Goh Doreen, Yang Yanmeng, Lee Eng Hin, Hui James Hoi Po, Yang Zheng
Department of Orthopaedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, NUHS Tower block Level 11, Singapore 119288, Singapore.
NUS Tissue Engineering Program, Life Sciences Institute, National University of Singapore, 27 Medical Drive, DSO (Kent Ridge) Building, Level 4, Singapore 11751, Singapore.
Bioengineering (Basel). 2023 Mar 13;10(3):355. doi: 10.3390/bioengineering10030355.
Articular cartilage defects commonly result from trauma and are associated with significant morbidity. Since cartilage is an avascular, aneural, and alymphatic tissue with a poor intrinsic healing ability, the regeneration of functional hyaline cartilage remains a difficult clinical problem. Mesenchymal stem cells (MSCs) are multipotent cells with multilineage differentiation potential, including the ability to differentiate into chondrocytes. Due to their availability and ease of ex vivo expansion, clinicians are increasingly applying MSCs in the treatment of cartilage lesions. However, despite encouraging pre-clinical and clinical data, inconsistencies in MSC proliferative and chondrogenic potential depending on donor, tissue source, cell subset, culture conditions, and handling techniques remain a key barrier to widespread clinical application of MSC therapy in cartilage regeneration. In this review, we highlight the strategies to manage the heterogeneity of MSCs ex vivo for more effective cartilage repair, including reducing the MSC culture expansion period, and selecting MSCs with higher chondrogenic potential through specific genetic markers, surface markers, and biophysical attributes. The accomplishment of a less heterogeneous population of culture-expanded MSCs may improve the scalability, reproducibility, and standardisation of MSC therapy for clinical application in cartilage regeneration.
关节软骨缺损通常由创伤引起,并伴有严重的发病率。由于软骨是一种无血管、无神经和无淋巴的组织,其自身愈合能力较差,因此功能性透明软骨的再生仍然是一个棘手的临床问题。间充质干细胞(MSCs)是具有多向分化潜能的多能细胞,包括分化为软骨细胞的能力。由于其易于获取和体外扩增,临床医生越来越多地将MSCs应用于软骨损伤的治疗。然而,尽管临床前和临床数据令人鼓舞,但由于供体、组织来源、细胞亚群、培养条件和处理技术的不同,MSCs的增殖和软骨生成潜能存在差异,这仍然是MSCs疗法在软骨再生中广泛临床应用的关键障碍。在这篇综述中,我们强调了在体外管理MSCs异质性以实现更有效软骨修复的策略,包括缩短MSCs培养扩增期,以及通过特定的遗传标记、表面标记和生物物理特性选择具有更高软骨生成潜能的MSCs。实现培养扩增的MSCs群体异质性降低,可能会提高MSCs疗法在软骨再生临床应用中的可扩展性、可重复性和标准化。