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马骨髓间充质基质细胞来源的软骨样体外模型的机械刺激引发骨关节炎特征

Mechanical Stimulation of Equine Bone Marrow Mesenchymal Stromal Cell-Derived Cartilage-Like In Vitro Model Triggers Osteoarthritis Features.

作者信息

Contentin Romain, Jehl Cassie, Commenchail Kevin, Legendre Florence, Galéra Philippe, Cassé Frédéric, Demoor Magali

机构信息

Université Caen Normandie, Normandie Univ, BIOTARGEN UR7450, Normandie Equine Valée, GIS CENTAURE, F-14000 Caen, France.

出版信息

ACS Biomater Sci Eng. 2025 Jul 14;11(7):4153-4165. doi: 10.1021/acsbiomaterials.5c00500. Epub 2025 Jun 13.

Abstract

Osteoarthritis (OA) affects millions of people globally, causing irreversible cartilage damage, chronic inflammation, and progressive joint dysfunction. Similarly, horses can develop OA spontaneously or due to their athletic careers, influenced by mechanical and biochemical factors. Current treatments primarily focus on symptom relief without promoting cartilage regeneration. In line with the 3Rs principles (refine, reduce, replace), the development of OA models is essential for advancing new therapeutic approaches against OA. In response to this need, the present study aimed to develop an model of mechanically induced OA. Bone marrow-derived mesenchymal stromal cells (BM-MSCs) were cultured in a biomaterial scaffold and differentiated for 21 days using a chondrogenic medium to produce cartilage-like models. The cartilage-like models underwent mechanical stimulation (compression) for 3 and 7 days at pressures sufficient to induce injurious stress. BM-MSC-derived chondrocytes express the transient receptor potential vanilloid-type 4 (TRPV4) channel and are responsive to mechanical stimulation. Mechanical stimulation was found to reduce cell proliferation without inducing cell death. The overall protein levels of type II collagen drastically declined after both 3 and 7 days of mechanical stimulation. Additionally, glycosaminoglycan (GAG) content within the cartilage-like models decreased, whereas GAG release into the supernatant increased following mechanical stimulation. Ultimately, compression led to the upregulation of catabolic factors and inflammatory mediators. In conclusion, this model successfully replicates several key features of OA, making it a valuable tool for investigating the disease's mechanisms and testing new therapeutic strategies.

摘要

骨关节炎(OA)在全球影响着数百万人,会导致不可逆的软骨损伤、慢性炎症和进行性关节功能障碍。同样,马也会自发患上OA,或者由于其运动生涯,在机械和生化因素的影响下发病。目前的治疗主要集中在缓解症状,而不促进软骨再生。根据3R原则(优化、减少、替代),OA模型的开发对于推进针对OA的新治疗方法至关重要。为满足这一需求,本研究旨在建立一种机械诱导性OA模型。将骨髓间充质基质细胞(BM-MSCs)接种于生物材料支架中,并用软骨形成培养基培养21天,以生成类软骨模型。类软骨模型在足以诱导损伤性应力的压力下接受3天和7天的机械刺激(压缩)。BM-MSC来源的软骨细胞表达瞬时受体电位香草酸亚型4(TRPV4)通道,并对机械刺激有反应。发现机械刺激会减少细胞增殖但不诱导细胞死亡。在机械刺激3天和7天后,II型胶原蛋白的总体蛋白水平均大幅下降。此外,类软骨模型中的糖胺聚糖(GAG)含量降低,而机械刺激后GAG释放到上清液中的量增加。最终,压缩导致分解代谢因子和炎症介质上调。总之,该模型成功复制了OA的几个关键特征,使其成为研究该疾病机制和测试新治疗策略的宝贵工具。

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