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关节软骨细胞来源的细胞外囊泡通过自噬激活促进人脐带间充质干细胞的软骨分化。

Articular chondrocyte-derived extracellular vesicles promote cartilage differentiation of human umbilical cord mesenchymal stem cells by activation of autophagy.

机构信息

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.

出版信息

J Nanobiotechnology. 2020 Nov 9;18(1):163. doi: 10.1186/s12951-020-00708-0.

Abstract

BACKGROUND

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.

RESULTS

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.

CONCLUSIONS

C-EVs play an essential role in fostering chondrogenic differentiation and proliferation of HUCMSCs, which may be beneficial for articular cartilage repair.

摘要

背景

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。

结果

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。

结论

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。

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