Immunoreceptor tyrosine-based inhibitory motif of the IL-4 receptor associates with SH2-containing phosphatases and regulates IL-4-induced proliferation

M. Kashiwada, C. C. Giallourakis, P. Y. Pan, P. B. Rothman

Research output: Contribution to journalArticlepeer-review

48 Scopus citations

Abstract

Immunoreceptor tyrosine-based inhibitory motifs (ITIM) have been implicated in the negative modulation of immunoreceptor signaling pathways. The IL-4R α-chain (IL-4Rα) contains a putative ITIM in the carboxyl terminal. To determine the role of ITIM in the IL-4 signaling pathway, we ablated the ITIM of IL-4Rα by deletion and site-directed mutagenesis and stably expressed the wild-type (WT) and mutant hIL-4Rα in 32D/insulin receptor substrate-2 (IRS-2) cells. Strikingly, 32D/IRS-2 cells expressing mutant human (h)IL-4Rα were hyperproliferative in response to IL-4 compared with cells expressing WT hIL-4Rα. Enhanced tyrosine phosphorylation of Stat6, but not IRS-2, induced by hIL-4 was observed in cells expressing mutant Y713F. Using peptides corresponding to the ITIM of hIL-4Rα, we demonstrate that tyrosine-phosphorylated peptides, but not their nonphosphorylated counterparts, coprecipitate SH2-containing tyrosine phosphatase-1, SH2-containing tyrosine phosphatase-2, and SH2-containing inositol 5′-phosphatase. The in vivo association of SH2-containing inositol 5′-phosphatase with IL-4Rα was verified by coimmunoprecipitation with anti-IL-4Rα Abs. These results demonstrate a functional role for ITIM in the regulation of IL-4-induced proliferation.

Original languageEnglish (US)
Pages (from-to)6382-6387
Number of pages6
JournalJournal of Immunology
Volume167
Issue number11
DOIs
StatePublished - Dec 1 2001

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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