Immunomodulatory Effects of Human Umbilical Cord Wharton's Jelly-Derived Mesenchymal Stem Cells on Differentiation, Maturation and Endocytosis of Monocyte-Derived Dendritic Cells

被引:1
作者
Saeidi, Mohsen [1 ,2 ]
Masoud, Ahmad [2 ]
Shakiba, Yadollah [2 ]
Hadjati, Jamshid [2 ]
Bonab, Mandana Mohyeddin [2 ]
Nicknam, Mohammad Hossein [2 ,3 ]
Latifpour, Mostafa [4 ]
Nikbin, Behrooz [2 ,3 ]
机构
[1] Golestan Univ Med Sci, Sch Med, Dept Immunol, Gorgan, Iran
[2] Univ Tehran Med Sci, Sch Med, Dept Immunol, Tehran, Iran
[3] Univ Tehran Med Sci, Mol Immunol Res Ctr, Tehran, Iran
[4] Univ Tehran Med Sci, Sch Med, Dept Anat, Tehran, Iran
关键词
Bone marrow; Dendritic cell; Endocytosis; Mesenchymal stem cells; Wharton's jelly; MARROW STROMAL CELLS; HUMAN BONE-MARROW; SURVIVAL IN-VIVO; MATRIX CELLS; IMMUNOLOGICAL FEATURES; ALLOGRAFT SURVIVAL; INHIBIT; PROLIFERATION; VITRO; TOLERANCE;
D O I
暂无
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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 derived-mesenchymal 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-alpha for 2 days. In every stage of differentiation, immature and mature dendritic cells were separately co-cultured 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 cell-cell contacts under laboratory conditions. As DCs are believed to be the main antigen presenting cells for naive 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.
引用
收藏
页码:37 / 49
页数:13
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