Mechanisms of Inflammasome Activation and Involvement in Liver Disease

A. Baral
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Abstract

The liver is a multi-potent organ with important metabolic, immunological and endocrine functions. Hepatic physiology is maintained at a balanced state via the delicate actions of different liver-resident cells. Among several factors that modulate hepatic physiology, the harmony between the activity of pro- and anti-inflammatory cytokines is a crucial determinant. However, initiation of inflammatory activity can be detrimental if it goes unresolved, leading to severe consequences such as hepatitis, hepatic fibrosis, cirrhosis or even hepatocellular carcinoma (HCC). Different physiological processes can modulate the hepatic microenvironment; one such factor is a cytosolic protein complex called the inflammasome. Inflammasome activation is a consequence of the cellular encounter with pathogens or products of cellular damage. Once activated, inflammasomes promote the maturation of interleukin-1 family cytokines such as IL-1β and IL-18 via activation of caspase-1. These cytokines have a very potent role in modulating hepatic physiology. Various lines of reports suggest that inflammasome activation and IL-1 cytokines play critical roles in liver diseases, including hepatitis, hepatic fibrosis and HCC. Conversely, inhibition of inflammasome activation and/or IL-1 signaling prevents such effects. This review summarizes the mechanisms leading to inflammasome activation and the role it plays in hepatic physiology.
炎症小体激活和参与肝病的机制
肝脏是一个多功能器官,具有重要的代谢、免疫和内分泌功能。肝脏生理机能通过不同肝脏驻留细胞的微妙作用维持平衡状态。在调节肝脏生理机能的多种因素中,促炎细胞因子和抗炎细胞因子之间的协调是一个关键的决定因素。然而,如果炎症活动得不到缓解,就会导致肝炎、肝纤维化、肝硬化甚至肝细胞癌(HCC)等严重后果。不同的生理过程可以调节肝脏微环境;其中一个因素是一种称为炎性体的细胞膜蛋白复合物。炎症小体的激活是细胞遭遇病原体或细胞损伤产物的结果。一旦激活,炎性体就会通过激活 caspase-1 促进白细胞介素-1 家族细胞因子(如 IL-1β 和 IL-18)的成熟。这些细胞因子在调节肝脏生理机能方面具有非常强大的作用。各种报告表明,炎性体激活和 IL-1 细胞因子在肝炎、肝纤维化和 HCC 等肝病中发挥着关键作用。相反,抑制炎性体活化和/或 IL-1 信号传导则可防止这些影响。本综述总结了导致炎性体活化的机制及其在肝脏生理学中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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