Su Jingyue, Sun Xuying, Chen Xin, Wei Kang, Luo Danni, Yang Shengwu, Zhang Chunwu, Xu Jian, Deng Zhenhan
Department of Orthopedics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, Zhejiang, China.
Geriatrics Center, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, Zhejiang, China.
Cell Mol Biol Lett. 2025 Jun 9;30(1):67. doi: 10.1186/s11658-025-00748-0.
Osteoarthritis (OA) is a chronic joint disease characterized by cartilage degeneration with unclear pathogenic mechanism. This study aims to discuss the regulatory role of cancerous inhibitor of protein phosphatase 2A (CIP2A) in OA pathogenesis and to elucidate the molecular mechanisms.
Mouse chondrocytes were induced by interleukin-1β (IL-1β) to mimic OA inflammation, and extracellular matrix (ECM) homeostasis and inflammatory factors were evaluated at mRNA and protein levels. A mouse model of OA was induced by destabilization of medial meniscus (DMM) surgery. Histopathological staining was used to assess the cartilage destruction of human and mouse. Osteophyte formation was observed using micro-computed tomography (CT). Downstream of CIP2A was screened by RNA sequencing and coimmunoprecipitation coupled with mass spectrometry in mouse chondrocytes.
CIP2A was downregulated in cartilage of patients with OA and DMM mouse models, as well as in IL-1β-induced mouse chondrocytes. However, CIP2A overexpression promoted ECM degradation and inflammatory processes and exacerbated cartilage destruction and osteophyte formation. By contrast, knockdown or pharmacological inhibition of CIP2A alleviated cartilage degeneration to a certain extent, with no improvement in osteophytes formation caused by OA. Mechanistically, CIP2A interacted with its downstream cell migration-inducing protein (CEMIP) and activated the nuclear factor kappa B (NF-κB) signaling pathway, resulting in the imbalance of cartilage anabolic and catabolic factors and the activation of inflammation in the development of OA. In addition, CIP2A was ubiquitinated in mouse chondrocytes, causing it to be degraded, which could be a negative feedback of CIP2A expression in OA.
CIP2A targets CEMIP to activate NF-κB signaling pathway, which in turn aggravates cartilage destruction and inflammation and ultimately accelerates OA development. Our results suggest the potential role of the CIP2A/CEMIP axis as a therapeutic target for OA.
骨关节炎(OA)是一种以软骨退变为特征的慢性关节疾病,其致病机制尚不清楚。本研究旨在探讨蛋白磷酸酶2A癌性抑制剂(CIP2A)在OA发病机制中的调控作用,并阐明其分子机制。
用白细胞介素-1β(IL-1β)诱导小鼠软骨细胞以模拟OA炎症,在mRNA和蛋白质水平评估细胞外基质(ECM)稳态和炎症因子。通过内侧半月板不稳定(DMM)手术诱导建立OA小鼠模型。采用组织病理学染色评估人和小鼠的软骨破坏情况。使用微型计算机断层扫描(CT)观察骨赘形成情况。通过RNA测序以及小鼠软骨细胞中的免疫共沉淀结合质谱法筛选CIP2A的下游分子。
在OA患者软骨、DMM小鼠模型以及IL-1β诱导的小鼠软骨细胞中,CIP2A表达下调。然而,CIP2A过表达促进ECM降解和炎症过程,加剧软骨破坏和骨赘形成。相比之下,敲低或药物抑制CIP2A在一定程度上减轻了软骨退变,但对OA所致的骨赘形成无改善作用。机制上,CIP与下游细胞迁移诱导蛋白(CEMIP)相互作用并激活核因子κB(NF-κB)信号通路,导致OA发展过程中软骨合成代谢和分解代谢因子失衡以及炎症激活。此外,CIP2A在小鼠软骨细胞中发生泛素化,导致其降解,这可能是OA中CIP2A表达的一种负反馈调节。
CIP2A靶向CEMIP激活NF-κB信号通路,进而加重软骨破坏和炎症,最终加速OA发展。我们的研究结果提示CIP2A/CEMIP轴作为OA治疗靶点的潜在作用。