Abstract
The inducible costimulatory molecule ICOS has been suggested to be important in the development of interleukin 17 (IL-17)-producing helper T cells (T(H)-17 cells) and of follicular helper T cells (T(FH) cells). Here we show that ICOS-deficient mice had no defect in T(H)-17 differentiation but had fewer T(H)-17 cells after IL-23 stimulation and fewer T(FH) cells. We also show that T(FH) cells produced IL-17 and that T(FH) cells in ICOS-deficient mice were defective in IL-17 production. Both T(H)-17 and T(FH) cells had higher expression of the transcription factor c-Maf. Genetic loss of c-Maf resulted in a defect in IL-21 production and fewer T(H)-17 and T(FH) cells. Thus our data suggest that ICOS-induced c-Maf regulates IL-21 production that in turn regulates the expansion of T(H)-17 and T(FH) cells.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antigens, Differentiation, T-Lymphocyte / genetics
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Antigens, Differentiation, T-Lymphocyte / immunology
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Antigens, Differentiation, T-Lymphocyte / metabolism*
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Cell Differentiation / immunology
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Cell Proliferation
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Encephalomyelitis, Autoimmune, Experimental / immunology
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Enzyme-Linked Immunosorbent Assay
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Flow Cytometry
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Gene Expression Regulation / immunology*
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Inducible T-Cell Co-Stimulator Protein
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Interleukin-17 / immunology
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Interleukin-17 / metabolism
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Interleukins / biosynthesis*
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Interleukins / immunology
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Mice
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Mice, Transgenic
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Oligonucleotide Array Sequence Analysis
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Proto-Oncogene Proteins c-maf / biosynthesis*
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Proto-Oncogene Proteins c-maf / immunology
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Reverse Transcriptase Polymerase Chain Reaction
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T-Lymphocyte Subsets / cytology*
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T-Lymphocyte Subsets / immunology
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T-Lymphocyte Subsets / metabolism
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T-Lymphocytes, Helper-Inducer / cytology*
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T-Lymphocytes, Helper-Inducer / immunology
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T-Lymphocytes, Helper-Inducer / metabolism
Substances
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Antigens, Differentiation, T-Lymphocyte
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Icos protein, mouse
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Inducible T-Cell Co-Stimulator Protein
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Interleukin-17
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Interleukins
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Maf protein, mouse
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Proto-Oncogene Proteins c-maf
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interleukin-21