Abstract
The differentiation of helper T cells into effector subsets is critical to host protection. Transcription factors of the E-protein and Id families are important arbiters of T cell development, but their role in the differentiation of the TH1 and TFH subsets of helper T cells is not well understood. Here, TH1 cells showed more robust Id2 expression than that of TFH cells, and depletion of Id2 via RNA-mediated interference increased the frequency of TFH cells. Furthermore, TH1 differentiation was blocked by Id2 deficiency, which led to E-protein-dependent accumulation of effector cells with mixed characteristics during viral infection and severely impaired the generation of TH1 cells following infection with Toxoplasma gondii. The TFH cell-defining transcriptional repressor Bcl6 bound the Id2 locus, which provides a mechanism for the bimodal Id2 expression and reciprocal development of TH1 cells and TFH cells.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, N.I.H., Extramural
MeSH terms
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Animals
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Arenaviridae Infections / immunology*
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Basic Helix-Loop-Helix Transcription Factors / metabolism
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Cell Differentiation*
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Cells, Cultured
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Female
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Germinal Center / immunology
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Inhibitor of Differentiation Protein 2 / genetics
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Inhibitor of Differentiation Protein 2 / metabolism*
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Lymphocytic choriomeningitis virus / immunology*
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Male
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Mice
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Mice, Inbred C57BL
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Mice, Inbred CBA
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Mice, Transgenic
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Protein Binding
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Proto-Oncogene Proteins c-bcl-6 / metabolism
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RNA, Small Interfering / genetics
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Th1 Cells / parasitology
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Th1 Cells / physiology*
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Th1 Cells / virology
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Toxoplasma / immunology*
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Toxoplasmosis / immunology*
Substances
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Basic Helix-Loop-Helix Transcription Factors
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Bcl6 protein, mouse
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Idb2 protein, mouse
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Inhibitor of Differentiation Protein 2
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Proto-Oncogene Proteins c-bcl-6
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RNA, Small Interfering
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Tcf3 protein, mouse