Institute of Biochemistry, Christian-Albrechts-University Kiel, Olshausenstrasse 40, Kiel, Germany.
Institute of Biochemistry, Christian-Albrechts-University Kiel, Olshausenstrasse 40, Kiel, Germany.
J Hepatol. 2016 Jun;64(6):1403-15. doi: 10.1016/j.jhep.2016.02.004. Epub 2016 Feb 8.
Interleukin 6 (IL-6) is a pleiotropic four-helix-bundle cytokine that exerts multiple functions in the body. In the liver, IL-6 is an important inducer of the acute phase response and infection defense. IL-6 is furthermore crucial for hepatocyte homeostasis and is a potent hepatocyte mitogen. It is not only implicated in liver regeneration, but also in metabolic function of the liver. However, persistent activation of the IL-6 signaling pathway is detrimental to the liver and might ultimately result in the development of liver tumors. On target cells IL-6 can bind to the signal transducing subunit gp130 either in complex with the membrane-bound or with the soluble IL-6 receptor to induce intracellular signaling. In this review we describe how these different pathways are involved in the physiology and pathophyiology of the liver. We furthermore discuss how IL-6 pathways can be selectively inhibited and therapeutically exploited for the treatment of liver pathologies.
白细胞介素 6(IL-6)是一种具有多种功能的四螺旋束细胞因子,在体内发挥多种作用。在肝脏中,IL-6 是急性反应和感染防御的重要诱导剂。IL-6 对肝细胞稳态至关重要,是一种有效的肝细胞有丝分裂原。它不仅参与肝再生,而且参与肝脏的代谢功能。然而,IL-6 信号通路的持续激活对肝脏有害,并可能最终导致肝肿瘤的发展。在靶细胞上,IL-6 可以与信号转导亚基 gp130 结合,形成与膜结合或可溶性 IL-6 受体的复合物,从而诱导细胞内信号转导。在这篇综述中,我们描述了这些不同的途径如何参与肝脏的生理学和病理生理学。我们还讨论了如何选择性抑制 IL-6 途径,并将其用于治疗肝脏疾病。