Cartilage tissue engineering by co-transplantation of chondrocyte extracellular vesicles and mesenchymal stem cells, entrapped in chitosan-hyaluronic acid hydrogel

被引:25
作者
Heirani-Tabasi, Asieh [1 ]
Hosseinzadeh, Simzar [4 ]
Rabbani, Shahram [2 ]
Tafti, Seyed Hossein Ahmadi [2 ]
Jamshidi, Khodamorad [3 ]
Soufizomorrod, Mina [1 ]
Soleimani, Masoud [1 ,4 ]
机构
[1] Tarbiat Modares Univ, Fac Med Sci, Dept Cell Therapy & Hematol, Tehran, Iran
[2] Univ Tehran Med Sci, Res Ctr Adv Technol Cardiovasc Med, Res Inst, Cardiovasc Dis, Tehran, Iran
[3] Iran Univ Med Sci, Shafa Orthoped Hosp, Bone & Joint Reconstruct Res Ctr, Tehran, Iran
[4] Shahid Beheshti Univ Med Sci, Sch Adv Technol Med, Dept Tissue Engn & Appl Cell Sci, Tehran, Iran
关键词
mesenchymal stem cells; extracellular vesicles; human articular chondrocytes; chitosan-hyaluronic acid hydrogel; chondrogenic differentiation; ARTICULAR-CARTILAGE; SCAFFOLDS; REPAIR; DIFFERENTIATION; PROLIFERATION; EXOSOMES; DEFECTS; DEGRADATION; EXPRESSION; CULTURE;
D O I
10.1088/1748-605X/ac0cbf
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Mesenchymal stem cells (MSCs) on injectable hydrogels are mostly used to regenerate articular cartilage, which would have a variety of outcomes. Chondrocyte extracellular vesicles (EVs) have attracted many attentions for their chondrogenic differentiation capacity; however, the roles of EVs in both chondrogenic differentiation of MSCs and cartilage regeneration are poorly understood yet. In the current study, to investigate the differentiation effects of human articular chondrocyte EVs on adipose-derived MSCs, they were cultured in injectable chitosan-hyaluronic acid (CS-HA) hydrogel and then treated with chondrocyte EVs for 21 days. The continuous treatment of EVs performed on MSCs increased chondrogenic genes' expressions of SOX9 and COL2A1 and induced expression of Col II protein. In addition, glycosaminoglycans secretion was detected in the EV-treated MSCs after about 14 days. The therapeutic efficiency of this hydrogel and EVs was studied in a rabbit osteochondral defect model. MRI results revealed that the cartilage regeneration capacity of EV-treated MSCs with CS-HA hydrogel was greater than the untreated MSCs or the EV-treated MSCs without hydrogel. Moreover, histological results showed hyaline-like cartilage in the CS-HA/MSC and CS-HA/EV/MSC groups in the cartilage defect sites. These findings suggested that the chondrocyte-EVs and CS-HA hydrogel could provide the preferable niche for chondrogenic differentiation of MSCs and cartilage regeneration in osteoarthritis cartilage injuries.
引用
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页数:19
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