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与骨关节炎:功能、调节因子及治疗策略

and Osteoarthritis: Functions, Regulatory Factors, and Treatment Strategies.

作者信息

Fu Peng-Jie, Zheng Sheng-Yuan, Luo Yan, Ren Zhuo-Qun, Li Zi-Han, Wang Ya-Ping, Lu Bang-Bao

机构信息

Department of Orthopedics, Xiangya Hospital, Central South University, Changsha 410008, China.

National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha 410008, China.

出版信息

Biomedicines. 2025 Mar 12;13(3):693. doi: 10.3390/biomedicines13030693.

Abstract

Proteoglycan 4 (PRG4), also known as lubricin, plays a critical role in maintaining joint homeostasis by reducing friction between articular cartilage surfaces and preventing cartilage degradation. Its deficiency leads to early-onset osteoarthritis (OA), while overexpression can protect against cartilage degeneration. Beyond its lubricating properties, PRG4 exerts anti-inflammatory effects by interacting with Toll-like receptors, modulating inflammatory responses within the joint. The expression of is regulated by various factors, including mechanical stimuli, inflammatory cytokines, transcription factors such as Creb5 and FoxO, and signaling pathways like TGF-β, EGFR, and Wnt/β-catenin. Therapeutic strategies targeting in OA have shown promising results, including recombinant PRG4 protein injections, gene therapies, and small molecules that enhance endogenous expression or mimic its function. Further research into the molecular mechanisms regulating expression will be essential in developing more effective OA treatments. Understanding the interplay between and other signaling pathways could reveal novel therapeutic targets. Additionally, advancements in gene therapy and biomaterials designed to deliver PRG4 in a controlled manner may hold potential for the long-term management of OA, improving patient outcomes and delaying disease progression.

摘要

蛋白聚糖4(PRG4),也称为润滑素,通过减少关节软骨表面之间的摩擦并防止软骨降解,在维持关节稳态中起关键作用。其缺乏会导致早发性骨关节炎(OA),而过度表达则可防止软骨退变。除了其润滑特性外,PRG4还通过与Toll样受体相互作用发挥抗炎作用,调节关节内的炎症反应。PRG4的表达受多种因素调节,包括机械刺激、炎性细胞因子、转录因子如Creb5和FoxO,以及信号通路如TGF-β、EGFR和Wnt/β-连环蛋白。针对OA中PRG4的治疗策略已显示出有前景的结果,包括重组PRG4蛋白注射、基因疗法以及增强内源性PRG4表达或模拟其功能的小分子。进一步研究调节PRG4表达的分子机制对于开发更有效的OA治疗至关重要。了解PRG4与其他信号通路之间的相互作用可能会揭示新的治疗靶点。此外,基因疗法和旨在以可控方式递送PRG4的生物材料的进展可能对OA的长期管理具有潜力,改善患者预后并延缓疾病进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1905/11940178/ab8c66fb7f37/biomedicines-13-00693-g001.jpg

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