Abstract
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(+) CD25(high) FOXP3(+) 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.
© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antibodies, Blocking / pharmacology
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Basic Helix-Loop-Helix Transcription Factors / genetics
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Basic Helix-Loop-Helix Transcription Factors / metabolism
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CD4 Antigens / metabolism
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Cell Differentiation
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Cells, Cultured
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Coculture Techniques
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Forkhead Transcription Factors / genetics
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Forkhead Transcription Factors / metabolism*
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Gene Expression Regulation / drug effects
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Gene Expression Regulation / immunology
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Homeodomain Proteins / genetics
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Homeodomain Proteins / metabolism
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Humans
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Interleukin-2 Receptor alpha Subunit / metabolism
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Lymphocyte Count
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Mesenchymal Stem Cells / drug effects
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Mesenchymal Stem Cells / immunology*
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Oligopeptides / pharmacology
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Receptor, Notch1 / antagonists & inhibitors
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Receptor, Notch1 / immunology
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Receptor, Notch1 / metabolism*
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Signal Transduction / drug effects
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T-Lymphocyte Subsets / drug effects
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T-Lymphocyte Subsets / immunology*
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T-Lymphocytes, Regulatory / drug effects
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T-Lymphocytes, Regulatory / immunology*
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Transcription Factor HES-1
Substances
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Antibodies, Blocking
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Basic Helix-Loop-Helix Transcription Factors
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CD4 Antigens
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FOXP3 protein, human
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Forkhead Transcription Factors
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Homeodomain Proteins
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Interleukin-2 Receptor alpha Subunit
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Oligopeptides
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Receptor, Notch1
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Transcription Factor HES-1
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benzyloxycarbonyl-leucyl-leucyl-norleucinal
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HES1 protein, human