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10.3727/105221617X15042750874156

http://scihub22266oqcxt.onion/10.3727/105221617X15042750874156
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C5885149!5885149!28893351
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suck abstract from ncbi


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pmid28893351      Gene+Expr 2017 ; 17 (4): 277-87
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  • Hepatic Ischemia/Reperfusion: Mechanisms of Tissue Injury, Repair, and Regeneration #MMPMID28893351
  • Konishi T; Lentsch AB
  • Gene Expr 2017[]; 17 (4): 277-87 PMID28893351show ga
  • Hepatic ischemia/reperfusion (I/R) injury is a major complication of liver surgery, including liver resection, liver transplantation, and trauma surgery. Much has been learned about the inflammatory injury response induced by I/R, including the cascade of proinflammatory mediators and recruitment of activated leukocytes. In this review, we discuss the complex network of events that culminate in liver injury after I/R, including cellular, protein, and molecular mechanisms. In addition, we address the known endogenous regulatory mediators that function to maintain homeostasis and resolve injury. Finally, we cover more recent insights into how the liver repairs and regenerates after I/R injury, a setting in which physical mass remains unchanged, but functional liver mass is greatly reduced. In this regard, we focus on recent work highlighting a novel role of CXC chemokines as important regulators of hepatocyte proliferation and liver regeneration after I/R injury.
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