T cell-expressed microRNAs critically regulate germinal center T follicular helper cell function and maintenance in acute viral infection in mice |
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Authors: | Julia Zeiträg Frank Dahlström Yinshui Chang Dominik Alterauge Daniel Richter Julia Niemietz Dirk Baumjohann |
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Affiliation: | 1. Institute for Immunology, Biomedical Center, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Germany;2. Anthropology and Human Genomics, Department Biology II, Faculty of Biology, LMU Munich, Planegg-Martinsried, Germany |
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Abstract: | Constitutive T cell-intrinsic miRNA expression is required for the differentiation of naïve CD4+ T cells into Tfh cells, thus making it difficult to study the role of miRNAs in the maintenance of already established Tfh cells and ongoing germinal center (GC) responses. To overcome this problem, we here used temporally controlled ablation of mature miRNAs specifically in CD4+ T cells during acute LCMV infection in mice. T cell-intrinsic miRNA expression was not only critical at early stages of Tfh cell differentiation, but also important for the maintenance of already established Tfh cells. In addition, CD4+ T cell-specific ablation of miRNAs resulted in impaired GC B cell responses. Notably, miRNA deficiency also compromised the antigen-specific CD4+ T cell compartment, Th1 cells, Treg cells, and Tfr cells. In conclusion, our results highlight miRNAs as important regulators of Tfh cells, thus providing novel insights into the molecular events that govern T cell–B cell interactions and Th cell identity. |
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Keywords: | Th cells T follicular helper cells microRNA germinal center Dgcr8 |
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