Department of Mechanical Engineering, Stanford University, Stanford, CA, USA; George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
Department of Mechanical Engineering, Stanford University, Stanford, CA, USA.
Osteoarthritis Cartilage. 2012 May;20(5):422-429. doi: 10.1016/j.joca.2012.01.004. Epub 2012 Jan 13.
To examine the relative susceptibility of cartilage and meniscus tissues to mechanical injury by applying a single, controlled overload and observing cellular, biochemical, and mechanical changes.
Cartilage and meniscus tissue explants in radial confinement were subjected to a range of injury by indenting to 40% strain at three different strain rates: 0.5%/s (slow), 5%/s (medium), or 50%/s (fast). Following injury, samples were cultured for either 1 or 9 days. Explants were assayed for cell metabolic activity, water content, and sulfated glycosaminoglycan (sGAG) content. Mechanical properties of explants were determined in torsional shear and unconfined compression. Conditioned medium was assayed for sGAG and lactate dehydrogenase (LDH) release.
Peak injury force increased with strain rate but both tissues displayed little to no macroscopic damage. Cell metabolism was lowest in medium and fast groups on day 1. Cell lysis increased with peak injury force and loading rate in both tissues. In contrast, sGAG content and release did not significantly vary with loading rate. Additionally, mechanical properties did not significantly vary with loading rate in either tissue.
By use of a custom confinement chamber, large peak forces were obtained without macroscopic destruction of the explants. At the loads achieved in this studied, cell damage was induced without detectable physical or compositional changes. These results indicate that sub-failure injury can induce biologic damage that may not be readily detected and could be an early event in osteoarthritis genesis.
通过施加单次受控过载来研究软骨和半月板组织对机械损伤的相对敏感性,并观察细胞、生化和力学变化。
采用径向约束的软骨和半月板组织标本,在三种不同应变速率(0.5%/s(慢)、5%/s(中)或 50%/s(快))下,将标本压痕至 40%应变,对其进行不同程度的损伤。损伤后,标本分别培养 1 天或 9 天。对标本进行细胞代谢活性、含水量和硫酸软骨素糖胺聚糖(sGAG)含量检测。采用扭转剪切和无约束压缩法测定标本的力学性能。对条件培养基进行 sGAG 和乳酸脱氢酶(LDH)释放检测。
峰值损伤力随应变速率增加而增加,但两种组织均未见明显宏观损伤。第 1 天,中速和快速组的细胞代谢最低。细胞溶解随峰值损伤力和加载速率在两种组织中均增加。相比之下,sGAG 含量和释放与加载速率无显著相关性。此外,两种组织的力学性能与加载速率无显著相关性。
采用定制的约束室,可以在不破坏标本宏观结构的情况下获得较大的峰值力。在本研究中所达到的负荷下,细胞损伤是在没有明显物理或成分变化的情况下诱导的。这些结果表明,亚失效损伤可能会引起生物损伤,而这种损伤可能不易被察觉,并且可能是骨关节炎发生的早期事件。