CXC chemokines play a critical role in liver injury, recovery, and regeneration

被引:45
作者
Clarke, Callisia N. [1 ]
Kuboki, Satoshi [1 ]
Tevar, Amit [1 ]
Lentsch, Alex B. [1 ]
Edwards, Michael [1 ]
机构
[1] Univ Cincinnati, Dept Surg, Cincinnati, OH 45267 USA
关键词
Ischemia/Reperfusion; Chemokines; Inflammation; Liver regeneration; ISCHEMIA-REPERFUSION INJURY; HEPATIC ISCHEMIA/REPERFUSION INJURY; LEUKOCYTE PROTEASE INHIBITOR; INTERCELLULAR-ADHESION MOLECULE-1; NECROSIS FACTOR-ALPHA; KAPPA-B ACTIVATION; RAT HEPATOCYTES; INFLAMMATORY INJURY; UP-REGULATION; MOUSE-LIVER;
D O I
10.1016/j.amjsurg.2009.01.025
中图分类号
R61 [外科手术学];
学科分类号
摘要
BACKGROUND: Hepatic ischemia/reperfusion (I/R) injury is a principal consideration of trauma, resectional liver surgery, and transplantation. Despite improvements in supportive care, hepatic I/R injury continues to negatively impact patient outcomes because of significant tissue damage and organ dysfunction. CXC chemokines have been implicated as key mediators in the deleterious inflammatory cascade after hepatic I/R and also as important, beneficial regulators of liver recovery and regeneration. As such, their potential to mediate both beneficial and detrimental effects on hepatocytes makes them a key target for therapy. Herein, we provide a review of the inflammatory mechanisms of hepatic I/R injury, with a focus on the divergent functions of CXC chemokines in this response compared with other liver insults, and offer an explanation of this apparent paradox. DATA SOURCES: MEDLINE and PubMed. CONCLUSIONS: CXC chemokines are key mediators of both the inflammatory response to hepatic I/R as well as the recovery from this injury. Their contrasting functions in the regeneration of liver mass after an ischemic insult indicates that therapeutic manipulation of these mediator pathways should differ depending on the surgical milieu. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:415 / 419
页数:5
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