Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/38321

TitleAdipose tissue-derived stem cells do not elicit alloreactivity after chondrogenic and osteogenic differentiation
Author(s)Santos, T. C.
Rodrigues, D. B.
Cerqueira, M. T.
Pirraco, Rogério P.
Castro, António G.
Reis, R. L.
Marques, A. P.
KeywordsHuman Adipose tissue-derived stem cells
Immunomodulation
Murine Dendritic Cells
Murine Macrophages
Tissue Engineering-Regenerative Medicine
Xenogenic Approach
Issue dateSep-2015
PublisherMary Ann Liebert
JournalTissue Engineering. Part A
CitationSantos T. C., Rodrigues D. B., Cerqueira M. T., Pirraco R. P., Castro A. G., Reis R. L., Marques A. P. Adipose Tissue-derived Stem Cells do not Elicit Alloreactivity after Chondrogenic and Osteogenic Differentiation, Tissue Engineering Part A, Vol. 21, Issue S1, pp. S-1-S-413, doi:10.1089/ten.tea.2015.5000.abstracts, 2015
Abstract(s)Mesenchymal stem cells lack or express low levels of major histocompatibility complex (MHC) class II and other immunoactive costimulatory molecules rendering them â â immunoincompetentâ â . We have shown that human adipose tissue-derived stem cells (hASCs) implanted subcutaneously in mice did not elicit adverse immune responses 1. In this study we hypothesised that undifferentiated hASCs, and derived osteoblasts and chondrocytes, are able to evade xenogeneic immune system by failing activating murine bone marrow-derived macrophages (mBMMÃ s) and dendritic cells (DCs). Murine BMMÃ s or DCs were plated in direct contact with undifferentiated and osteo- or chondro-differentiated hASCs for 4 h, 10 h and 24 h. The cytokine profile was evaluated by qRT-PCR and the surface markers detected by flow cytometry. The direct interaction of both cell types was observed by time lapse microscopy. Results showed that mBMMÃ s and DCs did not depict an activated profile after contacting tissue culture polystyrene. This profile was maintained along the experiment in direct contact with undifferentiated, osteo- or chondro-differentiated hASCs. This was confirmed by the expression of IL-1, IL-4, IL-10 and TNF-a and ORAL ABSTRACTS S-43 surface markers (CD206 + + , CD336 + + , MHC II+ and CD86 + + ) detection. These data suggest the potential of hASCs in a xenogenic tissue engineering and regenerative medicine approach for research routine procedures, as well as for host immune system modulation in autoimmune diseases.
TypeAbstract
URIhttp://hdl.handle.net/1822/38321
ISSN1937-3341
Publisher versionhttp://online.liebertpub.com/doi/pdfplus/10.1089/ten.tea.2015.5000.abstracts
Peer-Reviewedyes
AccessOpen access
Appears in Collections:3B’s - Resumos em livros de atas de conferências - indexados no ISI Web of Science

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