van den Berk Lieke C J, Jansen Bas J H, Snowden Stuart, Siebers-Vermeulen Kim G C, Gilissen Christian, Kögler Gesine, Figdor Carl G, Wheelock Craig E, Torensma Ruurd
1 Department of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre , Nijmegen, The Netherlands .
Stem Cells Dev. 2014 Jul 15;23(14):1582-93. doi: 10.1089/scd.2013.0433. Epub 2014 Apr 23.
Immune suppression is a very stable property of multipotent stromal cells also known as mesenchymal stem cells (MSCs). All cell lines tested showed robust immune suppression not affected by a long culture history. Several mechanisms were described to account for this capability. Since several of the described mechanisms were not causing the immune suppression, the expression pattern of cord-blood-derived MSCs by microarray experiments was determined. Dendritic cells cocultured with cord blood MSCs were compared with cord blood MSCs. Putative immune suppressive candidates were tested to explain this inhibition. We find that cord blood MSCs themselves are hardly immunogenic as tested with allogeneic T-cells. Dendritic cells cocultured with second-party T-cells evoked abundant proliferation that was inhibited by third-party cord blood MSCs. Optimal inhibition was seen with one cord blood MSC for every dendritic cell. Blocking human leukocyte antigen G only saw partial recovery of proliferation. Several cytokines, gangliosides, enzymes like arginase, NO synthase, and indole amine 2,3-dioxygenase as well as the induction of Treg were not involved in the inhibition. The inhibiting moiety was identified as prostaglandin B2 by lipid metabolite analysis of the culture supernatant and confirmed with purified prostaglandin B2.
免疫抑制是多能间充质干细胞(MSCs)非常稳定的特性。所有测试的细胞系均表现出强大的免疫抑制作用,且不受长培养历史的影响。已描述了几种机制来解释这种能力。由于所描述的几种机制并非导致免疫抑制的原因,因此通过微阵列实验确定了脐血来源的间充质干细胞的表达模式。将与脐血间充质干细胞共培养的树突状细胞与脐血间充质干细胞进行比较。对假定的免疫抑制候选物进行测试以解释这种抑制作用。我们发现,用同种异体T细胞测试时,脐血间充质干细胞本身几乎没有免疫原性。与第三方T细胞共培养的树突状细胞引发大量增殖,而第三方脐血间充质干细胞可抑制这种增殖。每一个树突状细胞与一个脐血间充质干细胞共同培养时可见最佳抑制效果。阻断人类白细胞抗原G仅使增殖部分恢复。几种细胞因子、神经节苷脂、诸如精氨酸酶、一氧化氮合酶和吲哚胺2,3-双加氧酶等酶以及调节性T细胞的诱导均未参与抑制作用。通过对培养上清液进行脂质代谢物分析,将抑制部分鉴定为前列腺素B2,并用纯化的前列腺素B2进行了确认。