What Makes Umbilical Cord Tissue-Derived Mesenchymal Stromal Cells Superior Immunomodulators When Compared to Bone Marrow Derived Mesenchymal Stromal Cells?

被引:80
作者
Barcia, R. N. [1 ]
Santos, J. M. [1 ]
Filipe, M. [1 ]
Teixeira, M. [1 ]
Martins, J. P. [1 ]
Almeida, J. [1 ]
Agua-Doce, A. [2 ]
Almeida, S. C. P. [2 ]
Varela, A. [2 ]
Pohl, S. [3 ]
Dittmar, K. E. J. [3 ]
Calado, S. [4 ]
Simoes, S. I. [4 ]
Gaspar, M. M. [4 ]
Cruz, M. E. M. [4 ]
Lindenmaier, W. [3 ]
Graca, L. [2 ]
Cruz, H. [1 ]
Cruz, P. E. [1 ]
机构
[1] ECBio SA, R&D Biotechnol, P-2700451 Amadora, Portugal
[2] Univ Lisbon, Fac Med, Inst Mol Med, P-1649028 Lisbon, Portugal
[3] Helmholtz Ctr Infect Res, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany
[4] Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, P-1649003 Lisbon, Portugal
关键词
STEM-CELLS; T-LYMPHOCYTE; IMMUNE PROPERTIES; IFN-GAMMA; PROLIFERATION; DIFFERENTIATION; SUPPRESSION; EXPRESSION; INDUCE; MECHANISMS;
D O I
10.1155/2015/583984
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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 IL1 beta, IL-8, LIF and TGF beta 2.
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页数:14
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