Kupffer Cells in the Liver

被引:533
作者
Dixon, Laura J. [1 ,2 ,3 ]
Barnes, Mark [1 ,2 ,3 ]
Tang, Hui [1 ,2 ]
Pritchard, Michele T. [1 ,2 ]
Nagy, Laura E. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Case Western Reserve Univ, Liver Dis Res Ctr, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Pathobiol, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Mol Med, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Cleveland Clin, Dept Gastroenterol, Cleveland, OH 44106 USA
[5] Case Western Reserve Univ, Dept Nutr, Cleveland, OH 44106 USA
关键词
TUMOR-NECROSIS-FACTOR; TNF-ALPHA PRODUCTION; PLASMINOGEN-ACTIVATOR INHIBITOR-1; CARBON-TETRACHLORIDE EXPOSURE; INDUCED FATTY LIVER; CHRONIC ETHANOL; INSULIN-RESISTANCE; ADIPOSE-TISSUE; ANAPHYLATOXIN C5A; NONALCOHOLIC STEATOHEPATITIS;
D O I
10.1002/cphy.c120026
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Kupffer cells are a critical component of the mononuclear phagocytic system and are central to both the hepatic and systemic response to pathogens. Kupffer cells are reemerging as critical mediators of both liver injury and repair. Kupffer cells exhibit a tremendous plasticity; depending on the local metabolic and immune environment, then can express a range of polarized phenotypes, from the proinflammatory M1 phenotype to the alternative/M2 phenotype. Multiple M2 phenotypes can be distinguished, each involved in the resolution of inflammation and wound healing. Here, we have provided an update on recent research that has contributed to the developing delineation of the contribution of Kupffer cells to different types of liver injury, with an emphasis on alcoholic and nonalcoholic liver diseases. These recent advances in our understanding of Kupffer cell function and regulation will likely provide new insights into the potential for therapeutic manipulation of Kupffer cells to promote the resolution of inflammation and enhance wound healing in liver disease. (C) 2013 American Physiological Society.
引用
收藏
页码:785 / 797
页数:13
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