Recent Advances in Understanding of Pathogenesis of Alcohol-Associated Liver Disease

被引:51
|
作者
Wu, Xiaoqin [1 ]
Fan, Xiude [1 ]
Miyata, Tatsunori [1 ]
Kim, Adam [1 ]
Cajigas-Du Ross, Christina K. [1 ]
Ray, Semanti [1 ]
Huang, Emily [1 ]
Taiwo, Moyinoluwa [1 ]
Arya, Rakesh [1 ]
Wu, Jianguo [1 ,3 ]
Nagy, Laura E. [1 ,2 ,3 ]
机构
[1] Cleveland Clin, Dept Inflammat & Immun, Northern Ohio Alcohol Ctr, Cleveland, OH 44106 USA
[2] Cleveland Clin, Dept Gastroenterol & Hepatol, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Mol Med, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
alcohol-associated liver disease; ALD; programmed cell death; PCD; pattern recognition receptors; PRR; complement; gut-liver axis; HEPATIC STELLATE CELLS; SINUSOIDAL ENDOTHELIAL-CELLS; FATTY LIVER; ADIPOSE-TISSUE; PROTECTS MICE; COMPLEMENT-SYSTEM; APOPTOTIC PATHWAY; INDUCED STEATOSIS; DANGER SIGNALS; KUPFFER CELLS;
D O I
10.1146/annurev-pathmechdis-031521-030435
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Alcohol-associated liver disease (ALD) is one of the major diseases arising from chronic alcohol consumption and is one of the most common causes of liver-related morbidity and mortality. ALD includes asymptomatic liver steatosis, fibrosis, cirrhosis, and alcohol-associated hepatitis and its complications. The progression of ALD involves complex cell-cell and organ-organ interactions. We focus on the impact of alcohol on dysregulation of homeostatic mechanisms and regulation of injury and repair in the liver. In particular, we discuss recent advances in understanding the disruption of balance between programmed cell death and prosurvival pathways, such as autophagy and membrane trafficking, in the pathogenesis of ALD. We also summarize current understanding of innate immune responses, liver sinusoidal endothelial cell dysfunction and hepatic stellate cell activation, and gut-liver and adipose-liver cross talk in response to ethanol. In addition, we describe the current potential therapeutic targets and clinical trials aimed at alleviating hepatocyte injury, reducing inflammatory responses, and targeting gut microbiota, for the treatment of ALD.
引用
收藏
页码:411 / 438
页数:28
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