Department for Health Sciences, Medicine and Research, Center for Regenerative Medicine, Danube University Krems, Krems, Austria.
AC2T research GmbH, Wiener Neustadt, Austria.
Cartilage. 2021 Dec;13(1_suppl):496S-508S. doi: 10.1177/1947603521994900. Epub 2021 Feb 17.
During osteoarthritis progression, cartilage degrades in a manner that influences its biomechanical and biotribological properties, while chondrocytes reduce the synthesis of extracellular matrix components and become apoptotic. This study investigates the effects of inflammation on cartilage under biomechanical stress using biotribological tests.
Bovine osteochondral grafts from five animals were punched out from the medial condyle and treated with or without pro-inflammatory cytokines (interleukin-1β [IL-1β], tumor necrosis factor-α [TNF-α], IL-6) for 2 weeks. After incubation, biotribological tests were performed for 2 hours (alternating 10 minutes test and pause respectively at 39°C, 180 N, 1 Hz, and 2 mm stroke). Before and after testing, the cartilage surface was imaged with a 3-dimensional microscope. During testing, the coefficient of friction (COF) was measured, while gene expression analysis and investigation of metabolic activity of chondrocytes were carried out after testing. Histological sections of the tissue and wear debris from the test fluid were also analyzed.
After biotribological tests, surface cracks were found in both treated and untreated osteochondral grafts. In treated grafts, the COF increased, and the proteoglycan content in the cartilage tissue decreased, leading to structural changes. Chondrocytes from treated grafts showed increased expression of genes encoding for degradative enzymes, while cartilage-specific gene expression and metabolic activity exhibited no significant differences between treated and untreated groups. No measurable difference in the wear debris in the test fluid was found.
Treatment of osteochondral grafts with cytokines results in a significantly increased COF, while also leading to significant changes in cartilage proteoglycan content and cartilage matrix compression during biotribological tests.
在骨关节炎进展过程中,软骨以影响其生物力学和生物摩擦学特性的方式降解,同时软骨细胞减少细胞外基质成分的合成并发生凋亡。本研究通过生物摩擦学试验研究炎症对软骨在生物力学应激下的影响。
从五只动物的内侧髁骨中取出牛骨软骨移植物,并对其进行或不进行促炎细胞因子(白细胞介素 1β[IL-1β]、肿瘤坏死因子-α[TNF-α]、IL-6)处理 2 周。孵育后,对生物摩擦学进行 2 小时的测试(分别在 39°C、180N、1Hz 和 2mm 冲程下交替进行 10 分钟测试和暂停)。测试前后,使用三维显微镜对软骨表面进行成像。在测试过程中,测量摩擦系数(COF),测试后进行软骨细胞基因表达分析和代谢活性研究。还分析了组织的组织学切片和测试液中的磨损碎片。
生物摩擦学测试后,处理和未处理的骨软骨移植物的软骨表面均发现有表面裂纹。在处理的移植物中,COF 增加,软骨组织中的蛋白聚糖含量减少,导致结构发生变化。处理的移植物中的软骨细胞中编码降解酶的基因表达增加,而软骨特异性基因表达和代谢活性在处理组和未处理组之间没有显著差异。测试液中的磨损碎片没有可测量的差异。
用细胞因子处理骨软骨移植物会导致 COF 显著增加,同时在生物摩擦学测试过程中也会导致软骨蛋白聚糖含量和软骨基质压缩的显著变化。