University of Auckland, Faculty of Engineering, 2-4 Park Ave, Grafton, Auckland, 1023, New Zealand.
University of Auckland, Faculty of Medical and Health Sciences, 85 Park Road, Grafton, 1023, Auckland, New Zealand.
J Mech Behav Biomed Mater. 2020 Dec;112:104043. doi: 10.1016/j.jmbbm.2020.104043. Epub 2020 Aug 19.
From previous investigations it has been shown that there exists healthy-appearing articular cartilage that contains collagen fibril network destructuring. It is hypothesised that such sub-micron scale destructuring not only presents an increased vulnerability to tissue scale damage following impact loading, but an increase in cell death as well. Cartilage-on-bone blocks from 12 patellae, six healthy (G0) and the other six with sub-micron fibrillar destructuring (G1), were obtained and subject to 2.3 J impact loading. Two sets of sub-samples were obtained for each block tested. One set was used to examine for the live/dead cell response using calcein-AM and propidium iodide staining, imaged with confocal microscopy. The tissue microstructural matrix was imaged from the other matched set, unstained and in its fully hydrated state, using differential interference contrast optical light microscopy. High speed imaging of the impact was used to calculate the velocity changes or coefficient of restitution (COR) and used as a proxy of energy that the tissue absorbed. A previously defined tissue matrix damage score was used to quantify the extent of fracturing and cracking in the matrix. The cell death (PCD) was counted and presented as a percentage against all cells live plus dead. The energy absorbed was 36.5% higher in G1 than in G0 (p = 0.034). However, the damage score and PCD of samples in the G1 group was much larger than the G0 group, ~300% and 161% respectively. Microscopy showed that cell death is associated to both matrix compaction and further fibrillar destructuring from the ECM to the territorial matrix regions of the chondron. Following impact loading, cartilage tissue that appears normal but contains sub-micron fibrillar matrix destructuring responds with significantly increased cell death.
从先前的研究中可以看出,存在外观健康的关节软骨,其中包含胶原纤维网络结构破坏。据推测,这种亚微米级别的结构破坏不仅会增加组织水平损伤的易感性,还会增加细胞死亡。从 12 个髌骨中获得软骨-骨块,6 个健康(G0),另外 6 个存在亚微米纤维结构破坏(G1),并对其进行 2.3 J 的冲击加载。每个测试块获得两组亚样本。一组用于使用 calcein-AM 和碘化丙啶染色检查活/死细胞反应,并用共聚焦显微镜成像。另一组来自匹配的样本,未经染色并处于完全水合状态,使用相差光镜对组织微结构基质进行成像。使用高速成像来计算冲击的速度变化或恢复系数(COR),并将其用作组织吸收的能量的代理。使用先前定义的组织基质损伤评分来量化基质中碎裂和开裂的程度。细胞死亡(PCD)被计数并表示为活细胞加死细胞的百分比。G1 组吸收的能量比 G0 组高 36.5%(p=0.034)。然而,G1 组的损伤评分和 PCD 明显大于 G0 组,分别为~300%和 161%。显微镜显示,细胞死亡与基质压缩以及 ECM 向软骨区的局域基质的进一步纤维结构破坏有关。在冲击加载后,外观正常但含有亚微米纤维基质结构破坏的软骨组织会出现明显增加的细胞死亡。