Importance of Kupffer Cells in the Development of Acute Liver Injuries in Mice

被引:133
作者
Tsutsui, Hiroko [1 ]
Nishiguchi, Shuhei [2 ]
机构
[1] Hyogo Coll Med, Dept Microbiol, Nishinomiya, Hyogo 6638501, Japan
[2] Hyogo Coll Med, Dept Internal Med, Nishinomiya, Hyogo 6638501, Japan
关键词
Propionibacterium acnes; lipopolysaccharide (LPS); Toll-like receptor (TLR); inflammasome; interleukin-18 (IL-18); Fas; concanavalin A (Con A); acetaminophen (APAP); tissue factor; procoagulant and anticoagulant pathways; ACETAMINOPHEN-INDUCED HEPATOTOXICITY; TUMOR-NECROSIS-FACTOR; TISSUE FACTOR; IFN-GAMMA; THROMBIN GENERATION; DIFFERENTIATION FACTOR-88; IL-18; SECRETION; TNF-ALPHA; T-CELLS; IN-VIVO;
D O I
10.3390/ijms15057711
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Kupffer cells reside within the liver sinusoid and serve as gatekeepers. They produce pro- and anti-inflammatory cytokines and other biologically important molecules upon the engagement of pattern recognition receptors such as Toll-like receptors. Kupffer cell-ablated mice established by in vivo treatment with clodronate liposomes have revealed many important features of Kupffer cells. In this paper, we review the importance of Kupffer cells in murine acute liver injuries and focus on the following two models: lipopolysaccharide (LPS)-induced liver injury, which is induced by priming with Propionibacterium acnes and subsequent challenge with LPS, and hypercoagulability-mediated acute liver failure such as that in concanavalin A (Con A)-induced hepatitis. Kupffer cells are required for LPS sensitization induced by P. acnes and are a major cellular source of interleukin-18, which induces acute liver injury following LPS challenge. Kupffer cells contribute to Con A-induced acute liver failure by initiating pathogenic, intrasinusoidal thrombosis in collaboration with sinusoidal endothelial cells. The mechanisms underlying these models may shed light on human liver injuries induced by various etiologies such as viral infection and/or abnormal metabolism.
引用
收藏
页码:7711 / 7730
页数:20
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