Adebayo Olufunmilayo O, Holyoak Derek T, van der Meulen Marjolein C H
Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853.
Meinig School of Biomedical Engineering, Cornell University, 113 Weill Hall, Ithaca, NY 14853.
J Biomech Eng. 2019 Jul 1;141(7):0708061-07080610. doi: 10.1115/1.4043970.
Osteoarthritis (OA) is a degenerative joint disease that affects millions of people worldwide, yet its disease mechanism is not clearly understood. Animal models have been established to study disease progression by initiating OA through modified joint mechanics or altered biological activity within the joint. However, animal models often do not have the capability to directly relate the mechanical environment to joint damage. This review focuses on a novel in vivo approach based on controlled, cyclic tibial compression to induce OA in the mouse knee. First, we discuss the development of the load-induced OA model, its different loading configurations, and other techniques used by research laboratories around the world. Next, we review the lessons learned regarding the mechanobiological mechanisms of load-induced OA and relate these findings to the current understanding of the disease. Then, we discuss the role of specific genetic and cellular pathways involved in load-induced OA progression and the contribution of altered tissue properties to the joint response to mechanical loading. Finally, we propose using this approach to test the therapeutic efficacy of novel treatment strategies for OA. Ultimately, elucidating the mechanobiological mechanisms of load-induced OA will aid in developing targeted treatments for this disabling disease.
骨关节炎(OA)是一种退行性关节疾病,影响着全球数百万人,但其发病机制尚不清楚。已经建立了动物模型,通过改变关节力学或改变关节内的生物活性来引发骨关节炎,从而研究疾病进展。然而,动物模型往往无法直接将机械环境与关节损伤联系起来。本综述重点介绍了一种基于可控的、周期性胫骨压缩在小鼠膝关节中诱导骨关节炎的新型体内方法。首先,我们讨论了负荷诱导性骨关节炎模型的发展、其不同的加载配置以及世界各地研究实验室使用的其他技术。接下来,我们回顾了关于负荷诱导性骨关节炎的力学生物学机制的经验教训,并将这些发现与目前对该疾病的理解联系起来。然后,我们讨论了特定基因和细胞途径在负荷诱导性骨关节炎进展中的作用,以及组织特性改变对关节对机械负荷反应的影响。最后,我们建议使用这种方法来测试骨关节炎新型治疗策略的治疗效果。最终,阐明负荷诱导性骨关节炎的力学生物学机制将有助于开发针对这种致残性疾病的靶向治疗方法。