A Critical Role for the Innate Immune Signaling Molecule IRAK-4 in T Cell Activation

Author:

Suzuki Nobutaka1234,Suzuki Shinobu1234,Millar Douglas G.1234,Unno Midori1234,Hara Hiromitsu1234,Calzascia Thomas1234,Yamasaki Sho1234,Yokosuka Tadashi1234,Chen Nien-Jung1234,Elford Alisha R.1234,Suzuki Jun-ichiro1234,Takeuchi Arata1234,Mirtsos Christine1234,Bouchard Denis1234,Ohashi Pamela S.1234,Yeh Wen-Chen1234,Saito Takashi1234

Affiliation:

1. Laboratory for Cell Signaling, RIKEN Research Center for Allergy and Immunology, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama City, Kanagawa 230-0045, Japan.

2. Institute for Breast Cancer Research, University Health Network, 620 University Avenue, Suite 706, Toronto, Ontario M5G 2C1, Canada.

3. Advanced Medical Discovery Institute, University Health Network and Department of Medical Biophysics, University of Toronto, 620 University Avenue, Suite 706, Toronto, Ontario M5G 2C1, Canada.

4. Department of Molecular Genetics, Chiba University Graduate School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba City, Chiba 260-8670, Japan.

Abstract

IRAK-4 is a protein kinase that is pivotal in mediating signals for innate immune responses. Here, we report that IRAK-4 signaling is also essential for eliciting adaptive immune responses. Thus, in the absence of IRAK-4, in vivo T cell responses were significantly impaired. Upon T cell receptor stimulation, IRAK-4 is recruited to T cell lipid rafts, where it induces downstream signals, including protein kinase Cθ activation through the association with Zap70. This signaling pathway was found to be required for optimal activation of nuclear factor κB. Our findings suggest that T cells use this critical regulator of innate immunity for the development of acquired immunity, suggesting that IRAK-4 may be involved in direct signal cross talk between the two systems.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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