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Mesenchymal Stem Cells Increase Skin Graft Survival Time and Up-Regulate Pd-L1 Expression in Splenocytes of Mice Publisher Pubmed



Moravej A1, 2 ; Geramizadeh B1 ; Azarpira N1 ; Zarnani AH3, 4 ; Yaghobi R1 ; Kalani M5 ; Khosravi M1 ; Kouhpayeh A2 ; Karimi MH1
Authors
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Authors Affiliations
  1. 1. Transplant Research Center, Nemazee Hospital, Shiraz University of Medical Sciences, Shiraz, Iran
  2. 2. Noncommunicable Diseases Research Centre, Fasa University of Medical Sciences, Fasa, Iran
  3. 3. Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Immunology Research Center, Iran University of Medical Sciences, Tehran, Iran
  5. 5. Alborzi Clinical Microbiology Research Center, Nemazee Hospital, Shiraz University of Medical Sciences, Shiraz, Iran

Source: Immunology Letters Published:2017


Abstract

Recently, mesenchymal stem cells (MSCs) have gained considerable interests as hopeful therapeutic cells in transplantation due to their immunoregulatory functions. But exact mechanisms underlying MSCs immunoregulatory function is not fully understood. Herein, in addition to investigate the ability of MSCs to prolong graft survival time, the effects of them on the expression of PD-L1 and IDO immunomodulatory molecules in splenocytes of skin graft recipient mice was clarified. To achieve this goal, full-thickness skins were transplanted from C57BL/6 to BALB/c mice. MSCs were isolated from bone marrow of BALB/c mice and injected to the recipient mice. Skin graft survival was monitored daily to determine graft rejection time. On days 2, 5 and 10 post skin transplantation, serum cytokine levels and expression of PD-L1 and IDO mRNA and protein in the splenocytes of recipient mice were evaluated. The results showed that administration of MSCs prolonged skin graft survival time from 11 to 14 days. On days 2 and 5 post transplantation, splenocytes PD-L1 expression and IL-10 serum level in MSCs treated mice were higher than those in the controls, while IL-2 and IFN-γ levels were lower. Rejection in MSCs treated mice was accompanied by an increase in IL-2 and IFN-γ, and decrease in PD-L1 expression and IL-10 level. No difference in the expression of IDO between MSCs treated mice and controls was observed. In conclusion, we found that one of the mechanisms underlying MSCs immunomodulatory function could be up-regulating PD-L1 expression. © 2017 European Federation of Immunological Societies