Ruan Merry Z C, Dawson Brian, Jiang Ming-Ming, Gannon Francis, Heggeness Michael, Lee Brendan H L
Baylor College of Medicine, Houston, Texas 77030, USA.
Arthritis Rheum. 2013 Feb;65(2):388-96. doi: 10.1002/art.37766.
The mouse is an optimal model organism in which gene-environment interactions can be used to study the pathogenesis of osteoarthritis (OA). The gold standard for arthritis research in mice is based on histopathology and immunohistochemistry, which are labor-intensive, prone to sampling bias and technical variability, and limited in throughput. The aim of this study was to develop a new technique that assesses mouse cartilage by integrating quantitative volumetric imaging techniques.
A novel mouse model of OA was generated by cruciate ligament transection (CLT) and evaluated by histopathology and immunohistochemistry. Knee joint specimens were then imaged using a new technique that combines high-resolution micro-computed tomography (micro-CT) and phase-contrast optics followed by quantitative analyses. A comparative analysis was also performed in a previously established mouse model of OA generated by destabilization of the medial meniscus (DMM).
Phase-contrast micro-CT achieved cellular resolution of chondrocytes and quantitative assessment of parameters such as articular cartilage volume and surface area. In mouse models of OA generated by either CLT or DMM, we showed that phase-contrast micro-CT distinguished control and OA cartilage by providing quantitative measures with high reproducibility and minimal variability. Features of OA at the cellular or tissue level could also be observed in images generated by phase-contrast micro-CT.
We established an imaging technology that comprehensively assessed and quantified the 2-dimensional and 3-dimensional changes of articular cartilage. Application of this technology will facilitate the rapid and high-throughput assessment of genetic and therapeutic models of OA in mice.
小鼠是一种理想的模式生物,可利用基因-环境相互作用来研究骨关节炎(OA)的发病机制。小鼠关节炎研究的金标准基于组织病理学和免疫组织化学,这些方法劳动强度大,容易出现抽样偏差和技术变异性,且通量有限。本研究的目的是开发一种通过整合定量容积成像技术来评估小鼠软骨的新技术。
通过交叉韧带横断术(CLT)建立一种新型的OA小鼠模型,并通过组织病理学和免疫组织化学进行评估。然后使用一种结合高分辨率微型计算机断层扫描(micro-CT)和相衬光学的新技术对膝关节标本进行成像,随后进行定量分析。还对先前建立的通过内侧半月板不稳定(DMM)产生的OA小鼠模型进行了比较分析。
相衬显微CT实现了软骨细胞的细胞分辨率,并对关节软骨体积和表面积等参数进行了定量评估。在由CLT或DMM产生的OA小鼠模型中,我们表明相衬显微CT通过提供具有高重现性和最小变异性的定量测量来区分对照软骨和OA软骨。在相衬显微CT生成的图像中也可以观察到细胞或组织水平的OA特征。
我们建立了一种成像技术,可全面评估和量化关节软骨的二维和三维变化。该技术的应用将有助于对小鼠OA的遗传和治疗模型进行快速且高通量的评估。