What Makes Umbilical Cord Tissue-Derived Mesenchymal Stromal Cells Superior Immunomodulators When Compared to Bone Marrow Derived Mesenchymal Stromal Cells?
dc.contributor.author | Bárcia, R N | |
dc.contributor.author | Santos, J M | |
dc.contributor.author | Filipe, M | |
dc.contributor.author | Teixeira, M | |
dc.contributor.author | Martins, J P | |
dc.contributor.author | Almeida, J | |
dc.contributor.author | Água-Doce, A | |
dc.contributor.author | Almeida, S C P | |
dc.contributor.author | Varela, A | |
dc.contributor.author | Pohl, S | |
dc.contributor.author | Dittmar, K E J | |
dc.contributor.author | Calado, S | |
dc.contributor.author | Simões, S I | |
dc.contributor.author | Gaspar, M M | |
dc.contributor.author | Cruz, M E M | |
dc.contributor.author | Lindenmaier, W | |
dc.contributor.author | Graça, L | |
dc.contributor.author | Cruz, H | |
dc.contributor.author | Cruz, P E | |
dc.date.accessioned | 2016-07-04T13:23:51Z | |
dc.date.available | 2016-07-04T13:23:51Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | What Makes Umbilical Cord Tissue-Derived Mesenchymal Stromal Cells Superior Immunomodulators When Compared to Bone Marrow Derived Mesenchymal Stromal Cells? 2015, 2015:583984 Stem Cells Int | en |
dc.identifier.issn | 1687-966X | |
dc.identifier.pmid | 26064137 | |
dc.identifier.doi | 10.1155/2015/583984 | |
dc.identifier.uri | http://hdl.handle.net/10033/615464 | |
dc.description.abstract | MSCs derived from the umbilical cord tissue, termed UCX, were investigated for their immunomodulatory properties and compared to bone marrow-derived MSCs (BM-MSCs), the gold-standard in immunotherapy. Immunogenicity and immunosuppression were assessed by mixed lymphocyte reactions, suppression of lymphocyte proliferation and induction of regulatory T cells. Results showed that UCX were less immunogenic and showed higher immunosuppression activity than BM-MSCs. Further, UCX did not need prior activation or priming to exert their immunomodulatory effects. This was further corroborated in vivo in a model of acute inflammation. To elucidate the potency differences observed between UCX and BM-MSCs, gene expression related to immune modulation was analysed in both cell types. Several gene expression profile differences were found between UCX and BM-MSCs, namely decreased expression of HLA-DRA, HO-1, IGFBP1, 4 and 6, ILR1, IL6R and PTGES and increased expression of CD200, CD273, CD274, IL1B, IL-8, LIF and TGFB2. The latter were confirmed at the protein expression level. Overall, these results show that UCX seem to be naturally more potent immunosuppressors and less immunogenic than BM-MSCs. We propose that these differences may be due to increased levels of immunomodulatory surface proteins such as CD200, CD273, CD274 and cytokines such as IL1β, IL-8, LIF and TGFβ2. | |
dc.language.iso | en | en |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | * |
dc.title | What Makes Umbilical Cord Tissue-Derived Mesenchymal Stromal Cells Superior Immunomodulators When Compared to Bone Marrow Derived Mesenchymal Stromal Cells? | en |
dc.type | Article | en |
dc.contributor.department | Helmholtz Centre for infection research, Inhoffenstr. 7, 38124 Braunschweig, Germany. | en |
dc.identifier.journal | Stem cells international | en |
refterms.dateFOA | 2018-06-12T21:48:55Z | |
html.description.abstract | MSCs derived from the umbilical cord tissue, termed UCX, were investigated for their immunomodulatory properties and compared to bone marrow-derived MSCs (BM-MSCs), the gold-standard in immunotherapy. Immunogenicity and immunosuppression were assessed by mixed lymphocyte reactions, suppression of lymphocyte proliferation and induction of regulatory T cells. Results showed that UCX were less immunogenic and showed higher immunosuppression activity than BM-MSCs. Further, UCX did not need prior activation or priming to exert their immunomodulatory effects. This was further corroborated in vivo in a model of acute inflammation. To elucidate the potency differences observed between UCX and BM-MSCs, gene expression related to immune modulation was analysed in both cell types. Several gene expression profile differences were found between UCX and BM-MSCs, namely decreased expression of HLA-DRA, HO-1, IGFBP1, 4 and 6, ILR1, IL6R and PTGES and increased expression of CD200, CD273, CD274, IL1B, IL-8, LIF and TGFB2. The latter were confirmed at the protein expression level. Overall, these results show that UCX seem to be naturally more potent immunosuppressors and less immunogenic than BM-MSCs. We propose that these differences may be due to increased levels of immunomodulatory surface proteins such as CD200, CD273, CD274 and cytokines such as IL1β, IL-8, LIF and TGFβ2. |