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The Journal of Immunology, 2006, 176: 7495-7501.
Copyright © 2006 by The American Association of Immunologists

Level of Expression of IL-13R{alpha}2 Impacts Receptor Distribution and IL-13 Signaling1

Michael O. Daines, Yasuhiro Tabata, Bradley A. Walker, Weiguo Chen, Manoj R. Warrier, Saswata Basu and Gurjit K. Khurana Hershey2

Division of Allergy and Immunology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229

IL-13, a critical cytokine for allergic inflammation, exerts its effects through a complex receptor system including IL-4R{alpha}, IL-13R{alpha}1, and IL-13R{alpha}2. IL-4R{alpha} and IL-13R{alpha}1 form a heterodimeric signaling receptor for IL-13. In contrast, IL-13R{alpha}2 binds IL-13 with high affinity but does not signal. IL-13R{alpha}2 exists on the cell surface, intracellularly, and in soluble form, but no information is available regarding the relative distributions of IL-13R{alpha}2 among these compartments, whether the compartments communicate, and how the relative expression levels impact IL-13 responses. Herein, we investigated the distribution of IL-13R{alpha}2 in transfected and primary cells, and we evaluated how the total level of IL-13R{alpha}2 expression impacted its distribution. Our results demonstrate that the distribution of IL-13R{alpha}2 is independent of the overall level of expression. The majority of the IL-13R{alpha}2 protein existed in intracellular pools. Surface IL-13R{alpha}2 was continually released into the medium in a soluble form, yet surface expression remained constant supporting receptor trafficking to the cell surface. IL-13R{alpha}2 inhibited IL-13 signaling proportionally to its level of expression, and this inhibition could be overcome with high concentrations of IL-13.




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