ME3738未诱导血清IL-6表达增加,也未发现IL-6依赖途径的激活。此外,ME3738不能保护IL-6(-/-)动物免受Con A诱导的肝衰竭,而注射IL-6仍然有效。因此,我们证明ME3738触发IL-6表达,从而激活与保护免受Con A诱导的肝衰竭相关的途径。