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破骨细胞活化与炎性骨病:聚焦于破骨细胞中的受体
Authors Zhao W , Li J , Su T, Wang C, Fu Y, Li C, Hua P, Liang X, Zhu Y, Cui H
Received 18 November 2024
Accepted for publication 18 February 2025
Published 4 March 2025 Volume 2025:18 Pages 3201—3213
DOI https://doi.org/10.2147/JIR.S507269
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Adam D Bachstetter
Weijie Zhao,1,* Ji Li,1,2,* Tian Su,3,4 Chuanling Wang,5 Yonghua Fu,6 Changjia Li,1 Pengbing Hua,1 Xuelong Liang,7 Yongjun Zhu,8 Hongwang Cui1
1Key Laboratory of Emergency and Trauma of Ministry of Education, Department of Emergency Surgery, Key Laboratory of Hainan Trauma and Disaster Rescue, The First Affiliated Hospital, Hainan Medical University, Haikou, Hainan, People’s Republic of China; 2The Second Affiliated Hospital of Hainan Medical University, Haikou, Hainan, People’s Republic of China; 3Key Laboratory of Emergency and Trauma, Ministry of Education, Key Laboratory of Haikou Trauma, Key Laboratory of Hainan Trauma and Disaster Rescue, The First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, People’s Republic of China; 4Engineering Research Center for Hainan Bio-Smart Materials and Bio-Medical Devices, Key Laboratory of Hainan Functional Materials and Molecular Imaging, College of Emergency and Trauma, College of Pharmacy, Hainan Medical University, Haikou, Hainan, People’s Republic of China; 5Department of Internal Medicine of Donghu, The Second Affiliated Hospital of Hainan Medical University, Haikou, Hainan, People’s Republic of China; 6Department of Hand and Foot Microsurgery, The Second Affiliated Hospital of Hainan Medical University, Haikou, Hainan, People’s Republic of China; 7The First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong, People’s Republic of China; 8Department of Nephrology, The First Affiliated Hospital, Hainan Medical University, Haikou, Hainan, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Hongwang Cui, Key Laboratory of Emergency and Trauma of Ministry of Education, Department of Emergency Surgery, Key Laboratory of Hainan Trauma and Disaster Rescue, The First Affiliated Hospital, Hainan Medical University, Haikou, Hainan, People’s Republic of China, Email cqchw2013@sina.com Yongjun Zhu, Department of Nephrology, The First Affiliated Hospital, Hainan Medical University, Haikou, Hainan, People’s Republic of China, Email zzjjyybox@163.com
Abstract: Bone homeostasis depends on the balance between osteoblast-mediated bone formation and osteoclast-mediated bone resorption. An increasing number of studies have revealed that under inflammatory conditions, osteoclast overactivation is responsible for bone loss in relevant bone diseases. Multiple signaling pathways such as receptor activator of nuclear factor-kappa B ligand (RANKL) signaling are involved in osteoclast activation. These signaling pathways rely on various receptors expressed on the surface of osteoclast progenitor cells (OPCs) or osteoclasts, which are activated by their corresponding ligands and subsequently trigger intracellular signaling. Targeting of these receptors may exert an inhibitory effect on osteoclast activation and inflammatory bone diseases. In this review, we discuss osteoclast activation and receptors involved in this process. The role of these receptors in relevant bone diseases has also been discussed.
Keywords: osteoclast, receptor, inflammation, bone loss, osteoporosis, arthritis