Cytokine regulation of IL-13Rα2 and IL-13Rα1 in vivo and in vitro

Abstract

Background: IL-13 signals via a high-affinity receptor that includes IL-4Rα and IL-13Rα1 and binds to the decoy receptor IL-13Rα2. The processes that regulate the expression of these receptor subunits, however, are poorly defined. Objective: These studies were designed to define the regulation of IL-13R components by T H2 and T H1 cytokines in vivo and in vitro. Methods: Northern analysis, in situ hybridization, RT-PCR analysis, and immunoprecipitation were used to define the expression of IL-13Rα1 and IL-13Rα2 in lungs from lung targeted overexpression mice and lung fragments and cells in culture. Results: IL-13Rα2 and IL-13Rα1 mRNA were detected at modest levels in lungs from control mice. In contrast, transgenic IL-13 caused a marked increase in IL-13Rα2 and IL-13Rα1 mRNA; this was most prominent in airway epithelial cells and macrophages. The effects of IL-13 on IL-13Rα2 were associated with comparable increases in protein production and were mediated by a blood leukocyte–independent and IL-4Rα–dependent mechanism. IL-13 stimulation of IL-13Rα1 was mediated via a blood leukocyte–dependent and partially IL-4Rα–dependent pathway. These effects were not specific for IL-13, because transgenic IL-4, IL-10, and IFN-γ also stimulated IL-13Rα2 mRNA accumulation while stimulating—not altering and inhibiting—IL-13Rα1 mRNA accumulation, respectively. These regulatory events were mediated, at least in part, by direct effects of these cytokines, because IL-13, IL-4, and IFN-γ had similar effects on IL-13Rα2 and/or IL-13Rα1 in epithelial cells and macrophages in in vitro culture. Conclusion: IL-13Rα2 and IL-13Rα1 are highly regulated in vivo and in vitro. These regulatory events might control IL-13 responses at sites of inflammation.