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Atomic force microscopy imaging for nanoscale and microscale assessments of extracellular matrix in intervertebral disc and degeneration

机译:纳米级和微观椎间囊基质中纳米级和微尺度评估的原子力显微镜显微镜显微镜显微镜

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Degeneration of the intervertebral disc (IVD) is a condition that is often associated with debilitating back pain. There are no disease‐modifying treatments available to halt the progression of this ubiquitous disorder. This is partly due to a lack of understanding of extracellular matrix (ECM) changes that occur at the micro‐ and nanometer size scales as the disease progresses. Over the past decade, atomic force microscopy (AFM) has been utilized as a tool to investigate the impact of disease on nanoscale structure of ECM in bone, skin, tendon, and dentin. We have expanded this methodology to include the IVD and report the first quantitative analysis of ECM structure at submicron size scales in a murine model for progressive IVD degeneration. Collagen D‐spacing, a metric of nanoscale structure at the fibril level, was observed as a distribution of values with an overall average value of 62.5?±?2.5 nm. In degenerative discs, the fibril D‐spacing distribution shifted towards higher values in both the annulus fibrosus and nucleus pulposus (NP) ( P ?.05). A novel microstructural feature, collagen toroids , defined by a topographical pit enclosed by fibril‐forming matrix was observed in the NP. With degeneration, these microstructures became more numerous and the morphology was altered from circular (aspect ratio 1.0?±?0.1) to oval (aspect ratio 1.5?±?0.4), P ?.005. These analyses provide ECM structural details of the IVD at size scales that have historically been missing in studies of disc degeneration. Knowledge gained from these insights may aid the development of novel disease‐modifying therapeutics.
机译:椎间盘(IVD)的退化是通常与衰弱疼痛有关的病症。没有疾病修饰的治疗方法可以停止这种无处不在的病症的进展。这部分是由于在疾病进展情况下缺乏对微细和纳米大小尺度的细胞外基质(ECM)变化的变化。在过去的十年中,原子力显微镜(AFM)被用作研究疾病对骨,皮肤,肌腱和牙本质中ECM纳米级结构的影响。我们已经扩展了这种方法,包括IVD,并报告了逐步IVD变性的小鼠模型中亚微米尺寸的ECM结构的第一次定量分析。胶原D-间距,纳米级结构的度量在原纤维水平处被观察到作为总平均值为62.5°的值的分布为2.5nm。在退行性盘中,纤维D-间距分布在环纤维和髓核(NP)中移动朝向更高的值(P <β.05)。在NP中观察到由一种新的微观结构特征,胶原环形,由母纤维形成基质包围的地形坑限定。通过退化,这些微观结构变得越来越多,并且形态由圆形(纵横比1.0→±0.1)改变为椭圆形(纵横比1.5→±0.4),P <005。这些分析提供了IVD的ECM结构细节,历史上缺少光盘变性的研究。从这些见解中获得的知识可能有助于开发新型疾病改性治疗。

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