Lakin Benjamin A, Patel Harsh, Holland Conor, Freedman Jonathan D, Shelofsky Joshua S, Snyder Brian D, Stok Kathryn S, Grinstaff Mark W
Center for Advanced Orthopaedic Studies, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Department of Biomedical Engineering, Boston University, Boston, Massachusetts.
J Orthop Res. 2016 Jul;34(7):1130-8. doi: 10.1002/jor.23141. Epub 2016 Jan 6.
Mouse models of osteoarthritis (OA) are commonly used to study the disease's pathogenesis and efficacy of potential treatments. However, measuring the biochemical and mechanical properties of articular cartilage in these models currently requires destructive and time-consuming histology and mechanical testing. Therefore, we examined the feasibility of using contrast-enhanced CT (CECT) to rapidly and non-destructively image and assess the glycosaminoglycan (GAG) content. Using three ex vivo C57BL/6 mouse tibial plateaus, we determined the time required for the cationic contrast agent CA4+ to equilibrate in the cartilage. The whole-joint coefficient of friction (μ) of 10 mouse knees (some digested with Chondroitenase ABC to introduce variation in GAG) was evaluated using a modified Stanton pendulum. For both the medial and lateral tibial plateau cartilage of these knees, linear regression was used to compare the equilibrium CECT attenuations to μ, as well as each side's indentation equilibrium modulus (E) and Safranin-O determined GAG content. CA4+ equilibrated in the cartilage in 30.9 ± 0.95 min (mean ± SD, tau value of 6.17 ± 0.19 min). The mean medial and lateral CECT attenuation was correlated with μ (R(2) = 0.69, p < 0.05), and the individual medial and lateral CECT attenuations correlated with their respective GAG contents (R(2) ≥ 0.63, p < 0.05) and E (R(2) ≥ 0.63, p < 0.05). In conclusion, CECT using CA4+ is a simple, non-destructive technique for three-dimensional imaging of ex vivo mouse cartilage, and significant correlations between CECT attenuation and GAG, E, and μ are observed. © 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:1130-1138, 2016.
骨关节炎(OA)小鼠模型常用于研究该疾病的发病机制和潜在治疗方法的疗效。然而,目前在这些模型中测量关节软骨的生化和力学特性需要进行破坏性且耗时的组织学和力学测试。因此,我们研究了使用对比增强CT(CECT)快速、无损成像并评估糖胺聚糖(GAG)含量的可行性。我们使用三个离体的C57BL/6小鼠胫骨平台,确定阳离子造影剂CA4 +在软骨中达到平衡所需的时间。使用改良的斯坦顿摆评估10只小鼠膝关节(部分用软骨素酶ABC消化以引入GAG的变化)的全关节摩擦系数(μ)。对于这些膝关节的内侧和外侧胫骨平台软骨,使用线性回归比较平衡CECT衰减与μ,以及每侧的压痕平衡模量(E)和番红O测定的GAG含量。CA4 +在30.9±0.95分钟(平均值±标准差,时间常数为6.17±0.19分钟)内在软骨中达到平衡。内侧和外侧CECT平均衰减与μ相关(R(2) = 0.69,p < 0.05),内侧和外侧CECT各自的衰减与它们各自的GAG含量(R(2)≥0.63,p < 0.05)和E(R(2)≥0.63,p < 0.05)相关。总之,使用CA4 +的CECT是一种用于离体小鼠软骨三维成像的简单、无损技术,并且观察到CECT衰减与GAG、E和μ之间存在显著相关性。©2015骨科研究协会。由威利期刊公司出版。《矫形外科研究杂志》34:1130 - 1138,2016年。