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Notch1 modulates mesenchymal stem cells mediated regulatory T-cell induction

机译:Notch1调节间充质干细胞介导的调节t细胞诱导

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摘要

Notch1 signaling is involved in regulatory T (Treg)-cell differentiation. We previously demonstrated that, when cocultured with CD3+ cells, mesenchymal stem cells (MSCs) induced a T-cell population with a regulatory phenotype. Here, we investigated the molecular mechanism underlying MSC induction of human Treg cells. We show that the Notch1 pathway is activated in CD4+ T cells cocultured with MSCs. Inhibition of Notch1 signaling through GSI-I or the Notch1 neutralizing antibody reduced expression of HES1 (the Notch1 downstream target) and the percentage of MSC-induced CD4+CD25highFOXP3+ cells in vitro. Moreover, we demonstrate that FOXP3 is a downstream target of Notch signaling in human cells. No crosstalk between Notch1 and TGF-β signaling pathways was observed in our experimental system. Together, these findings indicate that activation of the Notch1 pathway is a novel mechanism in the human Treg-cell induction mediated by MSCs.
机译:Notch1信号参与调节性T(Treg)细胞分化。表明,当cocultured CD3 +细胞、间充质干细胞(msc)诱导t细胞数量与监管表型。在这里,我们调查的分子机制潜在的MSC诱导人类Treg细胞。表明,CD4 + Notch1通路被激活T细胞cocultured msc。通过GSI-I或Notch1 Notch1信号中和抗体减少HES1的表情(Notch1下游目标)和百分比MSC-induced CD4 + CD25highFOXP3 +细胞体外。此外,我们证明具体下游Notch信号在人类的目标细胞。信号通路在我们观察到实验系统。表明Notch1通路的激活一个新颖的机制在人类Treg-cell归纳由msc。

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