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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Günther, Sebastian Sundberg, Eric J. |
| Description | Author Affiliation: Günther S ( Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201); Sundberg EJ ( Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201) |
| Abstract | The IL-1 family consists of 11 cytokines that control a complex network of proinflammatory signals critical for regulating immune responses to infections. They also play a central role in numerous chronic inflammatory disorders. Accordingly, inhibiting the activities of these cytokines is an important therapeutic strategy for treating autoimmune diseases and lymphomas. Agonist cytokines in the IL-1 family activate signaling by binding their cognate receptor and then recruiting a receptor accessory protein. Conversely, antagonist cytokines bind their cognate receptor but prohibit recruitment of receptor accessory protein, which precludes functional signaling complexes. The IL-36 subfamily of cytokines is the most diverse, including three agonists and at least one antagonist, and is the least well-characterized group within this family. Signaling through the IL-36 receptor directly stimulates dendritic cells and primes naive CD4 T cells for Th1 responses. Appropriately balanced IL-36 signaling is a critical determinant of skin and lung health. IL-36 signaling has been presumed to function analogously to IL-1 signaling. In this study, we have defined molecular determinants of agonist and antagonist signaling through the IL-36 receptor. We present the crystal structure of IL-36γ, which, to our knowledge, is the first reported structure of an IL-36 agonist. Using this structure as a guide, we designed a comprehensive series of IL-36 agonist/antagonist chimeric proteins for which we measured binding to the IL-36 receptor/IL-1 receptor accessory protein complex and functional activation and inhibition of signaling. Our data reveal how the fine specificity of IL-36 signaling is distinct from that of IL-1. |
| ISSN | 00221767 |
| e-ISSN | 15506606 |
| Journal | The Journal of Immunology |
| Issue Number | 2 |
| Volume Number | 193 |
| Language | English |
| Publisher | The American Association of Immunologists |
| Publisher Date | 2014-07-15 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Interleukin-1 Pharmacology Receptors, Interleukin Agonists Antagonists & Inhibitors Amino Acid Sequence Binding Sites Genetics Crystallography, X-ray Hek293 Cells Chemistry Models, Molecular Molecular Sequence Data Mutation Protein Binding Protein Multimerization Protein Structure, Secondary Protein Structure, Tertiary Receptors, Interleukin-1 Metabolism Recombinant Fusion Proteins Sequence Homology, Amino Acid Research Support, Non-u.s. Gov't Research Support, U.s. Gov't, Non-p.h.s. Discipline Immunology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Immunology and Allergy Immunology |
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