کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2166987 1645490 2014 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Paradoxical effects of human adipose tissue-derived mesenchymal stem cells on progression of experimental arthritis in SKG mice
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Paradoxical effects of human adipose tissue-derived mesenchymal stem cells on progression of experimental arthritis in SKG mice
چکیده انگلیسی


• Therapeutic effects of mesenchymal stem cells were tested in SKG arthritis model.
• The effects were paradoxical depending on the disease phase, early or late.
• T cells from each group, after MSC treatment, differed in their cytokine secretion.
• The results suggest different actions of the cells depending on the disease phase.
• Cautions should be paid for safe and effective use of MSCs.

We evaluated the therapeutic effect of human adipose tissue-derived mesenchymal stem cells (hAd-MSCs) in a SKG arthritis model, a relevant animal model for human rheumatoid arthritis. hAd-MSCs were administered intraperitoneally into the mice for five consecutive days from on day 12 or 34 after arthritis induction, when the average clinical score was 0.5 or 5, respectively. They remarkably suppressed arthritis when administered on day 12. Disease suppression was correlated with reduction of pro-inflammatory cytokines and with increased levels of TGF-β and IL-10 from splenocytes. However, when hAd-MSCs were administered on day 34, the clinical scores were not improved, the histopathological scores were aggravated, and cytokine profiles were differed. Thus, hAd-MSCs showed paradoxical effects, according to the disease phase when they were administered. These suggest that the same cells acted differently depending on the disease progress, and cautions should be paid for safe and effective use of MSCs.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cellular Immunology - Volume 292, Issues 1–2, November–December 2014, Pages 94–101
نویسندگان
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