In:
Disease Markers, Hindawi Limited, Vol. 35 ( 2013), p. 573-579
Abstract:
Background . Mesenchymal stem cells (MSCs), including adipose tissue-derived mesenchymal stem cells (ADSC), are multipotent and can differentiate into various cell types possessing unique immunomodulatory features. Several clinical trials have demonstrated the safety and possible efficacy of MSCs in organ transplantation. Thus, stem cell therapy is promising for tolerance induction. In this study, we assessed the reprogramming capacity of murine ADSCs and found that CD90 (Thy-1), originally discovered as a thymocyte antigen, could be a useful marker for cell therapy. Method . Murine ADSCs were isolated from B6 mice, sorted using a FACSAria cell sorter by selection of CD 90 H i or CD 90 L o , and then transduced with four standard factors (4F; Oct4, Sox2, Klf4, and c-Myc). Results . Unsorted, CD 90 H i -sorted, and CD 90 L o -sorted murine ADSCs were reprogrammed using standard 4F transduction. CD 90 H i ADSCs showed increased numbers of alkaline phosphatase-positive colonies compared with CD 90 L o ADSCs. The relative reprogramming efficiencies of unsorted, CD 90 H i -sorted, and CD 90 L o -sorted ADSCs were 100%, 116.5%, and 74.7%, respectively. CD 90 H i cells were more responsive to reprogramming. Conclusion . CD 90 H i ADSCs had greater reprogramming capacity than CD 90 L o ADSCs, suggesting that ADSCs have heterogeneous subpopulations. Thus, CD 90 H i selection presents an effective strategy to isolate a highly suppressive subpopulation for stem cell-based tolerance induction therapy.
Type of Medium:
Online Resource
ISSN:
0278-0240
,
1875-8630
Language:
English
Publisher:
Hindawi Limited
Publication Date:
2013
detail.hit.zdb_id:
2033253-1
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