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10.3727/000000006780666957

http://scihub22266oqcxt.onion/10.3727/000000006780666957
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C6032462!6032462 !17605296
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suck abstract from ncbi


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pmid17605296
      Gene+Expr 2007 ; 13 (4-5 ): 217-26
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  • Identification of IL-10 and TGF-beta transcripts involved in the inhibition of T-lymphocyte proliferation during cell contact with human mesenchymal stem cells #MMPMID17605296
  • Nasef A ; Chapel A ; Mazurier C ; Bouchet S ; Lopez M ; Mathieu N ; Sensebé L ; Zhang Y ; Gorin NC ; Thierry D ; Fouillard L
  • Gene Expr 2007[]; 13 (4-5 ): 217-26 PMID17605296 show ga
  • Mesenchymal stem cells (MSC) inhibit the response of allogeneic T lymphocytes in culture. Because the mechanisms of this effect may differ according to the existence of cell contact, we investigated the differences in gene expression of inhibitory molecules during MSC-T lymphocyte coculture when cell contact does and does not occur. Human MSC and T lymphocytes were cultured together in standard and transwell cultures. MSC gene expression was analyzed by semiquantitative real-time RT-PCR. MSC elicited a high dose-dependent inhibition of T lymphocytes in cultures with cell contact, but inhibition occurred even without cell contact. In both cases, we observed significant upregulation of IDO, LIF, and HLA-G, along with downregulation of HGF and SDF1. In cultures with cell contact, IL-10 and TGF-beta transcripts were expressed in a significantly higher level than in cultures without this contact. Furthermore, in the latter, the increased inhibition of T-cell proliferation was positively correlated with IDO gene expression and negatively correlated with SDF1 gene expression. MSC appear to induce T-cell tolerance by two distinct mechanisms. The first of these, which does not require cell contact, induces expression of the tolerogenic genes IDO, LIF, and HLA-G. The second mechanism, which is contact dependent, modulates IL-10 and TGF-beta gene expression. These two mechanisms probably play separate roles in MSC-induced tolerance in allogeneic hematopoietic stem cell transplantation.
  • |*Gene Expression Regulation [MESH]
  • |Cell Adhesion Molecules/metabolism [MESH]
  • |Cell Communication/*physiology [MESH]
  • |Cell Culture Techniques [MESH]
  • |Cell Proliferation [MESH]
  • |Cells, Cultured [MESH]
  • |Chemokine CXCL12 [MESH]
  • |Chemokines, CXC/metabolism [MESH]
  • |Coculture Techniques [MESH]
  • |Humans [MESH]
  • |Immunosuppression Therapy [MESH]
  • |Interleukin-10/genetics/*metabolism [MESH]
  • |Mesenchymal Stem Cells/cytology/*physiology [MESH]
  • |T-Lymphocytes/cytology/*physiology [MESH]


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