4.8 Article

The tissue origin effect of extracellular vesicles on cartilage and bone regeneration

期刊

ACTA BIOMATERIALIA
卷 125, 期 -, 页码 253-266

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2021.02.039

关键词

Extracellular vesicles; Exosomes; Mesenchymal stem cells; Chondrogenic differentiation; Osteogenic differentiation; Cartilage and bone regeneration

资金

  1. National Natural Science Foundation of China [81972101, 81672212]
  2. Beijing Municipal Science and Technology Commission [Z171100001017085]
  3. Beijing Municipal Natural Science Foundation [7171014, 7182175]

向作者/读者索取更多资源

Extracelluar vesicles (EVs) of mesenchymal stem cells (MSCs) from different tissue origins have varying effects on chondrogenesis and osteogenesis, with EVs from adipose-derived MSCs showing the highest efficiency. Proteomics analysis revealed potential mechanisms underlying this difference.
Extracelluar vesicles (EVs) of mesenchymal stem cells (MSCs) have been considered as a promising approach in cartilage and bone tissue engineering. In this study, for the first time, we investigated the tissue origin effect of EVs on chondrogenesis and osteogenesis of MSCs in vitro and in vivo. The results demonstrated that EVs of adipose-derived MSCs showed the most efficiency. Meanwhile, protein proteomics revealed the potential mechanisms. We provide a novel evidence that the adipose is a superior reservoir in EV-based nanotechnologies and biomaterials for cartilage and bone regeneration. Direct implantation of mesenchymal stem cells (MSCs) for cartilage and bone tissue engineering faces challenges, such as immune rejection and loss of cellular viability or functionality. As nanoscale natural particles, exosomes or small extracellular vesicles (EVs) of MSCs have potential to circumvent these problems. It is significant to investigate the impact of the tissue origin of MSCs on the therapeutic bioactivity of their corresponding EVs for cartilage and bone regeneration. Here, rat MSCs isolated from the adipose, bone marrow, and synovium are cultured to obtain their corresponding EVs (ADSC-EVs, BMSCEVs, and SMSC-EVs, respectively). The ADSC-EVs stimulate the migration, proliferation, and chondrogenic and osteogenic differentiation of BMSCs in vitro as well as cartilage and bone regeneration in a mouse model more than the BMSC-EVs or SMSC-EVs. Proteomics analysis reveals that the tissue origin contributes to the distinct protein profiles among the three types of EVs, which induced cartilage and bone regenerative capacities by potential mechanisms of regulating signaling pathways including focal adhesion, ECM-receptor interaction, actin cytoskeleton, cAMP, and PI3K-Akt signaling pathways. Consequently, these findings provide insight that the adipose may be a superior candidate in EV-based nanomedicine for cartilage and bone regeneration. Statement of significance Extracelluar vesicles (EVs) of mesenchymal stem cells (MSCs) have been considered as a promising approach in cartilage and bone tissue engineering. In this study, for the first time, we investigated the tissue origin effect of EVs on chondrogenesis and osteogenesis of MSCs in vitro and in vivo. The results demonstrated that EVs of adipose-derived MSCs showed the most efficiency. Meanwhile, protein proteomics revealed the potential mechanisms. We provide a novel evidence that the adipose is a superior reservoir in EV-based nanotechnologies and biomaterials for cartilage and bone regeneration. (c) 2021 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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