Author/Authors :
Saeidi, Mohsen Department of Immunology - School of Medicine - Golestan University of Medical Sciences, Gorgan , Masoud, Ahmad Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Shakiba, Yadollah Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Hadjati, Jamshid Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Mohyeddin Bonab, Mandana Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Nicknam, Mohammad Hossein Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Latifpour, Mostafa Department of Anatomy - School of Medicine - Tehran University of Medical Sciences, Tehran , Nikbin, Behrooz Molecular Immunology Research Center - Tehran University of Medical Sciences, Tehran
Abstract :
The Wharton’s jelly of the umbilical cord is believed to be a source of mesenchymal stem
cells (MSCs) which can be therapeutically applied in degenerative diseases.
In this study, we investigated the immunomodulatory effect of umbilical cord derivedmesenchymal
stem cells (UC-MSCs) and bone marrow-derived-mesenchymal stem cells
(BM-MSCs) on differentiation, maturation, and endocytosis of monocyte-derived dendritic
cells in a transwell culture system under laboratory conditions. Monocytes were differentiated
into immature dendritic cells (iDCs) in the presence of GM-CSF and IL-4 for 6 days and
then differentiated into mature dendritic cells (mDCs) in the presence of TNF-- for 2 days.
In every stage of differentiation, immature and mature dendritic cells were separately cocultured
with UC-MSCs and BM-MSCs.
The findings showed that UC-MSCs and BM-MSCs inhibited strongly differentiation and
maturation of dendritic cells at higher dilution ratios (1:1). The BM-MSCs and UC-MSCs
showed more inhibitory effect on CD1a, CD83, CD86 expression, and dendritic cell
endocytic activity, respectively. On the other hand, these cells severely up-regulated CD14
marker expression.
We concluded that UC-MSCs and BM-MSCs could inhibit differentiation, maturation
and endocytosis in monocyte-derived DCs through the secreted factors and free of any cellcell
contacts under laboratory conditions. As DCs are believed to be the main antigen
presenting cells for naïve T cells in triggering immune responses, it would be logical that
their inhibitory effect on differentiation, maturation and function can decrease or modulate
immune and inflammatory responses.
Keywords :
Bone marrow , Dendritic cell , Endocytosis , Mesenchymal stem cells , Wharton’s jelly