Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India.
Department of Science and Mathematics, Indian Institute of Information Technology Guwahati, Bongora, Guwahati, Assam, 781015, India.
Adv Healthc Mater. 2021 Oct;10(20):e2100961. doi: 10.1002/adhm.202100961. Epub 2021 Jul 24.
Osteoarthritis (OA) is a musculoskeletal disease characterized by progressive degeneration of osteochondral tissues. Current treatment is restricted to the reduction of pain and loss of function of the joint. To better comprehend the OA pathophysiological conditions, several models are employed, however; there is no consensus on a suitable model. In this review, different in vitro models being developed for possible therapeutic intervention of OA are outlined. Herein, various in vitro OA models starting from 2D model, co-culture model, 3D models, dynamic culture model to advanced technologies-based models such as 3D bioprinting, bioassembly, organoids, and organ-on-chip-based models are discussed with their advantages and disadvantages. Besides, different growth factors, cytokines, and chemicals being utilized for induction of OA condition are reviewed in detail. Furthermore, there is focus on scrutinizing different molecular and possible therapeutic targets for better understanding the mechanisms and OA therapeutics. Finally, the underlying challenges associated with in vitro models are discussed followed by future prospective. Taken together, a comprehensive overview of in vitro OA models, factors to induce OA-like conditions, and intricate molecular targets with the potential to develop personalized osteoarthritis therapeutics in the future with clinical translation is provided.
骨关节炎(OA)是一种以骨软骨组织进行性退变为特征的肌肉骨骼疾病。目前的治疗方法仅限于减轻关节疼痛和丧失功能。为了更好地了解 OA 的病理生理状况,采用了几种模型,但对于合适的模型尚无共识。在这篇综述中,概述了为 OA 的可能治疗干预而开发的不同体外模型。本文讨论了从 2D 模型、共培养模型、3D 模型、动态培养模型到基于先进技术的模型(如 3D 生物打印、生物组装、类器官和基于器官芯片的模型)等不同的体外 OA 模型,及其优缺点。此外,还详细回顾了用于诱导 OA 状态的不同生长因子、细胞因子和化学物质。此外,还重点研究了不同的分子和可能的治疗靶点,以更好地了解 OA 的机制和治疗方法。最后,讨论了与体外模型相关的潜在挑战,并对未来的发展前景进行了展望。总之,本文提供了对体外 OA 模型、诱导 OA 样条件的因素以及潜在的分子靶点的全面概述,这些靶点有可能在未来通过临床转化为 OA 患者开发个性化治疗方法。