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Cited 36 time in webofscience Cited 38 time in scopus
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Cell source-dependent in vivo immunosuppressive properties of mesenchymal stem cells derived from the bone marrow and synovial fluid of minipigsopen access

Authors
Lee, Won-JaeHah, Young-SoolOck, Sun-A.Lee, Jae-HoonJeon, Ryong-HoonPark, Ji-SungLee, Sang-IlRho, Na-YoungRho, Gyu-JinLee, Sung-Lim
Issue Date
1-May-2015
Publisher
ELSEVIER INC
Keywords
Mesenchymal stem cell; Synovial fluid; Immunomodulation; Differentiation; Rheumatoid arthritis
Citation
EXPERIMENTAL CELL RESEARCH, v.333, no.2, pp 273 - 288
Pages
16
Indexed
SCI
SCIE
SCOPUS
Journal Title
EXPERIMENTAL CELL RESEARCH
Volume
333
Number
2
Start Page
273
End Page
288
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/17248
DOI
10.1016/j.yexcr.2015.03.015
ISSN
0014-4827
1090-2422
Abstract
The in vitro differentiation and immunosuppressive capacity of mesenchymal stem cells (MSCs) derived from synovial fluid (SF-MSCs) and bone marrow extract (BM-MSCs) in an isogenic background of minipigs were comparatively analyzed in a collagen-induced arthritis (CIA) mouse model of rheumatoid arthritis (RA). The proliferation capacity and expression of pluripotent transcription factors (Oct3/4 and Sox2) were significantly (P < 0.05) higher in SF-MSCs than in BM-MSCs. The differentiation capacity of SF-MSCs into adipocytes, osteocytes and neurocytes was significantly (P < 0.05) lower than that of BM-MSCs, and the differentiation capacity of SF-MSCs into chondrocytes was significantly (P < 0.05) higher than that of BM-MSCs. Systemic injection of BM- and SF-MSCs significantly (P < 0.05) ameliorated the clinical symptoms of CIA mice, with SF-MSCs having significantly (P < 0.05) higher clinical and histopathological recovery scores than BM-MSCs. Furthermore, the immunosuppressive properties of SF-MSCs in CIA mice were associated with increased levels of the anti-inflammatory cytokine interleukin (IL)-10, and decreased levels of the pro-inflammatory cytokine IL-1 beta and osteoclast-related sRANKL. In conclusion, SF-MSCs exhibited eminent pluripotency and differentiation capacity into chondrocytes, addition to substantial in vivo immunosuppressive capacity by elevating IL-10 and reducing IL-1 beta levels in CIA mice. (C) 2015 The Authors. Published by Elsevier Inc.
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