Local transplantation of adipose-derived stem cells has a significant therapeutic effect in a mouse model of rheumatoid arthritis.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
20 02 2020
Historique:
received: 28 06 2019
accepted: 05 02 2020
entrez: 22 2 2020
pubmed: 23 2 2020
medline: 13 11 2020
Statut: epublish

Résumé

Adipose-derived stem cells (ADSCs) have anti-inflammatory and regenerative properties. The purpose of this study was to investigate the effect of locally administered ADSCs in a rheumatoid arthritis (RA) mouse model. In an in vivo experiment, single-cell ADSCs and three dimensionally-cultured ADSC spheroids were injected intra-articularly into the knees of RA model mice and histologically assessed. Marked improvement of synovial inflammation and articular cartilage regeneration was found in ADSC-treated mice. Proliferation, migration, and apoptosis assays of synovial fibroblasts incubated with single-cell and spheroid ADSCs were performed. The expression levels of total cytokine RNA in ADSC single cells, spheroids, and ADSC-treated inflammatory synovial fibroblasts were also evaluated by quantitative reverse transcription PCR. ADSCs suppressed the proliferation and migration of activated inflammatory cells and downregulated inflammatory cytokines. TSG-6 and TGFβ1 were significantly upregulated in ADSCs compared to controls and TGFβ1 was significantly upregulated in ADSC spheroids compared to single cells. The apoptosis rate of ADSC spheroids was significantly lower than that of single-cell ADSCs. These results indicated that intra-articular administration of ADSC single cells and spheroids was effective in an RA mouse model, offering a novel approach for the development of effective localized treatments for patients with RA.

Identifiants

pubmed: 32080313
doi: 10.1038/s41598-020-60041-2
pii: 10.1038/s41598-020-60041-2
pmc: PMC7033196
doi:

Substances chimiques

Cell Adhesion Molecules 0
Glucans 0
Tnfaip6 protein, mouse 0
Transforming Growth Factor beta1 0
laminaran 9008-22-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3076

Commentaires et corrections

Type : ErratumIn

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Auteurs

Hideki Ueyama (H)

Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Tadashi Okano (T)

Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan. ma1sa3ru@med.osaka-cu.ac.jp.

Kumi Orita (K)

Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Kenji Mamoto (K)

Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Masaaki Ii (M)

Nanobridge LLC, Osaka, Japan.

Satoshi Sobajima (S)

Sobajima Clinic, Osaka, Japan.

Hideki Iwaguro (H)

Sobajima Clinic, Osaka, Japan.

Hiroaki Nakamura (H)

Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

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Classifications MeSH