Notch1 modulates mesenchymal stem cells mediated regulatory T-cell induction

被引:66
作者
Del Papa, Beatrice [1 ]
Sportoletti, Paolo [1 ]
Cecchini, Debora [1 ]
Rosati, Emanuela [3 ]
Balucani, Chiara [1 ]
Baldoni, Stefano [1 ]
Fettucciari, Katia [3 ]
Marconi, Pierfrancesco [3 ]
Martelli, Massimo F. [1 ]
Falzetti, Franca [1 ]
Di Ianni, Mauro [1 ,2 ]
机构
[1] Univ Perugia, Hematol & Clin Immunol Sect, Dept Clin & Expt Med, I-06100 Perugia, Italy
[2] Univ Aquila, Chair Hematol, Dept Internal Med & Publ Hlth, I-67100 Laquila, Italy
[3] Univ Perugia, Gen Pathol & Immunol Sect, Dept Clin & Expt Med, I-06100 Perugia, Italy
关键词
Immune regulation; Mesenchymal stem cells; Notch1; Tolerance; Treg cells; TGF-BETA; GATA3; EXPRESSION; GENERATION; FOXP3; DIFFERENTIATION; OVEREXPRESSION; ANTIGEN; CD4(+); LIGAND;
D O I
10.1002/eji.201242643
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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-beta 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.
引用
收藏
页码:182 / 187
页数:6
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