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Cutting Edge: IL-26 Signals through a Novel Receptor Complex Composed of IL-20 Receptor 1 and IL-10 Receptor 2
Author(s) -
Faruk Sheikh,
Vitaliy V. Baurin,
Anita Lewis-Antes,
Nital K. Shah,
Smirnov Sv,
Shubha Anantha,
Harold Dickensheets,
Laure Dumoutier,
JeanChristophe Renauld,
Alexander Zdanov,
Raymond P. Donnelly,
Sergei V. Kotenko
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.172.4.2006
Subject(s) - receptor , interleukin 21 receptor , biology , microbiology and biotechnology , interleukin 4 receptor , signal transduction , cytokine receptor , interleukin 6 receptor , cytokine , interleukin , immunology , biochemistry
The receptor for IL-26 (AK155), a cytokine of the IL-10 family, has not previously been defined. We demonstrate that the active receptor complex for IL-26 is a heterodimer composed of two receptor proteins: IL-20R1 and IL-10R2. Signaling through the IL-26R results in activation of STAT1 and STAT3 which can be blocked by neutralizing Abs against IL-20R1 or IL-10R2. IL-10R2 is broadly expressed on a wide variety of tissues, whereas only a limited number of tissues express IL-20R1. Therefore, the ability to respond to IL-26 is restricted by the expression of IL-20R1. IL-10, IL-19, IL-20, IL-22, and IL-24 fail to signal through the combination of IL-10R2 and IL-20R1 proteins, demonstrating that this receptor combination is unique and specific for IL-26.

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