Exosomes derived from hypoxia preconditioned mesenchymal stem cells laden in a silk hydrogel promote cartilage regeneration via the miR-205–5p/PTEN/AKT pathway

• Published in: Acta biomaterialia 2022-04, Vol.143, p.173-188
• Main Authors: Shen, Kai, Duan, Ao, Cheng, Jiangqi, Yuan, Tao, Zhou, Jinchun, Song, Huanghe, Chen, Zhefeng, Wan, Bin, Liu, Jiuxiang, Zhang, Xiao, Zhang, Yi, Xie, Rui, Liu, Feng, Fan, Weimin, Zuo, Qiang
• Format: Article
• Language: English
• Subjects: AKT protein; Bone marrow; Cartilage; Cartilage - metabolism; Cartilage regeneration; Chondrocytes; Exosomes; Exosomes - metabolism; Humans; Hydrogels; Hydrogels - metabolism; Hydrogels - pharmacology; Hypoxia; Hypoxia preconditioned bmscs; Mesenchymal stem cells; Mesenchymal Stem Cells - metabolism; MicroRNAs - pharmacology; miR-205–5p; Paracrine signalling; Preconditioning; Proto-Oncogene Proteins c-akt - metabolism; PTEN Phosphohydrolase - metabolism; PTEN Phosphohydrolase - pharmacology; PTEN protein; Regeneration; Repair; Silk; Silk - pharmacology; Silk fibroin; Silk fibroin hydrogel; Stem cells; Tissue engineering
• ISSN: 1742-7061; 1878-7568
• DOI: 10.1016/j.actbio.2022.02.026

Tissue engineering has promising prospects for cartilage regeneration. However, there remains an urgent need to harvest high quality seed cells. Bone marrow mesenchymal cells (BMSCs), and in particular their exosomes, might promote the function of articular chondrocytes (ACs) via paracrine mechanisms. Furthermore, preconditioned BMSCs could provide an enhanced therapeutic effect. BMSCs naturally exist in a relatively hypoxic environment (1%–5% O2); however, they are usually cultured under higher oxygen concentrations (21% O2). Herein, we hypothesized that hypoxia preconditioned exosomes (H-Exos) could improve the quality of ACs and be more conducive to cartilage repair. In our study, we compared the effects of exosomes derived from BMSCs preconditioned with hypoxia and normoxia (N-Exos) on ACs, demonstrating that H-Exos significantly promoted the proliferation, migration, anabolism and anti-inflammation effects of ACs. Furthermore, we confirmed that hypoxia preconditioning upregulated the expression of miR-205–5p in H-Exos, suggesting that ACs were promoted via the miR-205–5p/PTEN/AKT pathway. Finally, an injectable silk fibroin (SF) hydrogel containing ACs and H-Exos (SF/ACs/H-Exos) was utilized to repair cartilage defects and effectively promote cartilage regeneration in vivo. The application of SF/ACs/H-Exos hydrogel in cartilage regeneration therefore has promising prospects. Cartilage tissue engineering (CTE) has presented a promising prospect. However, the quality of seed cells is an important factor affecting the repair efficiency. Our study demonstrates for the first time that the exosomes derived from hypoxia preconditioned BMSCs (H-Exos) effectively promote the proliferation, migration and anabolism of chondrocytes and inhibit inflammation through miR-205–5p/PTEN/AKT pathway. Furthermore, we fabricated an injectable silk fibrion (SF) hydrogel to preserve and sustained release H-Exos. A complex composed of SF hydrogel, H-Exos and chondrocytes can effectively promote the regeneration of cartilage defects. Therefore, this study demonstrates that hypoxia pretreatment could optimize the therapeutic effects of BMSCs-derived exosomes, and the combination of exosomes and SF hydrogel could be a promising therapeutic method for cartilage regeneration. [Display omitted]