Lin Kevin H, Wu Qi, Leib Daniel J, Tang Simon Y
Department of Biology, Washington University in St. Louis, St. Louis, MO, United States.
Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO, United States.
J Mech Behav Biomed Mater. 2016 Oct;63:66-74. doi: 10.1016/j.jmbbm.2016.06.003. Epub 2016 Jun 8.
Disc degeneration is one of the leading factors that contribute to low back pain. Thus, the further understanding of the mechanisms contributing to degeneration of the intervertebral disc degeneration is critical for the development of therapies and strategies for treating low back pain. Rodent models are attractive for conducting mechanistic studies particularly because of the availability of genetically modified animals. However, current imaging technologies such as magnetic resonance imaging, do not have the ability to resolve spatial features at the tens- to single- micrometer scale. We propose here a contrast-enhanced microCT technique to conduct high-resolution imaging of the rodent intervertebral discs at 10µm spatial resolution. Based on the iodinated-hydrophilic contrast agent Ioversol, we are able to conduct high resolution imaging on rat and mouse intervertebral discs. Leveraging the hydrophilic characteristic of the contrast agent, we are able to discriminate the annulus fibrosus from the water-rich nucleus pulposus. Moreover, this technique allows for the quantitative measurement of disc morphologies and volumes, and we demonstrate the versatility of this technique on cultured live intervertebral discs. Coupled with our semi-automated segmentation technique, we are able to quantify the intervertebral disc volumes with a high degree of reproducibility. The contrast-enhanced microCT images were qualitatively and quantitatively indistinguishable from the traditional histological assessment of the same sample. Furthermore, stereological measures compared well between histology and microCT images. Taken together, the results reveal that rat and mouse intervertebral discs can be imaged longitudinally in vitro at high resolutions, with no adverse effects on viability and features of the intervertebral disc.
椎间盘退变是导致腰痛的主要因素之一。因此,进一步了解椎间盘退变的机制对于开发治疗腰痛的疗法和策略至关重要。啮齿动物模型因其可获得基因改造动物而对进行机制研究具有吸引力。然而,目前的成像技术,如磁共振成像,无法在数十到单微米尺度上分辨空间特征。我们在此提出一种对比增强型显微CT技术,以10微米的空间分辨率对啮齿动物椎间盘进行高分辨率成像。基于碘化亲水性造影剂碘海醇,我们能够对大鼠和小鼠的椎间盘进行高分辨率成像。利用造影剂的亲水性特征,我们能够区分纤维环和富含水分的髓核。此外,该技术还能对椎间盘形态和体积进行定量测量,并且我们在培养的活椎间盘上展示了该技术的多功能性。结合我们的半自动分割技术,我们能够高度可重复地量化椎间盘体积。对比增强型显微CT图像在定性和定量上与同一样本的传统组织学评估没有区别。此外,组织学和显微CT图像之间的体视学测量结果比较良好。综上所述,结果表明大鼠和小鼠的椎间盘可以在体外进行纵向高分辨率成像,且对椎间盘的活力和特征没有不利影响。