Health Sciences Graduate Program, Universidade de Caxias do Sul, Caxias do Sul, Brazil.
Cell Therapy Laboratory, Universidade de Caxias do Sul, Caxias do Sul, Brazil.
Cartilage. 2021 Dec;13(2_suppl):1077S-1087S. doi: 10.1177/19476035211057244. Epub 2021 Nov 15.
This study aimed to evaluate the efficacy of hyaluronic acid in the viability and proliferation profile of human femoral-tibial joint cartilage affected by osteoarthritis using models of chondrocytes in a 2-dimensional (2D)- and 3-dimensional (3D)-based culture model by spheroids.
In vitro study of knee cartilage affected by osteoarthritis that required surgical treatment. Samples were cultured and exposed to hyaluronic acid (100 and 500 μM; intervention group) or vehicle solution. In monolayer or 2D culture, proliferation and cell viability were measured, and nuclear morphometry was analyzed by 4',6'-diamino-2-fenil-indol (DAPI) staining. The 3D-based culture established from the culture of articular cartilage of patients submitted to total knee arthroplasty evaluated the diameter, viability, and fusion ability of the chondrospheres created.
Samples from 3 patients resulted in viable cultures, with chondrocyte cells exhibiting a potential for cell proliferation and viability to establish a culture. Hyaluronic acid (100 and 500 μM) improved chondrocyte viability and proliferation up to 72 hours in contact when compared with the control group, and no nuclear irregularities in morphology cell characteristics were observed by DAPI. In the 3D evaluation, hyaluronic acid (500 μM) improved the cellular feedback mechanisms, increasing the survival and maintenance of the chondrospheres after 7 days of analysis, showing the intrinsic capacity of chondrospheres grouped in the attempt to rearrange and reestablish new articular tissue.
The 2D- and 3D-based culture models with hyaluronic acid improved chondrocyte viability and proliferation and demonstrated the ability of freshly formed chondrospheres to undergo fusion when placed together in the presence of hyaluronic acid.
本研究旨在通过软骨细胞的 2 维(2D)和 3 维(3D)球体培养模型,评估透明质酸对骨关节炎影响的人股胫关节软骨活力和增殖特性的疗效。
膝关节软骨的体外研究需要手术治疗。样本进行培养并暴露于透明质酸(100 和 500 μM;干预组)或载体溶液。在单层或 2D 培养中,测量增殖和细胞活力,并通过 4',6'-二脒-2-苯吲哚(DAPI)染色分析核形态计量学。从接受全膝关节置换术的患者关节软骨培养建立的 3D 培养评估了创建的软骨珠的直径、活力和融合能力。
来自 3 名患者的样本产生了可行的培养物,软骨细胞具有增殖和活力的潜力,以建立培养物。与对照组相比,透明质酸(100 和 500 μM)在接触时可提高至 72 小时的软骨细胞活力和增殖,并且 DAPI 未观察到细胞核形态特征的不规则性。在 3D 评估中,透明质酸(500 μM)改善了细胞反馈机制,在 7 天的分析后增加了软骨珠的存活和维持,显示出软骨珠在尝试重新排列和重新建立新的关节组织时的内在聚集能力。
基于 2D 和 3D 的培养模型联合透明质酸可提高软骨细胞活力和增殖,并证明了新形成的软骨珠在存在透明质酸时融合的能力。