Guangxi Engineering Center in Biomedical Materials for Tissue and Organ Regeneration, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Department of Plastic & Cosmetic Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
J Nanobiotechnology. 2020 Nov 9;18(1):163. doi: 10.1186/s12951-020-00708-0.
Umbilical cord mesenchymal stem cell (HUCMSC)-based therapies were previously utilised for cartilage regeneration because of the chondrogenic potential of MSCs. However, chondrogenic differentiation of HUCMSCs is limited by the administration of growth factors like TGF-β that may cause cartilage hypertrophy. It has been reported that extracellular vesicles (EVs) could modulate the phenotypic expression of stem cells. However, the role of human chondrogenic-derived EVs (C-EVs) in chondrogenic differentiation of HUCMSCs has not been reported.
We successfully isolated C-EVs from human multi-finger cartilage and found that C-EVs efficiently promoted the proliferation and chondrogenic differentiation of HUCMSCs, evidenced by highly expressed aggrecan (ACAN), COL2A, and SOX-9. Moreover, the expression of the fibrotic marker COL1A and hypertrophic marker COL10 was significantly lower than that induced by TGF-β. In vivo, C-EVs induced HUCMSCs accelerated the repair of the rabbit model of knee cartilage defect. Furthermore, C-EVs led to an increase in autophagosomes during the process of chondrogenic differentiation, indicating that C-EVs promote cartilage regeneration through the activation of autophagy.
C-EVs play an essential role in fostering chondrogenic differentiation and proliferation of HUCMSCs, which may be beneficial for articular cartilage repair.
脐带间充质干细胞(HUCMSC)为基础的治疗方法先前被用于软骨再生,因为间充质干细胞具有成软骨潜力。然而,HUCMSC 的软骨分化受到像 TGF-β 这样的生长因子的给药限制,这可能导致软骨肥大。据报道,细胞外囊泡(EVs)可以调节干细胞的表型表达。然而,人类软骨源性 EVs(C-EVs)在 HUCMSC 软骨分化中的作用尚未报道。
我们成功地从人多指软骨中分离出 C-EVs,并发现 C-EVs 有效地促进了 HUCMSC 的增殖和软骨分化,证据是高度表达的聚集蛋白聚糖(ACAN)、COL2A 和 SOX-9。此外,纤维化标志物 COL1A 和肥大标志物 COL10 的表达明显低于 TGF-β 诱导的表达。在体内,C-EVs 诱导 HUCMSC 加速了兔膝关节软骨缺损模型的修复。此外,C-EVs 在软骨分化过程中导致自噬体增加,表明 C-EVs 通过激活自噬促进软骨再生。
C-EVs 在促进 HUCMSC 的软骨分化和增殖中发挥重要作用,这可能有利于关节软骨修复。