Title of article :
Immunomodulatory Effects of Mice Mesenchymal Stem Cells on Maturation and Activation of Dendritic Cells
Author/Authors :
Sadeghi, Ladan Department of Biology - Islamic Azad University - Fars Science and Research Branch , Kamali-Sarvestani, Eskandar Autoimmune Diseases Research Center and Immunology Department - Shiraz University of Medical Sciences , Azarpira, Negar Transplant Research Center - Shiraz University of Medical Sciences - Shiraz , Karimi, Mohammad Hossein Transplant Research Center - Shiraz University of Medical Sciences - Shiraz , Shariati, Mehrdad Department of Biology - Islamic Azad University - Kazerun branch - Kazerun
Abstract :
Background: Mesenchymal stem cells (MSCs) possess a wide range of
immunomodulatory functions mostly in immune cells including dendritic cells (DCs).
DCs are the key cells in the immune response and play an important role in initiating
cell-mediated immunity. Objective: To evaluate the immunomodulatory effects of
MSCs supernatant on maturation and function of DCs. Methods: Bone marrow derived
mice MSCs were isolated and cultured. Twenty-four, forty-eight and seventy-two hours
after passage 6, supernatants were collected and MSCs were assessed by cytometric
analysis for the expression of CD34, CD44, CD45 and SCA-1. Splenic DCs were
isolated using MACS and then co-cultured with MSCs supernatant. Expression of
CD86, CD40 and MHC-II on DCs were also evaluated by cytometry. H3-thymidine
incorporation by proliferating T cells was determined in two separate MLR assay
settings. In one setting, DCs were co-cultured with T cells in the presence of MSCs
supernatant, and in the other setting DCs were treated with MSCs supernatant and then
were co-cultured with T cells. Production of IL-12, IL-6 and IL-10 cytokines was
measured in the supernatant of DCs treated with MSCs supernatant. We also measured
IFN-γ and IL-4 levels in MLR supernatant. Results: The results showed that 72h MSCs
supernatant could decrease the expression of MHC-II and CD86. The T cell
proliferation was inhibited in the presence of MSCs supernatant and MSCs supernatant
treated DCs as demonstrated by MLR assay. A significant increase in IL-4 level and a
non significant decrease in IFN-γ level in MLR supernatant were observed. However,
IL-6, IL-10 and IL-12 production did not change significantly. Conclusion: MSCs
supernatant has a time dependent effect on the maturation of DCs. Also, it could alter
cytokine production from responding T cells toward Th2. Generally, the findings of this
study supported the immunomodulatory effect of MSCs supernatant on DCs maturation
and function.
Keywords :
DCs , MSCs , Immunomodulation
Journal title :
Astroparticle Physics