Literature DB >> 18286567

IRAK-4 kinase activity is required for IRAK-4-dependent innate and adaptive immune responses.

Elizabeth Lye1, Salim Dhanji, Thomas Calzascia, Alisha R Elford, Pamela S Ohashi.   

Abstract

Interleukin-1 receptor-associated kinase (IRAK)-4 is a serine-threonine kinase that plays an important role in innate and adaptive immune responses. While the requirement of IRAK-4 kinase activity has been studied in the context of IL-1R signaling, it is not clear whether IRAK-4 requires its kinase function for all of its roles in the immune system. IRAK-4 kinase-dead knock-in (IRAK-4KD/KD) mice were generated to further elucidate whether IRAK-4 kinase activity is required for IRAK-4 to induce cytokine production. IRAK-4KD/KD mice were impaired in their ability to produce cytokines in response to in vivo challenge with lipopolysaccharide (LPS), a potent TLR4 ligand. Cytokine production was also reduced in macrophages and dendritic cells from IRAK-4KD/KD mice in response to LPS and other TLR ligands. In addition, adaptive immune responses were impaired in IRAK-4KD/KD mice. Although in vitro T cell proliferation in response to TCR activation was unaffected in IRAK-4-deficient mice, in vivo T cell responses to lymphocytic choriomeningitits virus infection were significantly impaired in IRAK-4-knockout mice or mice expressing the kinase-dead mutant of IRAK-4. Collectively, these results indicate that IRAK-4 kinase activity is required for IRAK-4-dependent signaling in innate and adaptive immunity.

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Year:  2008        PMID: 18286567     DOI: 10.1002/eji.200737429

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  19 in total

1.  Interleukin-1R signaling is essential for induction of proapoptotic CD8 T cells, viral clearance, and pathology during lymphocytic choriomeningitis virus infection in mice.

Authors:  Lars T Joeckel; Reinhard Wallich; Sunil S Metkar; Christopher J Froelich; Markus M Simon; Christoph Borner
Journal:  J Virol       Date:  2012-06-06       Impact factor: 5.103

2.  IRAK4 kinase activity is not required for induction of endotoxin tolerance but contributes to TLR2-mediated tolerance.

Authors:  Yanbao Xiong; Meghan Pennini; Stefanie N Vogel; Andrei E Medvedev
Journal:  J Leukoc Biol       Date:  2013-05-21       Impact factor: 4.962

3.  Induction of endotoxin tolerance in vivo inhibits activation of IRAK4 and increases negative regulators IRAK-M, SHIP-1, and A20.

Authors:  Yanbao Xiong; Andrei E Medvedev
Journal:  J Leukoc Biol       Date:  2011-09-20       Impact factor: 4.962

4.  Impaired T-cell receptor activation in IL-1 receptor-associated kinase-4-deficient patients.

Authors:  Douglas R McDonald; Frederick Goldman; Oscar D Gomez-Duarte; Andrew C Issekutz; Dinakantha S Kumararatne; Rainer Doffinger; Raif S Geha
Journal:  J Allergy Clin Immunol       Date:  2010-08       Impact factor: 10.793

5.  Conformational flexibility and inhibitor binding to unphosphorylated interleukin-1 receptor-associated kinase 4 (IRAK4).

Authors:  Li Wang; Ryan Ferrao; Qiubai Li; John M Hatcher; Hwan Geun Choi; Sara J Buhrlage; Nathanael S Gray; Hao Wu
Journal:  J Biol Chem       Date:  2019-01-24       Impact factor: 5.157

6.  Deficiency in IRAK4 activity attenuates manifestations of murine Lupus.

Authors:  Michael Murphy; Goutham Pattabiraman; Tissa T Manavalan; Andrei E Medvedev
Journal:  Eur J Immunol       Date:  2017-03-31       Impact factor: 5.532

7.  Complete dependence on IRAK4 kinase activity in TLR2, but not TLR4, signaling pathways underlies decreased cytokine production and increased susceptibility to Streptococcus pneumoniae infection in IRAK4 kinase-inactive mice.

Authors:  Meghan E Pennini; Darren J Perkins; Andres M Salazar; Michael Lipsky; Stefanie N Vogel
Journal:  J Immunol       Date:  2012-12-03       Impact factor: 5.422

8.  Differential role for c-Rel and C/EBPbeta/delta in TLR-mediated induction of proinflammatory cytokines.

Authors:  Yong-Chen Lu; Ira Kim; Elizabeth Lye; Fang Shen; Nobutaka Suzuki; Shinobu Suzuki; Steve Gerondakis; Shizuo Akira; Sarah L Gaffen; Wen-Chen Yeh; Pamela S Ohashi
Journal:  J Immunol       Date:  2009-06-01       Impact factor: 5.422

Review 9.  Suppressors of cytokine signaling (SOCS) in T cell differentiation, maturation, and function.

Authors:  Douglas C Palmer; Nicholas P Restifo
Journal:  Trends Immunol       Date:  2009-10-30       Impact factor: 16.687

10.  MAP kinase phosphatase-1, a critical negative regulator of the innate immune response.

Authors:  Liwu Li; Shuang-Feng Chen; Yusen Liu
Journal:  Int J Clin Exp Med       Date:  2009-02-15
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