Chen Yunting, Luo Chenggen, Huang Kun, Pan Xiaoli, Ao Yulei, Tian Shidan, He Mang, Li Anmao, Chen Yanjuan, Tian Mei, Chen Yong
Department of Rheumatology and Immunology, Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, China.
Department of Orthopedics, Zunyi First People's Hospital, Zunyi, 563000, China.
Inflammation. 2025 Jul 19. doi: 10.1007/s10753-025-02342-0.
Hyaluronan and proteoglycan link protein 1 (HAPLN1) secreted by fibroblast-like synoviocytes (FLSs) plays a critical role in the pathological process of inflammatory arthritis. This study aimed to investigate the impact and underlying mechanisms of HAPLN1 in an inflamed chondrocyte model. IL-1β-treated SW1353 chondrocytes were exposed to recombinant HAPLN1 (rHAPLN1). A transwell coculture system was used to assess interactions between the chondrocytes and FLSs transfected with the HAPLN1 overexpression plasmid. Cell viability and proliferation were evaluated using cell counting kit-8 (CCK-8) assay and 5-ethynyl-2'-deoxyuridine (EdU) assay. RNA sequencing and bioinformatic analyses, including the identification of differentially expressed genes (DEGs), gene functional enrichment and protein-protein interaction analyses were conducted to explore the potential mechanisms. Our fundings revealed that HAPLN also increased the levels of inflammatory mediators (TNF-α, IL-6, MMP1, MMP3, MMP9, and ADAMTS-5) in the inflamed chondrocytes, suggesting its pro-inflammatory effect. However, HAPLN1 enhanced cell viability, and the expression of Collagen II and TGF-β, the restoration effect of extracellular matrix (ECM). Bioinformatics analysis suggested the upregulated DEGs were enriched in the inflammatory processes, and the pathways related to ECM, TNF and IL-6 were activated in inflamed chondrocytes following rHAPLN1 exposure. Additionally, the protein-protein interaction networks indicated that HAPLN1 interacts with the molecules related to ECM, inflammation, and PI3K/AKT/mTOR pathway. Western blot assay further verified that the phosphorylation of PI3K, AKT, and mTOR was elevated in the rHAPLN1-treated chondrocytes. Our findings highlight the dual effects of HAPLN1 on the arthritic chondrocytes, which may be associated with the activation of the PI3K/AKT/mTOR pathway.
成纤维样滑膜细胞(FLS)分泌的透明质酸和蛋白聚糖连接蛋白1(HAPLN1)在炎症性关节炎的病理过程中起关键作用。本研究旨在探讨HAPLN1在炎症性软骨细胞模型中的影响及潜在机制。将白细胞介素-1β处理的SW1353软骨细胞暴露于重组HAPLN1(rHAPLN1)。采用Transwell共培养系统评估软骨细胞与转染HAPLN1过表达质粒的FLS之间的相互作用。使用细胞计数试剂盒-8(CCK-8)测定法和5-乙炔基-2'-脱氧尿苷(EdU)测定法评估细胞活力和增殖。进行RNA测序和生物信息学分析,包括差异表达基因(DEG)的鉴定、基因功能富集和蛋白质-蛋白质相互作用分析,以探索潜在机制。我们的研究结果显示,HAPLN还增加了炎症性软骨细胞中炎症介质(肿瘤坏死因子-α、白细胞介素-6、基质金属蛋白酶1、基质金属蛋白酶3、基质金属蛋白酶9和含血小板凝血酶敏感蛋白基序的解聚素样金属蛋白酶5)的水平,表明其促炎作用。然而,HAPLN1增强了细胞活力以及Ⅱ型胶原蛋白和转化生长因子-β的表达,具有细胞外基质(ECM)的修复作用。生物信息学分析表明,上调的DEG在炎症过程中富集,并且在rHAPLN1暴露后的炎症性软骨细胞中,与ECM、肿瘤坏死因子和白细胞介素-6相关的通路被激活。此外,蛋白质-蛋白质相互作用网络表明,HAPLN1与与ECM、炎症和PI3K/AKT/mTOR通路相关的分子相互作用。蛋白质免疫印迹分析进一步证实,rHAPLN1处理的软骨细胞中PI3K、AKT和mTOR的磷酸化水平升高。我们的研究结果突出了HAPLN1对关节炎软骨细胞的双重作用,这可能与PI3K/AKT/mTOR通路的激活有关。