Mechanism of regulating macrophages/osteoclasts in attenuating wear particle-induced aseptic osteolysis

被引:11
作者
Yin, Zhaoyang [1 ]
Gong, Ge [2 ]
Liu, Xinhui [3 ]
Yin, Jian [3 ]
机构
[1] Xuzhou Med Univ, Affiliated Lianyungang Hosp, Peoples Hosp Lianyungang 1, Dept Orthoped, Lianyungang, Peoples R China
[2] Nanjing Univ, Jinling Hosp, Affiliated Hosp, Dept Geriatr,Med Sch, Nanjing, Peoples R China
[3] Nanjing Med Univ, Affiliated Jiangning Hosp, Dept Orthoped, Nanjing, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
macrophages; osteoclasts; osteolysis; wear particle; aseptic loosening; NF-KAPPA-B; MOLECULAR-WEIGHT POLYETHYLENE; RANKL-INDUCED OSTEOCLASTOGENESIS; INDUCED INFLAMMATORY OSTEOLYSIS; INDUCED BONE LOSS; CELL LUNG-CANCER; IN-VITRO; PROSTATE-CANCER; MEDIATED OSTEOCLASTOGENESIS; ANTIOXIDANT ENZYMES;
D O I
10.3389/fimmu.2023.1274679
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Joint replacement surgery is the most effective treatment for end-stage arthritis. Aseptic loosening caused by periprosthetic osteolysis is a common complication after joint replacement. Inflammation induced by wear particles derived from prosthetic biomaterials is a major cause of osteolysis. We emphasize that bone marrow-derived macrophages and their fusion-derived osteoclasts play a key role in this pathological process. Researchers have developed multiple intervention approaches to regulate macrophage/osteoclast activation. Aiming at wear particle-induced periprosthetic aseptic osteolysis, this review separately discusses the molecular mechanism of regulation of ROS formation and inflammatory response through intervention of macrophage/osteoclast RANKL-MAPKs-NF-kappa B pathway. These molecular mechanisms regulate osteoclast activation in different ways, but they are not isolated from each other. There is also a lot of crosstalk among the different mechanisms. In addition, other bone and joint diseases related to osteoclast activation are also briefly introduced. Therefore, we discuss these new findings in the context of existing work with a view to developing new strategies for wear particle-associated osteolysis based on the regulation of macrophages/osteoclasts.
引用
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页数:13
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