Liu Timothy P, Ha Pin, Xiao Crystal Y, Kim Sang Yub, Jensen Andrew R, Easley Jeremiah, Yao Qingqiang, Zhang Xinli
Department of Orthopaedic Surgery, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Division of Oral and Systemic Health Sciences, School of Dentistry, University of California, Los Angeles, Los Angeles, CA, United States.
Front Cell Dev Biol. 2022 Sep 6;10:982199. doi: 10.3389/fcell.2022.982199. eCollection 2022.
There is an unmet need for novel and efficacious therapeutics for regenerating injured articular cartilage in progressive osteoarthritis (OA) and/or trauma. Mesenchymal stem cells (MSCs) are particularly promising for their chondrogenic differentiation, local healing environment modulation, and tissue- and organism-specific activity; however, despite early success, MSCs require further investigation in highly-translatable models prior to disseminated clinical usage. Large animal models, such as canine, porcine, ruminant, and equine models, are particularly valuable for studying allogenic and xenogenic human MSCs in a human-like osteochondral microenvironment, and thus play a critical role in identifying promising approaches for subsequent clinical investigation. In this mini-review, we focus on [1] considerations for MSC-harnessing studies in each large animal model, [2] source tissues and organisms of MSCs for large animal studies, and [3] tissue engineering strategies for optimizing MSC-based cartilage regeneration in large animal models, with a focus on research published within the last 5 years. We also highlight the dearth of standard assessments and protocols regarding several crucial aspects of MSC-harnessing cartilage regeneration in large animal models, and call for further research to maximize the translatability of future MSC findings.
对于进展性骨关节炎(OA)和/或创伤中受损关节软骨的再生,新型有效治疗方法仍存在未满足的需求。间充质干细胞(MSC)因其软骨生成分化、局部愈合环境调节以及组织和生物体特异性活性而特别具有前景;然而,尽管早期取得了成功,但在广泛临床应用之前,MSC需要在高度可转化的模型中进一步研究。大型动物模型,如犬、猪、反刍动物和马模型,对于在类似人类的骨软骨微环境中研究同种异体和异种人类MSC特别有价值,因此在确定后续临床研究的有前景方法中起着关键作用。在本综述中,我们重点关注:[1] 每种大型动物模型中利用MSC研究的注意事项;[2] 大型动物研究中MSC的来源组织和生物体;[3] 在大型动物模型中优化基于MSC的软骨再生的组织工程策略,重点关注过去5年内发表的研究。我们还强调了在大型动物模型中利用MSC进行软骨再生的几个关键方面缺乏标准评估和方案,并呼吁进行进一步研究,以最大限度地提高未来MSC研究结果的可转化性。