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Int J Biol Sci 2024; 20(6):1992-2007. doi:10.7150/ijbs.91519 This issue Cite

Research Paper

TREM2 promotes macrophage polarization from M1 to M2 and suppresses osteoarthritis through the NF-κB/CXCL3 axis

Chao Fang^1*, Rui Zhong^1*, Shuai Lu^1*, Gang Yu¹, Zhilin Liu¹, Chengyuan Yan¹, Jingyu Gao¹, Yang Tang¹, Yingming Wang^1✉, Qichun Zhao^1✉, Xinzhe Feng^2✉

1. Department of Orthopedics, The First Affiliated Hospital of USTC, Hefei, 230001, China.
2. Department of Joint Bone Disease Surgery, Changhai Hospital, Naval Medical University, Shanghai, 200433, China.
* These authors contributed equally to this work.

✉ Corresponding author: Xinzhe Feng, Department of Joint Bone Disease Surgery, Changhai Hospital, Naval Medical University, Shanghai, 200433, China (fengxinzheazxcedu.cn). Qichun Zhao, Department of Orthopedics, The First Affiliated Hospital of USTC, Hefei, 230001, China (qichunzhaoedu.cn). Yingming Wang, Department of Orthopedics, The First Affiliated Hospital of USTC, Hefei, 230001, China (15955178247com). More

Abstract

Objective: Osteoarthritis (OA) is the most prominent chronic arthritic disease, affecting over 3 billion people globally. Synovial macrophages, as immune cells, play an essential role in cartilage damage in OA. Therefore, regulating macrophages is crucial for controlling the pathological changes in OA. Triggering receptor expressed on myeloid cells 2 (TREM2), as expressed on immune cell surfaces, such as macrophages and dendritic cells, has suppressed inflammation and regulated M2 macrophage polarization but demonstrated an unknown role in synovial macrophage polarization in OA. This study aimed to investigate TREM2 expression downregulation in OA mice macrophages. Furthermore, the expression trend of TREM2 was associated with polarization-related molecule expression in macrophages of OA mice.

Results: We used TREM2 knockout (TREM2-KO) mice to observe that TREM2 deficiency significantly exacerbated the joint inflammation response in OA mice, thereby accelerating disease progression. Separating macrophages and chondrocytes from TREM2-KO mice and co-cultivating them significantly increased chondrocyte apoptosis and inhibited chondrocyte proliferation. Further, TREM2 deficiency also significantly enhanced phosphatidylinositol 3-kinase(PI3K)/AKT signaling pathway activation, increasing nuclear factor kappa light chain enhancer of activated B cells (NF-κB) signaling and C-X-C Motif Chemokine Ligand 3 (CXCL3) expression. Furthermore, NF-κB signaling pathway inhibition significantly suppressed arthritis inflammation in OA mice, thereby effectively alleviating TREM2 deficiency-related adverse effects on chondrocytes. Notably, knocking down CXCL3 of TREM2-KO mice macrophages significantly inhibits inflammatory response and promotes chondrocyte proliferation. Intravenous recombinant TREM2 protein (soluble TREM2, sTREM2) injection markedly promotes macrophage polarization from M1 to M2 and improves the joint tissue pathology and inflammatory response of OA.

Conclusion: Our study reveals that TREM2 promotes macrophage polarization from M1 to M2 during OA by NF-κB/CXCL3 axis regulation, thereby improving the pathological state of OA.

Keywords: Osteoarthritis, TREM2, Macrophage, NF-κB, CXCL3

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