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Transplant Proc ; 41(1): 403-9, 2009.
Article in English | MEDLINE | ID: mdl-19249567

ABSTRACT

Bone marrow mesenchymal stem cells (MSCs) demonstrate functions of immunologic regulation. However, little is known about the role of interferon-gamma (IFN-gamma) on MSCs and whether MSCs alone can prevent allograft rejection. We purified MSCs, which were or were not treated with IFN-gamma, to act as regulatory cells in mixed lymphocyte reactions. We measured their expression of PDL-1, MHC-I, MHC-II, CD40, CD54, and CD86. The MSCs stained with carboxyfluorescein diacetate-succinimidyl ester were used to detect homing in vivo. The MSCs were injected into an orthotopic liver transplantation model. The result suggested that IFN-gamma enhances expression of PDL-1, MHC-I, MHC-II, and CD54 and boosts immunosuppressive ability in vivo. The MSCs demonstrated homing to the liver, alleviating acute immunologic rejection of an hepatic graft in rats. We conclude that IFN-gamma may enhance the immunosuppressive function of MSCs to protect liver allografts in rats from acute immunologic rejection.


Subject(s)
Bone Marrow Transplantation/immunology , Graft Rejection/immunology , Liver Transplantation/immunology , Mesenchymal Stem Cell Transplantation , Animals , Epitopes/immunology , Female , Flow Cytometry , Gene Expression Regulation , Graft Rejection/prevention & control , Immunosuppression Therapy , Leukocyte Common Antigens/immunology , Male , Rats , Rats, Inbred BN , Sex-Determining Region Y Protein/genetics , Thy-1 Antigens/immunology , Transplantation Chimera , Y Chromosome
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