Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Department of Cell Engineering, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Cell Tissue Res. 2023 Oct;394(1):145-162. doi: 10.1007/s00441-023-03819-w. Epub 2023 Aug 1.
Extracellular vesicles (EVs) may have a key therapeutic role and offer an innovative treatment for osteoarthritis (OA). Studies have shown that ratio of MSC/chondrocyte could affect their therapeutic outcomes. Here, we investigate the chondrogenic potential and therapeutic effect of EVs derived from MSCs and chondrocytes in the naïve, chondrogenically primed, and co-culture states to treat OA. EVs are isolated from naïve MSCs (M-EV), chondrogenically primed MSCs (cpM-EV), chondrocytes (C-EV), and co-cultures of chondrocytes plus MSCs at ratios of 1:1 (C/M-EV), 2:1 (2C/M-EV), and 4:1 (4C/M-EV). We characterized the isolated EVs in terms of surface markers, morphology, size, and zeta potential, and evaluated their chondrogenic potential in vitro by qRT-PCR and histological analyses. Next, these EVs were intra-articularly injected into osteoarthritic cartilage of a rat model and assessed by radiography, gait parameters, and histological and immunohistochemical analyses. EVs obtained from chondrocytes co-cultured with MSCs resulted in improved matrix production and functional differentiation. Our research showed that close proximity between the two cell types was essential for this response, and improved chondrogenesis and matrix formation were the outcomes of this interaction in vitro. Furthermore, in the in vivo rat OA model induced by a monoiodoacetate (MIA), we observed recovery from OA by increasing ratio of the C/M-derived EV group compared to the other groups. Our findings show that the increasing chondrocyte ratio to MSC leads to high chondrogenic induction and the therapeutic effect of harvested EVs for cartilage repair.
细胞外囊泡 (EVs) 在骨关节炎 (OA) 的治疗中可能具有关键作用,并提供了一种创新的治疗方法。研究表明,MSC/软骨细胞的比例可能会影响其治疗效果。在这里,我们研究了来自未分化 MSC (M-EV)、软骨分化诱导的 MSC (cpM-EV)、软骨细胞 (C-EV) 以及软骨细胞和 MSC 以 1:1 (C/M-EV)、2:1 (2C/M-EV) 和 4:1 (4C/M-EV) 比例共培养状态下的 EV 在 OA 治疗中的软骨生成潜力和治疗效果。我们从表面标志物、形态、大小和 ζ 电位等方面对分离的 EV 进行了表征,并通过 qRT-PCR 和组织学分析评估了它们的体外软骨生成潜力。接下来,我们将这些 EV 关节内注射到 OA 大鼠模型的软骨中,并通过放射学、步态参数以及组织学和免疫组织化学分析进行评估。与 MSC 共培养的软骨细胞来源的 EV 可促进基质产生和功能分化。我们的研究表明,两种细胞类型的接近是产生这种反应的关键,并且体外这种相互作用的结果是软骨生成和基质形成的改善。此外,在由单碘乙酸 (MIA) 诱导的体内大鼠 OA 模型中,我们观察到 C/M 衍生 EV 组的 OA 恢复情况优于其他组。我们的研究结果表明,与 MSC 相比,增加软骨细胞的比例可提高软骨生成诱导和收获的 EV 对软骨修复的治疗效果。