Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3065348 | Journal of Neuroimmunology | 2008 | 8 Pages |
Abstract
Interleukin (IL)-17-producing helper T cells may play a pivotal role in the pathogenesis of multiple sclerosis. Here, we examined the effects of IL-17 on microglia, which are known to be critically involved in multiple sclerosis. Treatment with IL-17 upregulated the microglial production of IL-6, macrophage inflammatory protein-2, nitric oxide, adhesion molecules, and neurotrophic factors. We also found that IL-17 was produced by microglia in response to IL-23 or IL-1β. Because microglia produce IL-1β and IL-23, these cytokines may act in an autocrine manner to induce IL-17 expression in microglia, and thereby contribute to autoimmune diseases, such as MS, in the central nervous system.
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Authors
Jun Kawanokuchi, Kouki Shimizu, Atsumi Nitta, Kiyofumi Yamada, Tetsuya Mizuno, Hideyuki Takeuchi, Akio Suzumura,