Most cited article - PubMed ID 21903294
IL-12 inhibits the TGF-β-dependent T cell developmental programs and skews the TGF-β-induced differentiation into a Th1-like direction
Regulatory T cells have been well described and the factors regulating their development and function have been identified. Recently, a growing body of evidence has documented the existence of interleukin-10 (IL-10) -producing B cells, which are called regulatory B10 cells. These cells attenuate autoimmune, inflammatory and transplantation reactions, and the main mechanism of their inhibitory action is the production of IL-10. We show that the production of IL-10 by lipopolysaccharide-stimulated B cells is significantly enhanced by IL-12 and interferon-γ and negatively regulated by IL-21 and transforming growth factor-β. In addition, exogenous IL-10 also inhibits B-cell proliferation and the expression of the IL-10 gene in lipopolysaccharide-stimulated B cells. The negative autoregulation of IL-10 production is supported by the observation that the inclusion of anti-IL-10 receptor monoclonal antibody enhances IL-10 production and the proliferation of activated B cells. The effects of cytokines on IL-10 production by B10 cells did not correlate with their effects on B-cell proliferation or on IL-10 production by T cells or macrophages. The cytokine-induced changes in IL-10 production occurred on the level of IL-10 gene expression, as confirmed by increased or decreased IL-10 mRNA expression in the presence of a particular cytokine. The regulatory cytokines modulate the number of IL-10-producing cells rather than augmenting or decreasing the secretion of IL-10 on a single-cell level. Altogether these data show that the production of IL-10 by B cells is under the strict regulatory control of cytokines and that individual cytokines differentially regulate the development and activity of regulatory T cells and IL-10-producing regulatory B cells.
- Keywords
- B cells, autoregulation, cytokines, immunosuppression, interleukin-10 production,
- MeSH
- Lymphocyte Activation MeSH
- Cell Differentiation * drug effects MeSH
- Cytokines genetics metabolism MeSH
- Homeostasis MeSH
- Interferon-gamma metabolism MeSH
- Interleukin-10 genetics metabolism MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Lipopolysaccharides pharmacology MeSH
- RNA, Messenger metabolism MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Cell Proliferation MeSH
- Gene Expression Regulation MeSH
- B-Lymphocytes, Regulatory drug effects immunology metabolism MeSH
- T-Lymphocytes, Regulatory immunology metabolism MeSH
- Recombinant Proteins metabolism MeSH
- Signal Transduction MeSH
- Tumor Necrosis Factor-alpha metabolism MeSH
- Transforming Growth Factor beta1 metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cytokines MeSH
- IFNG protein, human MeSH Browser
- IL10 protein, mouse MeSH Browser
- Interferon-gamma MeSH
- Interleukin-10 MeSH
- Lipopolysaccharides MeSH
- RNA, Messenger MeSH
- Recombinant Proteins MeSH
- TGFB1 protein, human MeSH Browser
- Tumor Necrosis Factor-alpha MeSH
- Transforming Growth Factor beta1 MeSH