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椎间盘退变与终板异常重塑及小分子转运减少有关。

Intervertebral Disc Degeneration Is Associated With Aberrant Endplate Remodeling and Reduced Small Molecule Transport.

作者信息

Ashinsky Beth G, Bonnevie Edward D, Mandalapu Sai A, Pickup Stephen, Wang Chao, Han Lin, Mauck Robert L, Smith Harvey E, Gullbrand Sarah E

机构信息

Translational Musculoskeletal Research Center, Corporal Michael Crescenz VA Medical Center, Philadelphia, PA, USA.

McKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

J Bone Miner Res. 2020 Aug;35(8):1572-1581. doi: 10.1002/jbmr.4009. Epub 2020 Apr 2.

Abstract

The intervertebral disc is the largest avascular structure in the body, and cells within the disc rely on diffusive transport via vasculature located within the vertebral endplate to receive nutrients, eliminate waste products, and maintain disc health. However, the mechanisms by which small molecule transport into the disc occurs in vivo and how these parameters change with disc degeneration remain understudied. Here, we utilize an in vivo rabbit puncture disc degeneration model to study these interactions and provide evidence that remodeling of the endplate adjacent to the disc occurs concomitant with degeneration. Our results identify significant increases in endplate bone volume fraction, increases in microscale stiffness of the soft tissue interfaces between the disc and vertebral bone, and reductions in endplate vascularity and small molecule transport into the disc as a function of degenerative state. A neural network model identified changes in diffusion into the disc as the most significant predictor of disc degeneration. These findings support the critical role of trans-endplate transport in disease progression and will improve patient selection to direct appropriate surgical intervention and inform new therapeutic approaches to improve disc health. © 2020 American Society for Bone and Mineral Research. Published 2020. This article is a U.S. Government work and is in the public domain in the USA.

摘要

椎间盘是人体最大的无血管结构,椎间盘内的细胞依靠通过位于椎体终板内的脉管系统进行扩散运输来获取营养、清除代谢废物并维持椎间盘健康。然而,小分子在体内进入椎间盘的机制以及这些参数如何随椎间盘退变而变化仍未得到充分研究。在此,我们利用体内兔椎间盘穿刺退变模型来研究这些相互作用,并提供证据表明椎间盘相邻终板的重塑与退变同时发生。我们的结果表明,随着退变状态的变化,终板骨体积分数显著增加,椎间盘与椎骨之间软组织界面的微观硬度增加,终板血管化以及小分子向椎间盘内的运输减少。神经网络模型确定进入椎间盘的扩散变化是椎间盘退变最显著的预测指标。这些发现支持了经终板运输在疾病进展中的关键作用,并将改善患者选择以指导适当的手术干预,并为改善椎间盘健康的新治疗方法提供依据。© 2020美国骨与矿物质研究学会。2020年发表。本文是美国政府工作成果,在美国属于公共领域。

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