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Publication : Interleukin-17C promotes Th17 cell responses and autoimmune disease via interleukin-17 receptor E.

First Author  Chang SH Year  2011
Journal  Immunity Volume  35
Issue  4 Pages  611-21
PubMed ID  21982598 Mgi Jnum  J:177650
Mgi Id  MGI:5295790 Doi  10.1016/j.immuni.2011.09.010
Citation  Chang SH, et al. (2011) Interleukin-17C Promotes Th17 Cell Responses and Autoimmune Disease via Interleukin-17 Receptor E. Immunity 35(4):611-21
abstractText  Although several interleukin-17 (IL-17) family members and their receptors have been recently appreciated as important regulators in inflammatory diseases, the function of other IL-17 cytokines and IL-17 receptor-like molecules is unclear. Here we show that an IL-17 cytokine family member, IL-17C, was induced in a Th17 cell-dependent autoimmune disease and was required for its pathogenesis. IL-17C bound to IL-17RE, a member of IL-17 receptor family whose full-length isoform was selectively expressed in Th17 cells and signaled via an IL-17RA-RE receptor complex and the downstream adaptor Act1. IL-17C-IL-17RE induced the expression of a nuclear IkappaB family member, IkappaBzeta, in Th17 cells to potentiate the Th17 cell response. Thus, our work has identified a cytokine-receptor pair with important function in regulating proinflammatory responses. This pathway may be targeted to treat autoimmune diseases.
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