Immune Netw.  2018 Jun;18(3):e24. 10.4110/in.2018.18.e24.

Dual Effect of Hepatic Macrophages on Liver Ischemia and Reperfusion Injury during Liver Transplantation

Affiliations
  • 1Department of Liver Surgery, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China. xuning123@hotmail.com
  • 2Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medicine School, Hannover 30625, Germany.
  • 3Department of Laboratory, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China.

Abstract

Ischemia-reperfusion injury (IRI) is a major complication in liver transplantation (LT) and it is closely related to the recovery of grafts' function. Researches has verified that both innate and adaptive immune system are involved in the development of IRI and Kupffer cell (KC), the resident macrophages in the liver, play a pivotal role both in triggering and sustaining the sterile inflammation. Damage-associated molecular patterns (DAMPs), released by the initial dead cell because of the ischemia insult, firstly activate the KC through pattern recognition receptors (PRRs) such as toll-like receptors. Activated KCs is the dominant players in the IRI as it can secret various pro-inflammatory cytokines to exacerbate the injury and recruit other types of immune cells from the circulation. On the other hand, KCs can also serve in a contrary way to ameliorate IRI by upregulating the anti-inflammatory factors. Moreover, new standpoint has been put forward that KCs and macrophages from the circulation may function in different way to influence the inflammation. Managements towards KCs are expected to be the effective way to improve the IRI.

Keyword

Kupffer cells; Hepatic macrophages; Ischemia-reperfusion injury; Liver transplantation; Pattern recognition receptors; Tumor necrosis factor-α

MeSH Terms

Cytokines
Hand
Immune System
Inflammation
Ischemia*
Kupffer Cells
Liver Transplantation*
Liver*
Macrophages*
Receptors, Pattern Recognition
Reperfusion Injury*
Reperfusion*
Toll-Like Receptors
Cytokines
Receptors, Pattern Recognition
Toll-Like Receptors
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