Small extracellular vesicles from human adipose-derived stem cells attenuate cartilage degeneration.

Extracellular vesicles human adipose-derived stem cells immune regulation osteoarthritis

Journal

Journal of extracellular vesicles
ISSN: 2001-3078
Titre abrégé: J Extracell Vesicles
Pays: United States
ID NLM: 101610479

Informations de publication

Date de publication:
2020
Historique:
received: 04 06 2019
revised: 08 01 2020
accepted: 07 02 2020
entrez: 15 4 2020
pubmed: 15 4 2020
medline: 15 4 2020
Statut: epublish

Résumé

Osteoarthritis (OA) is a chronic degenerative disease of articular cartilage that is the most common joint disease worldwide. Mesenchymal stem cells (MSCs) have been the most extensively explored for the treatment of OA. Recently, it has been demonstrated that MSC-derived extracellular vesicles (EVs) may contribute to the potential mechanisms of MSC-based therapies. In this study, we investigated the therapeutic potential of human adipose-derived stem cells EVs (hASC-EVs) in alleviating OA, along with the mechanism. EVs were isolated from the culture supernatants of hASCs by a multi-filtration system based on the tangential flow filtration (TFF) system. The isolated EVs were characterised using dynamic light scattering (DLS), transmission electron microscopy (TEM), nanoparticle tracking analysis (NTA) and flow cytometry analysis. The hASC-EVs not only promoted the proliferation and migration of human OA chondrocytes, but also maintained the chondrocyte matrix by increasing type Ⅱ collagen synthesis and decreasing MMP-1, MMP-3, MMP-13 and ADAMTS-5 expression in the presence of IL-1β

Identifiants

pubmed: 32284824
doi: 10.1080/20013078.2020.1735249
pii: 1735249
pmc: PMC7144299
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1735249

Informations de copyright

© 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of The International Society for Extracellular Vesicles.

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Auteurs

Chang Hee Woo (CH)

Department of Chemical Engineering, Hanyang University, Ansan, Korea.
Research Institute, Exostemtech Inc, Ansan, Korea.

Hark Kyun Kim (HK)

School of Pharmacy, Sungkyunkwan University, Suwon, Korea.

Gun Young Jung (GY)

School of Pharmacy, Sungkyunkwan University, Suwon, Korea.

Youn Jae Jung (YJ)

Department of Chemical Engineering, Hanyang University, Ansan, Korea.
Research Institute, Exostemtech Inc, Ansan, Korea.

Kyoung Soo Lee (KS)

Department of Chemical Engineering, Hanyang University, Ansan, Korea.

Ye Eun Yun (YE)

Department of Chemical Engineering, Hanyang University, Ansan, Korea.

Jihoon Han (J)

School of Pharmacy, Sungkyunkwan University, Suwon, Korea.

Jeongmi Lee (J)

School of Pharmacy, Sungkyunkwan University, Suwon, Korea.

Woo Sung Kim (WS)

Department of Chemical Engineering, Hanyang University, Ansan, Korea.

Ji Suk Choi (JS)

Research Institute, Exostemtech Inc, Ansan, Korea.

Siyoung Yang (S)

Department of pharmacology, Ajou University School of Medicine, Suwon, Korea.

Jae Hyung Park (JH)

Research Institute, Exostemtech Inc, Ansan, Korea.
School of Chemical Engineering, Sungkyunkwan University, Suwon, Korea.
Samsung Advanced Institute for Health Science and Technology, Sungkyunkwan University, Suwon, Korea.
Biomedical Institute for Convergence, Sungkyunkwan University, Suwon, Korea.

Dong-Gyu Jo (DG)

Research Institute, Exostemtech Inc, Ansan, Korea.
School of Pharmacy, Sungkyunkwan University, Suwon, Korea.
Samsung Advanced Institute for Health Science and Technology, Sungkyunkwan University, Suwon, Korea.
Biomedical Institute for Convergence, Sungkyunkwan University, Suwon, Korea.

Yong Woo Cho (YW)

Department of Chemical Engineering, Hanyang University, Ansan, Korea.
Research Institute, Exostemtech Inc, Ansan, Korea.

Classifications MeSH