Yan Wan-Ting, Wang Jing-Song, Guo Shu-Yang, Zhu Jia-Hao, Zhang Zheng-Zheng
Department of Sports Medicine, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, P.R. China.
Cartilage. 2024 Jul 26:19476035241266579. doi: 10.1177/19476035241266579.
Meniscus progenitor cells (MPCs) have been identified as promising candidates for meniscus regeneration, and it is crucial for us to understand meniscus injury repair mechanism at the cellular level. In this study, we investigate the biological properties of MPCs isolated from different species using the differential adhesion to fibronectin (DAF) technique. We aim to characterize MPCs in different species and evaluate the feasibility of these models for future meniscal investigation.
MPCs were isolated from freshly digested meniscus from rat, rabbit, goat, and human cells using DAF. Biological properties, including proliferation, colony-forming, multilineage differentiation, and migration abilities, were compared in MPCs and their corresponding mixed meniscus cell (MCs) population in each species.
MPCs were successfully isolated by the DAF technique in all species. Rat MPCs appeared cobblestone-like, rabbit MPCs were more polygonal, goat MPCs had a spindle-shaped morphology, human MPCs appear more fibroblast-like. Compared with MCs, isolated MPCs showed progenitor cell characteristics, including multilineage differentiation ability and MSC (mesenchymal stem cells) markers (CD166, CD90, CD44, Stro-1) expression. They also highly expressed fibronectin receptors CD49e and CD49c. MPCs also showed greater proliferation capacity and retained colony-forming ability. Except for goat MPCs showed greater migration abilities than MCs, no significant differences were found in the migration ability between MPCs and MCs in other species.
Our study shows that DAF is an effective method for isolating MPCs from rat, rabbit, goat, and human. MPCs in these species demonstrated similar characteristics, including greater proliferation ability and better chondrogenic potential.
半月板祖细胞(MPCs)已被确定为半月板再生的有前景的候选细胞,对我们而言,在细胞水平上了解半月板损伤修复机制至关重要。在本研究中,我们使用纤连蛋白差异黏附(DAF)技术研究从不同物种分离的MPCs的生物学特性。我们旨在表征不同物种中的MPCs,并评估这些模型用于未来半月板研究的可行性。
使用DAF从大鼠、兔、山羊和人类的新鲜消化半月板中分离MPCs。比较了每个物种中MPCs及其相应的混合半月板细胞(MCs)群体的生物学特性,包括增殖、集落形成、多向分化和迁移能力。
通过DAF技术在所有物种中均成功分离出MPCs。大鼠MPCs呈鹅卵石样,兔MPCs更呈多边形,山羊MPCs呈纺锤形形态,人类MPCs更呈成纤维细胞样。与MCs相比,分离出的MPCs表现出祖细胞特征,包括多向分化能力和间充质干细胞(MSC)标志物(CD166、CD90、CD44、Stro-1)表达。它们还高表达纤连蛋白受体CD49e和CD49c。MPCs还表现出更强的增殖能力并保留了集落形成能力。除山羊MPCs的迁移能力比MCs更强外,其他物种中MPCs和MCs之间的迁移能力未发现显著差异。
我们的研究表明,DAF是从大鼠、兔、山羊和人类中分离MPCs的有效方法。这些物种中的MPCs表现出相似的特征,包括更强的增殖能力和更好的软骨形成潜力。