نتایج جستجو برای: irak 1

تعداد نتایج: 2753079  

Journal: :Molecular medicine 2012
Jacobien J Hoogerwerf Gerritje J W van der Windt Dana C Blok Arie J Hoogendijk Alex F De Vos Cornelis van 't Veer Sandrine Florquin Koichi S Kobayashi Richard A Flavell Tom van der Poll

Pneumonia is a common cause of morbidity and mortality and the most frequent source of sepsis. Bacteria that try to invade normally sterile body sites are recognized by innate immune cells through pattern recognition receptors, among which toll-like receptors (TLRs) feature prominently. Interleukin-1 receptor (IL-1R)-associated kinase (IRAK)-M is a proximal inhibitor of TLR signaling expressed ...

Journal: :Molecular & cellular proteomics : MCP 2007
Constantinos Brikos Robin Wait Shajna Begum Luke A J O'Neill Jeremy Saklatvala

We investigated the composition of the endogenous ligand-bound type I interleukin-1 (IL-1) receptor (IL-1RI) signaling complex using immunoprecipitation and tandem mass spectrometry. Three proteins with approximate molecular masses of 60 (p60), 36 (p36), and 90 kDa (p90) became phosphorylated after treatment with IL-1. Phosphorylation in vitro of p60 has been reported previously, but its identi...

2014
Qiyuan Tan Monika Majewska-Szczepanik Xiaojun Zhang Marian Szczepanik Zhiguang Zhou F. Susan Wong Li Wen

Type 1 diabetes mellitus (T1DM) is an organ-specific autoimmune disease characterized by progressive destruction of insulin-secreting pancreatic β-cells. Both T-cell-mediated adaptive responses as well as innate immune processes are involved in pathogenesis. Interleukin-1 receptor-associated kinase M (IRAK-M) can effectively inhibit the MyD88 downstream signals in Toll-like receptor pathways, w...

Journal: :Journal of immunology 2009
Pranoti Mandrekar Shashi Bala Donna Catalano Karen Kodys Gyongyi Szabo

Impaired host defense after alcohol use is linked to altered cytokine production, however, acute and chronic alcohol differently modulate monocyte/macrophage activation. We hypothesized that in human monocytes, acute alcohol induces hyporesponsiveness to LPS, resulting in decreased TNF-alpha, whereas chronic alcohol increases TNF-alpha by sensitization to LPS. We found that acute alcohol increa...

Journal: :PLoS Neglected Tropical Diseases 2008
Issa Abu-Dayyeh Marina Tiemi Shio Shintaro Sato Shizuo Akira Benoit Cousineau Martin Olivier

Parasites of the Leishmania genus can rapidly alter several macrophage (MØ) signalling pathways in order to tame down the innate immune response and inflammation, therefore favouring their survival and propagation within their mammalian host. Having recently reported that Leishmania and bacterial LPS generate a significantly stronger inflammatory response in animals and phagocytes functionally ...

Journal: :Journal of immunology 2006
Shilpa Oak Pranoti Mandrekar Donna Catalano Karen Kodys Gyongyi Szabo

Most pathogens express ligands for multiple TLRs that share common downstream signaling. In this study, we investigated the effects of acute alcohol on inflammatory pathways induced by TLR2 or TLR4 ligands and their combination. In human monocytes, alcohol attenuated TLR4- but not TLR2-induced TNF-alpha protein and mRNA levels and NF-kappaB activation. In contrast, acute alcohol augmented TNF-a...

2010
Leah L.N. Hubbard Bethany B. Moore

Antigen presenting cells (APCs) of the innate immune system sense a wide range of pathogens via pattern recognition receptors (PRRs). Engagement of certain PRRs can induce production of pro-inflammatory mediators that facilitate effective clearance of pathogen. Toll-like receptors (TLRs) are a well described group of PRRs that belong to the TLR/Interleukin-1 receptor (IL-1R) superfamily. Howeve...

Journal: :The Journal of Experimental Medicine 2005
Satoshi Uematsu Shintaro Sato Masahiro Yamamoto Tomonori Hirotani Hiroki Kato Fumihiko Takeshita Michiyuki Matsuda Cevayir Coban Ken J. Ishii Taro Kawai Osamu Takeuchi Shizuo Akira

Toll-like receptors (TLRs) recognize microbial pathogens and trigger innate immune responses. Among TLR family members, TLR7, TLR8, and TLR9 induce interferon (IFN)-alpha in plasmacytoid dendritic cells (pDCs). This induction requires the formation of a complex consisting of the adaptor MyD88, tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6) and IFN regulatory factor (IRF) 7. He...

Journal: :European journal of immunology 2008
Magdalena Koziczak-Holbro Anton Glück Claude Tschopp John C Mathison Hermann Gram

IRAK-4 kinase inactive (IRAK-4 KD) knock-in mice display defects in TLR- and IL-1 receptor signaling and are resistant to LPS-induced shock. In the present study we examined the LPS-induced response in IRAK-4 KD mice in more detail. We show that IRAK-4 kinase activity is required for certain aspects of TLR-mediated signaling but not for others. We found that IRAK-4 KD cells displayed reduced JN...

Journal: :The Journal of Experimental Medicine 2003
Andrei E. Medvedev Arnd Lentschat Douglas B. Kuhns Jorge C.G. Blanco Cindy Salkowski Shuling Zhang Moshe Arditi John I. Gallin Stefanie N. Vogel

We identified previously a patient with recurrent bacterial infections who failed to respond to gram-negative LPS in vivo, and whose leukocytes were profoundly hyporesponsive to LPS and IL-1 in vitro. We now demonstrate that this patient also exhibits deficient responses in a skin blister model of aseptic inflammation. A lack of IL-18 responsiveness, coupled with diminished LPS and/or IL-1-indu...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید