#Anti-Mouse F4/80 Antigen PE; # Anti-Human/Mouse CD11b PE-Cyanine7; #02922-60; #03221-77
J Cell Mol Med. 2023 Jul 10. doi: 10.1111/jcmm.17842.
Dandan Zhu 1, Min Huang 1, Pei Shen 2, Bei Zhang 1, Guo Chen 1, Jinling Chen 1, Lian Duan 1 3, Yinong Duan 1
Affiliations expand
- PMID: 37430471
- DOI: 10.1111/jcmm.17842
Free article
Abstract
Schistosomiasis is a tropical parasitic disease that damages the liver and poses a serious threat to human health. Macrophages play a key role in the development of liver granulomas and fibrosis by undergoing polarization from M1 to M2 type during schistosomiasis. Therefore, regulating macrophage polarization is important for controlling pathological changes that occur during this disease. Triggering receptor expressed on myeloid cells 2 (TREM2) expressed on the surface of macrophages, dendritic cells and other immune cells has been shown to play a role in inhibiting inflammatory responses and regulating M2 macrophage polarization, however its role in macrophage polarization in schistosomiasis has not been investigated. In this study, we confirmed that TREM2 expression was upregulated in the livers and peritoneal macrophages of mice infected with Schistosoma japonicum. Moreover, the TREM2 expression trend correlated with the expression of M2 macrophage polarization-related molecules in the liver tissues of S. japonicum-infected mice. Using Trem2-/- mice, we also showed that Trem2 deletion inhibited Arg1 and Ym1 expression in liver tissues. Trem2 deletion also increased the number of F4/80 + CD86+ cells in peritoneal macrophages of infected mice. In summary, our study suggests that TREM2 may be involved in M2 macrophage polarization during schistosomiasis.