Monocyte-derived macrophages contribute to the deterioration of immunological liver injury in mice

• Published in: International immunopharmacology 2023-11, Vol.124, p.111036-111036, Article 111036
• Main Authors: Ruiqi, Wu, Xiaoli, Fan, Leyu, Zhou, Mengyi, Shen, Qiaoyu, Deng, Yanyi, Zheng, Li, Yang
• Format: Article
• Language: English
• Subjects: Autoimmune hepatitis; Cenicriviroc; Chemokines; Monocytes
• ISSN: 1567-5769; 1878-1705
• DOI: 10.1016/j.intimp.2023.111036

[Display omitted] •There is infiltration of monocytes into the liver of Con A-induced immunological liver injury in mice.•The CCL2/CCR2 axis is activated and result in the recruitment of CCR2 monocytes in Con A-induced immunological liver injury in mice.•Cenicriviroc, a CCR2/CCR5 dual antagonist, can significantly alleviated liver injury in Con A-induced immunological liver injury in mice. Autoimmune hepatitis (AIH) is characterized by hepatocyte destruction, leading to lymphocyte and macrophage accumulation in the liver. However, the specific mechanisms of how macrophages participate in the occurrence and development of AIH are still unclear. In this study, we investigated the effect of monocyte-derived macrophages on Con A-induced immunological liver injury in mice and we hypothesized that inhibition of CCR2 with the dual CCR2/5 inhibitor, cenicriviroc (CVC), would attenuate Con A-induced hepatitis in mice by reducing the recruitment of monocytes into the liver. Murine experimental AIH was established by concanavalin A (Con A) injection intravenously. Macrophages were depleted by injection of clodronate liposomes in Con A-treated mice. Moreover, inhibition of the CCR2/5 signaling pathway in Con A mice is achieved by CVC. Liver injury and infiltration of monocyte-derived macrophages were assessed by serum transaminase levels, histopathology, immunohistochemistry, flow cytometry, RT–qPCR, ELISA, TUNEL assay and dihydroethidium staining. The number of macrophages in the mouse livers increased in the Con A-induced hepatitis mouse model, and flow cytometry showed a significant increase in the proportion of F4/80loCD11bhi monocyte-derived macrophages, while there was no significant change in the proportion of F4/80hiCD11blo Kupffer cells. After the depletion of liver macrophages by clodronate liposomes, the levels of serum ALT and AST, and the degree of liver tissue damage were alleviated in Con A-treated mice. Furthermore, Con A leaded an increase in the expression of a group of CC chemokines in mouse livers, and the elevation of CCL2 was prevented with the depletion of macrophages. Additionally, CVC reduced macrophage infiltration in the liver and ameliorated Con A-induced liver injury. Meanwhile, CVC reduced the apoptosis and oxidative damage of hepatocytes caused by Con A. Our research demonstrates that there is an increase in monocyte-derived macrophages in the livers due to the monocyte infiltration resulted from the activation of the CCL2-CCR2 axis in C