Adar3 promotes macrophage M2 polarization and alleviates viral myocarditis by activating the Wnt/β-catenin signaling pathway.
- Author:
Mengying ZHANG
1
;
Zhi LI
2
;
Weiya PEI
1
;
Shujun WAN
1
;
Xueqin LI
1
;
Kun LYU
1
;
Xiaolong ZHU
3
,
4
Author Information
1. Central Laboratory, Yijishan Hospital, Wannan Medical College, Wuhu 241001, China.
2. Department of Rheumatology, Yijishan Hospital, Wannan Medical College, Wuhu 241001, China.
3. Central Laboratory, Yijishan Hospital, Wannan Medical College, Wuhu 241001, China. *Corresponding author, E-mail: Zhuxlon3@
4. com.
- Publication Type:Journal Article
- MeSH:
Animals;
Adenosine Deaminase/metabolism*;
Macrophages/immunology*;
Wnt Signaling Pathway/genetics*;
Myocarditis/immunology*;
Mice;
Coxsackievirus Infections/metabolism*;
Male;
Mice, Inbred BALB C;
Enterovirus B, Human/physiology*;
beta Catenin/genetics*
- From:
Chinese Journal of Cellular and Molecular Immunology
2025;41(9):769-777
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the role and mechanism of RNA-Specific adenosine deaminase 3 (Adar3) in regulating macrophage polarization during Coxsackievirus B3(CVB3)-induced viral myocarditis (VM). Methods Bone marrow-derived macrophages (BMDM) from mice were cultured in vitro and induced into M1/M2 macrophages using interferon-gamma (IFN-γ)/lipopolysaccharide (LPS) or interleukin 4 (IL-4), respectively. The mRNA expression levels of Adar1, Adar2, and Adar3 in each group of cells were assessed by real-time quantitative PCR (qRT-PCR). Specific siRNAs targeting the Adar3 gene were designed, synthesized, and transiently transfected into M2 macrophages. The mRNA levels of M2 polarization-related marker genes-including arginase 1 (Arg1), chitinase 3-like molecule 3 (YM1/Chi3l3), and resistin-like molecule alpha (RELMα/FIZZ1)-were detected by qRT-PCR. RNA sequencing was performed to analyze the signaling pathways affected by Adar3. The expression levels of Wnt/β-catenin signaling pathway were further validated using qRT-PCR and Western blot. The adeno-associated virus overexpressing Adar3 was designed, synthesized, and injected into mice via tail vein. Three weeks later, a myocarditis mouse model was established. After an additional week, the phenotype and function of cardiac macrophages, as well as multiple indicators of VM (including echocardiography, body weight, histopathology and serology) were examined. Additionally, the protein levels of the Wnt/β-catenin signaling pathway were assessed. Results Compared to M0-type macrophages, the expression level of Adar3 was significantly increased in M2-type macrophages. After transfection of Adar3 siRNA, the mRNA levels of Arg1, YM1 and FIZZ1 in M2 macrophages were downregulated. RNA sequencing revealed 149 upregulated genes and 349 downregulated genes. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis and subsequent validation experiments indicated that Adar3 modulated the Wnt/β-catenin signaling pathway. In vivo experiments demonstrated that Adar3 overexpression alleviated the cardiac dysfunction of VM mice. The proportion of M1 macrophages in the heart decreased, while the proportion of M2 macrophages increased. At the same time, the Adar3 overexpression activated the Wnt/β-catenin signaling pathway. Conclusion Adar3 promotes macrophage polarization toward the M2 phenotype by activating the Wnt/β-catenin signaling pathway, thereby alleviating VM.
