◀ Back to TLR4
NOS2 — TLR4
Pathways - manually collected, often from reviews:
-
KEGG Leishmaniasis:
TLR2/TLR4
→
NOS2
(protein-protein, activation)
Text-mined interactions from Literome
Brightbill et al., Science 1999
:
Several lipoproteins stimulated
TLR dependent transcription of inducible
nitric oxide synthase and the production of nitric oxide, a powerful microbicidal pathway
Frost et al., Am J Physiol Cell Physiol 2004
(MAP Kinase Signaling System) :
These data indicate that LPS increases
NOS2 mRNA expression in muscle via a
TLR4 dependent mechanism
Suliman et al., FASEB J 2005
:
In wild-type ( Wt ) mice injected with heat inactivated E. coli, hepatic TLR4 and TLR2 proteins were up-regulated with
TLR dependent increases in transcript levels for tumor necrosis factor ( TNF-alpha ), interleukin 6,
nitric oxide synthase-II ( iNOS ), and NADPH oxidase 2 (Nox2) ... A critical role in the mtDNA damage was determined for
TLR4 mediated
iNOS transcription through the MyD88 pathway
Lee et al., Biochem Pharmacol 2005
:
Together, these results demonstrate that STKs play a positive regulatory role in
TLR4 mediated
iNOS expression in a MyD88 independent ( TRIF dependent ) manner
Copin et al., J Immunol 2007
(Brucellosis) :
Using genetically deficient mice, we demonstrated that the induction of
iNOS and IFN-gamma producing cells due to Brucella infection
required TLR4 and TLR9 stimulation coupled to Myd88 dependent signaling pathways
Uno et al., Am J Physiol Gastrointest Liver Physiol 2007
(Helicobacter Infections) :
The induction of
iNOS and the associated nitric oxide production in response to H. pylori-LPS stimulation were
inhibited by declines in not only
TLR4 but also TLR2
Tsukamoto et al., J Immunol 2008
:
Previous pharmacologic studies have suggested that a PI3K-Akt pathway negatively regulates
TLR induced
inducible NO synthase expression and cytokine production
Masamune et al., J Gastroenterol 2008
:
TLR ligands
induced expression of monocyte chemoattractant protein 1, cytokine induced neutrophil chemoattractant 1 ( a rat homolog of interleukin-8 ), and inducible
nitric oxide synthase , but not proliferation or type I collagen production
Zhang et al., J Neuroimmunol 2010
:
In LPS treated primary SCs, retreatment with PPAR-gamma agonist remitted the increase of
iNOS , p38 phosphorylation and
TLR4 , MyD88,
augmented the expression of PPAR-gamma and localization in nuclear
Lin et al., Mol Immunol 2010
:
Nevertheless
TLR mediated JNK activation as well as the increased protein expression of
iNOS and COX-2 remained unchanged when Syk protein was knockdown by siRNA approach
Shweash et al., Mol Immunol 2011
(Leishmaniasis) :
Leishmania mexicana promastigotes inhibit macrophage IL-12 production via
TLR-4 dependent COX-2,
iNOS and arginase-1 expression ... Induction of COX-2 and
iNOS was also
TLR-4 dependent ... These data demonstrate for the first time the
role of
TLR-4 in mediating the effects of L. mexicana promastigotes on MAP kinase activation, up-regulation of COX-2,
iNOS as well as arginase-1 expression in macrophages and further shows that PGE ( 2 ), NO and arginase activity all contribute substantially to the inhibition of host cell IL-12 production
Peng et al., Acta Biochim Biophys Sin (Shanghai) 2012
(Inflammation) :
TLR4 inhibition
reduced LPS induced upregulation of
inducible nitric oxide synthase (iNOS) and ICAM-1 as well as PARP1
Brieger et al., J Immunol 2013
:
Chelation of Zn ( 2+ ) with the membrane-permeable chelator N, N,N ', N'-Tetrakis ( 2-pyridylmethyl ) ethylenediamine augmented
TLR4 mediated production of IFN-ß and subsequent synthesis of
inducible NO synthase and production of NO