McCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Biomedical Engineering Graduate Program, University of Calgary, Calgary, AB, Canada.
BMC Musculoskelet Disord. 2020 Jul 3;21(1):432. doi: 10.1186/s12891-020-03363-6.
Osteoarthritis (OA) is a prevalent musculoskeletal disease resulting in progressive degeneration of the hyaline articular cartilage within synovial joints. Current repair treatments for OA often result in poor quality tissue that is functionally ineffective compared to the hyaline cartilage and demonstrates increased failure rates post-treatment. Complicating efforts to improve clinical outcomes, animal models used in pre-clinical research show significant heterogeneity in their regenerative and degenerative responses associated with their species, age, genetic/epigenetic traits, and context of cartilage injury or disease. These can lead to variable outcomes when testing and validating novel therapeutic approaches for OA. Furthermore, it remains unclear whether protection against OA among different model systems is driven by inhibition of cartilage degeneration, enhancement of cartilage regeneration, or any combination thereof.
Understanding the mechanistic basis underlying this context-dependent duality is essential for the rational design of targeted cartilage repair and OA therapies. Here, we discuss some of the critical variables related to the cross-species paradigm of degenerative and regenerative abilities found in pre-clinical animal models, to highlight that a gradient of regenerative competence within cartilage may exist across species and even in the greater human population, and likely influences clinical outcomes.
A more complete understanding of the endogenous regenerative potential of cartilage in a species specific context may facilitate the development of effective therapeutic approaches for cartilage injury and/or OA.
骨关节炎(OA)是一种常见的肌肉骨骼疾病,导致滑液关节内透明软骨进行性退化。目前 OA 的修复治疗方法常常导致组织质量差,与透明软骨相比功能无效,并在治疗后显示出更高的失败率。使临床结果改善的努力变得复杂的是,临床前研究中使用的动物模型在其与物种、年龄、遗传/表观遗传特征以及软骨损伤或疾病的背景相关的再生和退行性反应方面表现出显著的异质性。当测试和验证 OA 的新治疗方法时,这可能导致不同的结果。此外,不同模型系统之间是否对 OA 具有保护作用,是通过抑制软骨退化、增强软骨再生还是两者的组合来驱动,目前仍不清楚。
了解这种与背景相关的二元性的机制基础对于有针对性的软骨修复和 OA 治疗的合理设计至关重要。在这里,我们讨论了一些与临床前动物模型中退行性和再生能力的跨物种范例相关的关键变量,以强调在物种之间甚至在更大的人类群体中,可能存在软骨内再生能力的梯度,并且可能影响临床结果。
更全面地了解特定物种背景下软骨的内源性再生潜力可能有助于开发针对软骨损伤和/或 OA 的有效治疗方法。