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Unique pattern of expression and inhibition of IL‐1 signaling by the IL‐1 receptor family member TIR8\SIGIRR Volume 14, issue 4, Oct.-Nov.-Dec.

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Authors
Dept. Immunology and Cell Biology, Mario Negri Institute for Pharmacological Research, Milan, 20157, Italy Current affiliation : Centro de Ingenieria Genetica y Biotecnologia, Havana, Cuba Current affiliation : Dept. Pharmacology, Discovery Research Oncology, Pharmacia corp., Nerviano, Italy Current affiliation : Inst. for Research in Biomedicine, Bellinzona, Switzerland Current affiliation : MolMed S.p.A. Milan, Italy Current affiliation : Dept. Animal Pathology, Hygiene and Public Health, Faculty of Veterinary Medicine, University of Milan, Milano, Italy Dept. Molecular Medicine, Mario Negri Institute for Pharmacological Research, Bergamo, Italy Centro IDET, Institute of General Pathology, Università degli Studi di Milano, Milan, 20100, Italy N.P. and G.P.R. equally contributed to this project

TIR8, also known as single Ig IL‐1R‐related molecule (SIGIRR), is a member of the IL‐1 receptor family. The present study was designed to investigate the expression and function of TIR8. TIR8 was mainly expressed in mouse and human epithelial tissues such as kidney, lung and gut. Resting and activated T and B lymphocytes and monocytes‐macrophages expressed little or no TIR8, with the exception of the mouse GG2EE macrophage line. In the kidney, the organ with highest mRNA levels, TIR8 expression was confined to epithelial cells and, in situ, to tubular epithelium. A variety of signals failed to regulate TIR8 expression, but LPS reduced TIR8 mRNA transcripts. An NF‐kB driven reporter system was used to investigate the function of TIR8. TIR8 did not activate NF‐kB expression alone or in concert with IL‐1R1. In contrast, TIR8 inhibited signaling from the IL‐1R complex. Inhibition required the intracellular portion of TIR8 but the extracellular domain was dispensable for blocking activity. Thus, TIR8 is a unique member of the IL‐1R family, with a distinct pattern of epithelial expression, including the kidney and mucosae, and an inhibitory function on IL‐1 signaling.