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Immunomodulatory effects of human umbilical cord wharton's Jelly-Derived mesenchymal stem cells on differentiation, maturation and endocytosis of monocyte-derived dendritic cells

机译:人脐带沃顿氏胶质间充质干细胞对单核细胞来源树突状细胞分化,成熟和内吞作用的免疫调节作用

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 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 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. Copyright © Spring 2013, Iran J Allergy Asthma Immunol. All rights reserved.
机译:脐带的沃顿氏胶被认为是间充质干细胞(MSCs)的来源,可治疗退行性疾病。在这项研究中,我们研究了脐带衍生的间充质干细胞(UC-MSCs)和骨髓源性间充质干细胞(BM-MSCs)对单孔细胞衍生的树突状细胞在分化,分化和成熟及内吞作用中的免疫调节作用。实验室条件下的培养系统。在存在GM-CSF和IL-4的情况下,单核细胞分化为未成熟的树突状细胞(iDC)6天,然后在存在TNF-的情况下分化为成熟的树突状细胞(mDCs)2天。在分化的每个阶段,将未成熟和成熟的树突状细胞分别与UC-MSC和BM-MSC共培养。研究结果表明,UC-MSC和BM-MSC在较高的稀释比(1:1)下可抑制树突状细胞的强烈分化和成熟。 BM-MSC和UC-MSC分别对CD1a,CD83,CD86表达和树突状细胞内吞活性具有更大的抑制作用。另一方面,这些细胞严重上调了CD14标志物的表达。我们得出的结论是,UC-MSC和BM-MSC可以通过分泌因子抑制单核细胞衍生DC的分化,成熟和内吞作用,并且在实验室条件下不存在任何细胞接触。由于DC被认为是幼稚T细胞触发免疫反应的主要抗原呈递细胞,因此逻辑上它们对分化,成熟和功能的抑制作用可以减少或调节免疫和炎性反应是合乎逻辑的。版权所有©2013年春季,伊朗J过敏性哮喘免疫。版权所有。

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