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Lipopolysaccharide (LPS), which binds to TLR4, is
one of the most well-studied PAMPs.

PMID: 18161744
TLR4 requires
MD-2 to recognize the active moiety of LPS.

PMID: 18161744
MD-2
is expressed as a dimer with TLR4 on the surface
of immune cells.







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Lipid A and its two derivatives,
monophosphoryl lipid A and lipid IVa, bind directly to
MD-2.</csml:comment>
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Lipid A engagement
results in activation of both MyD88-dependent
and TRIF-dependent (MyD88-independent) signalling
events, whereas monophosphoryl lipid A causes
primarily activation of TRIF-mediated signalling pathways.

PMID: 18161744,17569868 
Binding of Lipid IVa to MD-2–TLR4 complex
inhibits signalling events mediated by MyD88
and TRIF

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Lipid A engagement
results in activation of both MyD88-dependent
and TRIF-dependent (MyD88-independent) signalling
events, whereas monophosphoryl lipid A causes
primarily activation of TRIF-mediated signalling pathways.

</csml:comment>
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Lipid A and its two derivatives,
monophosphoryl lipid A and lipid IVa, bind directly to
MD-2.</csml:comment>
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Lipid A engagement
results in activation of both MyD88-dependent
and TRIF-dependent (MyD88-independent) signalling
events, whereas monophosphoryl lipid A causes
primarily activation of TRIF-mediated signalling pathways.

</csml:comment>
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<csml:comment type="text">PMID: 18161744
Lipid A and its two derivatives,
monophosphoryl lipid A and lipid IVa, bind directly to
MD-2.</csml:comment>
</csml:comments>
</csml:process>
<csml:process id="p8" name="p8" type="cso30:c:ProcessBiological">
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<csml:comments>
<csml:comment type="text">PMID: 18161744
NOD1 is encoded
by the caspase-recruitment domain 4 (CARD4) gene,
whereas NOD2 is encoded by the caspase-recruitment
domain 15 (CARD15) gene.</csml:comment>
</csml:comments>
</csml:process>
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<csml:comments>
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<csml:comments>
<csml:comment type="text">PMID: 18161744
NOD1 is encoded
by the caspase-recruitment domain 4 (CARD4) gene,
whereas NOD2 is encoded by the caspase-recruitment
domain 15 (CARD15) gene.</csml:comment>
</csml:comments>
</csml:process>
<csml:process id="p10" name="p8" type="cso30:c:ProcessBiological">
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<csml:processKinetic calcStyle="csml-calcStyle:speed" fast="false" kineticStyle="csml-kineticStyle:mass">
<csml:parameter key="coefficient2" value="1.0"/>
<csml:parameter key="coefficient1" value="0.1"/>
</csml:processKinetic>
</csml:processSimulationProperty>
<csml:viewProperty viewID="">
<csml:position position="auto" positionID="default" x="822.0" y="1422.0"/>
<csml:shape shapeID="default" visible="true">
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<csml:toolSpecificGraphics/>
</csml:shape>
</csml:viewProperty>
<csml:biologicalProperty refBiologicalEventID="cso30:i:ME_GeneExpression" refCellComponentID="cso30:i:CC_Nucleoplasm"/>
<csml:comments>
<csml:comment type="text">PMID: 18161744
NOD1 is encoded
by the caspase-recruitment domain 4 (CARD4) gene,
whereas NOD2 is encoded by the caspase-recruitment
domain 15 (CARD15) gene.</csml:comment>
</csml:comments>
</csml:process>
<csml:process id="p11" name="p9" type="cso30:c:ProcessBiological">
<csml:connector id="c31" name="c31" refID="G011270" type="cso30:c:InputAssociation">
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<csml:connectorKinetic>
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<csml:comments>
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</csml:processKinetic>
</csml:processSimulationProperty>
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<csml:position position="auto" positionID="default" x="988.0" y="1028.0"/>
<csml:shape shapeID="default" visible="true">
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<csml:toolSpecificGraphics/>
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<csml:biologicalProperty refBiologicalEventID="cso30:i:ME_Translation" refCellComponentID="cso30:i:CC_Cytosol"/>
<csml:comments>
<csml:comment type="text">PMID: 18161744
NOD1 is encoded
by the caspase-recruitment domain 4 (CARD4) gene,
whereas NOD2 is encoded by the caspase-recruitment
domain 15 (CARD15) gene.</csml:comment>
</csml:comments>
</csml:process>
<csml:process id="p12" name="p12" type="cso30:c:ProcessBiological">
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</csml:connector>
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Thus, NOD2
functions as a general sensor of most, if not all, bacteria,
whereas NOD1 senses primarily products yielded
from Gram-positive bacteria.</csml:comment>
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Thus, NOD2
functions as a general sensor of most, if not all, bacteria,
whereas NOD1 senses primarily products yielded
from Gram-positive bacteria.</csml:comment>
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Upon oligomerization of NOD1 or NOD2, the
recruitment of the serine/threonine kinase receptorinteracting
serine/threonine kinase (RICK; also known
as RIP2 or CARDIAK) occurs through a homophilic
CARD–CARD interaction.</csml:comment>
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<csml:comment type="text">PMID: 18161744
Upon oligomerization of NOD1 or NOD2, the
recruitment of the serine/threonine kinase receptorinteracting
serine/threonine kinase (RICK; also known
as RIP2 or CARDIAK) occurs through a homophilic
CARD–CARD interaction.</csml:comment>
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Upon oligomerization of NOD1 or NOD2, the
recruitment of the serine/threonine kinase receptorinteracting
serine/threonine kinase (RICK; also known
as RIP2 or CARDIAK) occurs through a homophilic
CARD–CARD interaction.
</csml:comment>
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Upon oligomerization of NOD1 or NOD2, the
recruitment of the serine/threonine kinase receptorinteracting
serine/threonine kinase (RICK; also known
as RIP2 or CARDIAK) occurs through a homophilic
CARD–CARD interaction.
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Instead, upon activation by NOD2, RICK induces
K63-linked polyubiquitylation of IKKgamma /NEMO at a
unique ubiquitylation site (Lysine-285)</csml:comment>
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It has
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associated with activation of the NF-KappaB pathway
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The interaction of RICK and IKKgamma /NEMO
leads to translocation of NF-KappaB transcription factors
to the nucleus.</csml:comment>
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</csml:processKinetic>
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<csml:comments>
<csml:comment type="text">PMID: 18161744,15692051 
In
addition to RICK, gene associated with retinoid-IFNinduced
mortality 19 (GRIM19) is another intracellular
molecule that has been associated with optimal NF-KappaB
activation induced by NOD2 but not NOD1</csml:comment>
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<csml:comments>
<csml:comment type="text"></csml:comment>
</csml:comments>
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<csml:priority value="0"/>
<csml:firing firingOnce="false" firingStyle="csml-firingStyle:and" type="csml-variable:Boolean" value="true"/>
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<csml:processKinetic calcStyle="csml-calcStyle:speed" fast="false" kineticStyle="csml-kineticStyle:mass">
<csml:parameter key="coefficient2" value="1.0"/>
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</csml:processKinetic>
</csml:processSimulationProperty>
<csml:viewProperty viewID="">
<csml:position position="auto" positionID="default" x="1310.0" y="566.0"/>
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<csml:biologicalProperty refBiologicalEventID="cso30:i:ME_Binding" refCellComponentID="cso30:i:CC_Cytosol"/>
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<csml:comment type="text">PMID: 18161744
For
example, PGN is a ligand for cell surface TLR2,
but upon uptake by macrophages, PGN can be processed
to yield MDP, a ligand for cytosolic NOD2.</csml:comment>
</csml:comments>
</csml:process>
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<csml:comments>
<csml:comment type="text"></csml:comment>
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</csml:processKinetic>
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<csml:comments>
<csml:comment type="text">PMID: 18161744,17038590,17038589
RIG-1, but not MDA5, can recognize uncapped 5prime2;-
triphosphate RNA (termed 3pRNA) present in viruses
that can only be generated by viral polymerases, while
MDA5 is the principle cytoplasmic receptor for synthetic
poly(I : C)</csml:comment>
</csml:comments>
</csml:process>
<csml:process id="p24" name="p23" type="cso30:c:ProcessBiological">
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<csml:comments>
<csml:comment type="text"></csml:comment>
</csml:comments>
</csml:connector>
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<csml:comments>
<csml:comment type="text"></csml:comment>
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<csml:comments>
<csml:comment type="text">PMID: 18161744,17038590,17038589
RIG-1, but not MDA5, can recognize uncapped 5prime2;-
triphosphate RNA (termed 3pRNA) present in viruses
that can only be generated by viral polymerases, while
MDA5 is the principle cytoplasmic receptor for synthetic
poly(I : C)</csml:comment>
</csml:comments>
</csml:process>
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<csml:comments>
<csml:comment type="text">indirect</csml:comment>
</csml:comments>
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<csml:comments>
<csml:comment type="text"></csml:comment>
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</csml:connector>
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Viral RNAs also activate
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2-5A activates RNase L to
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2-5A activates RNase L to
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2-5A activates RNase L to
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2-5A activates RNase L to
cleavage cellular RNAs to yield small self-RNA molecules, which are also recognized by RIG-I and/or MDA5.</csml:comment>
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The adaptor protein for RIG-1 and MDA5 is
named MAVS (VISA, CARDIF or IPS-1)

PMID: 18161744
MAVS is recruited and bound to RIG-1
or MDA5 via CARD–CARD interactions.</csml:comment>
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The adaptor protein for RIG-1 and MDA5 is
named MAVS (VISA, CARDIF or IPS-1)

PMID: 18161744
MAVS is recruited and bound to RIG-1
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Figure 1</csml:comment>
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Figure 1</csml:comment>
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Figure 1
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These events relay the signal through activation and translocation of NF-KappaB p65–p50 heterodimer and IRF3 as well
as IRF7 into the nucleus to activate downstream genes that encode alpha- and beta-interferon.</csml:comment>
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<csml:comment type="text">PMID: 18161744
These events relay the signal through activation and translocation of NF-KappaB p65–p50 heterodimer and IRF3 as well
as IRF7 into the nucleus to activate downstream genes that encode alpha- and beta-interferon.</csml:comment>
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TRAF3
has been shown to interact with MAVS, and be essential
for MAVS-mediated IFNalpha production and antiviral
responses.</csml:comment>
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<csml:comment type="text">PMID: 18161744
TRAF3
has been shown to interact with MAVS, and be essential
for MAVS-mediated IFNalpha production and antiviral
responses.</csml:comment>
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<csml:comment type="text">PMID: 18161744
Figure 1
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<csml:comment type="text">PMID: 18161744
Figure 1
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<csml:comment type="text">PMID: 18161744
Figure 1
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<csml:comment type="text">PMID: 18161744
Figure 1
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<csml:comment type="text">PMID: 18161744
Figure 1
</csml:comment>
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<csml:comment type="text">PMID: 18161744
Figure 1
</csml:comment>
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<csml:comment type="text">PMID: 18161744
Figure 1
</csml:comment>
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<csml:comment type="text">PMID: 18161744
Figure 1
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<csml:comment type="text">PMID: 18161744
These events relay the signal through activation and translocation of NF-KappaB p65–p50 heterodimer and IRF3 as well
as IRF7 into the nucleus to activate downstream genes that encode alpha- and beta-interferon.</csml:comment>
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<csml:comment type="text">PMID: 18161744
These events relay the signal through activation and translocation of NF-KappaB p65–p50 heterodimer and IRF3 as well
as IRF7 into the nucleus to activate downstream genes that encode alpha- and beta-interferon.</csml:comment>
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<csml:comment type="text">PMID: 18161744
These events relay the signal through activation and translocation of NF-KappaB p65–p50 heterodimer and IRF3 as well
as IRF7 into the nucleus to activate downstream genes that encode alpha- and beta-interferon.</csml:comment>
</csml:comments>
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These events relay the signal through activation and translocation of NF-KappaB p65–p50 heterodimer and IRF3 as well
as IRF7 into the nucleus to activate downstream genes that encode alpha- and beta-interferon.</csml:comment>
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These events relay the signal through activation and translocation of NF-KappaB p65–p50 heterodimer and IRF3 as well
as IRF7 into the nucleus to activate downstream genes that encode alpha- and beta-interferon.</csml:comment>
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These events relay the signal through activation and translocation of NF-KappaB p65–p50 heterodimer and IRF3 as well
as IRF7 into the nucleus to activate downstream genes that encode alpha- and beta-interferon.</csml:comment>
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In
macrophages, HSP60 induces the production of NO
and TNFalpha via TLR4</csml:comment>
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</csml:connector>
<csml:connector id="c158" name="c158" refID="MO000000289" type="cso30:c:OutputProcess">
<csml:connectorSimulationProperty>
<csml:connectorFiring connectorFiringStyle="csml-connectorFiringStyle:threshold" value="0"/>
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<csml:parameter key="stoichiometry" value="1"/>
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<csml:processKinetic calcStyle="csml-calcStyle:speed" fast="false" kineticStyle="csml-kineticStyle:mass">
<csml:parameter key="coefficient2" value="1.0"/>
<csml:parameter key="coefficient1" value="0.1"/>
</csml:processKinetic>
</csml:processSimulationProperty>
<csml:viewProperty viewID="">
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In
macrophages, HSP60 induces the production of NO
and TNFalpha via TLR4

PMID: 18161744,17321471,16339566
 Treatment
of macrophages with an agonist of the adenosine
A2A receptor (A2AR) inhibits TNF production, whereas agonists of A2BR increase IL-10 production
by a post-translational mechanism
</csml:comment>
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<csml:connectorFiring connectorFiringStyle="csml-connectorFiringStyle:threshold" value="0"/>
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<csml:comments>
<csml:comment type="text"></csml:comment>
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</csml:connector>
<csml:connector id="c162" name="c162" refID="e83" type="cso30:c:OutputProcess">
<csml:connectorSimulationProperty>
<csml:connectorFiring connectorFiringStyle="csml-connectorFiringStyle:threshold" value="0"/>
<csml:connectorKinetic>
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</csml:connectorSimulationProperty>
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</csml:viewProperty>
<csml:comments>
<csml:comment type="text"></csml:comment>
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</csml:connector>
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<csml:priority value="0"/>
<csml:firing firingOnce="false" firingStyle="csml-firingStyle:and" type="csml-variable:Boolean" value="true"/>
<csml:delay delayStyle="nodelay" value="0.0"/>
<csml:processKinetic calcStyle="csml-calcStyle:speed" fast="false" kineticStyle="csml-kineticStyle:mass">
<csml:parameter key="coefficient2" value="1.0"/>
<csml:parameter key="coefficient1" value="0.1"/>
</csml:processKinetic>
</csml:processSimulationProperty>
<csml:viewProperty viewID="">
<csml:position position="auto" positionID="default" x="1017.0" y="429.0"/>
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<csml:biologicalProperty refBiologicalEventID="cso30:i:ME_Binding" refCellComponentID="cso30:i:CC_Cytosol"/>
<csml:comments>
<csml:comment type="text">PMID: 18161744,11842086
TLR4 is also critical for
HSP70 induction of IL-12 production</csml:comment>
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</csml:process>
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<csml:connectorSimulationProperty>
<csml:connectorFiring connectorFiringStyle="csml-connectorFiringStyle:threshold" value="0"/>
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<csml:comments>
<csml:comment type="text"></csml:comment>
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</csml:connector>
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<csml:comments>
<csml:comment type="text"></csml:comment>
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<csml:comments>
<csml:comment type="text">PMID: 18161744,11912201
Gp96-
induced production of pro-inflammatory cytokines
and other co-stimulation factors from bone marrowderived
DCs is also dependent on TLR4 but it may
also involve TLR2</csml:comment>
</csml:comments>
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<csml:comments>
<csml:comment type="text"></csml:comment>
</csml:comments>
</csml:connector>
<csml:connector id="c170" name="c170" refID="e32" type="cso30:c:InputProcess">
<csml:connectorSimulationProperty>
<csml:connectorFiring connectorFiringStyle="csml-connectorFiringStyle:threshold" value="0"/>
<csml:connectorKinetic>
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</csml:connector>
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DCs is also dependent on TLR4 but it may
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Gp96-
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DCs is also dependent on TLR4 but it may
also involve TLR2

PMID: 18161744,12401407
These monocytes express high levels
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suppresses the production of pro-inflammatory
cytokines and removes damaged cells</csml:comment>
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Gp96-
induced production of pro-inflammatory cytokines
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DCs is also dependent on TLR4 but it may
also involve TLR2

PMID: 18161744,12401407
These monocytes express high levels
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suppresses the production of pro-inflammatory
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Gp96-
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DCs is also dependent on TLR4 but it may
also involve TLR2</csml:comment>
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Gp96-
induced production of pro-inflammatory cytokines
and other co-stimulation factors from bone marrowderived
DCs is also dependent on TLR4 but it may
also involve TLR2</csml:comment>
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<csml:comment type="text"></csml:comment>
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<csml:processKinetic calcStyle="csml-calcStyle:speed" fast="false" kineticStyle="csml-kineticStyle:mass">
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</csml:processKinetic>
</csml:processSimulationProperty>
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<csml:comment type="text">PMID: 18161744
CD44 is the major
cell surface receptor for hyaluronan, but recent evidence
indicates that hyaluronan can also bind to
and signal through TLR2 and TLR4.</csml:comment>
</csml:comments>
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<csml:comment type="text">PMID: 18161744
CD44 is the major
cell surface receptor for hyaluronan, but recent evidence
indicates that hyaluronan can also bind to
and signal through TLR2 and TLR4.</csml:comment>
</csml:comments>
</csml:process>
<csml:process id="p70" name="p68" type="cso30:c:ProcessBiological">
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<csml:comments>
<csml:comment type="text"></csml:comment>
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</csml:connector>
<csml:connector id="c191" name="c191" refID="MO000038320" type="cso30:c:InputProcess">
<csml:connectorSimulationProperty>
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<csml:connectorKinetic>
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</csml:connectorSimulationProperty>
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<csml:comment type="text">PMID: 18161744
CD44 is the major
cell surface receptor for hyaluronan, but recent evidence
indicates that hyaluronan can also bind to
and signal through TLR2 and TLR4.</csml:comment>
</csml:comments>
</csml:process>
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<csml:comments>
<csml:comment type="text"></csml:comment>
</csml:comments>
</csml:connector>
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<csml:connectorSimulationProperty>
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<csml:connectorKinetic>
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</csml:connectorKinetic>
</csml:connectorSimulationProperty>
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</csml:viewProperty>
<csml:comments>
<csml:comment type="text"></csml:comment>
</csml:comments>
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<csml:processSimulationProperty>
<csml:priority value="0"/>
<csml:firing firingOnce="false" firingStyle="csml-firingStyle:and" type="csml-variable:Boolean" value="true"/>
<csml:delay delayStyle="nodelay" value="0.0"/>
<csml:processKinetic calcStyle="csml-calcStyle:speed" fast="false" kineticStyle="csml-kineticStyle:mass">
<csml:parameter key="coefficient2" value="1.0"/>
<csml:parameter key="coefficient1" value="0.1"/>
</csml:processKinetic>
</csml:processSimulationProperty>
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<csml:shape shapeID="default" visible="true">
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<csml:toolSpecificGraphics/>
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<csml:biologicalProperty refBiologicalEventID="cso30:i:ME_Cleavage" refCellComponentID="cso30:i:CC_Extracellular"/>
<csml:comments>
<csml:comment type="text">PMID: 18161744
During tissue injury and/or
inflammation, however, hyaluronan is progressively
cleaved by a series of enzymatic reactions that yield
hyaluronic acids of smaller sizes.</csml:comment>
</csml:comments>
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<csml:comments>
<csml:comment type="text">indirect</csml:comment>
</csml:comments>
</csml:connector>
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<csml:connectorSimulationProperty>
<csml:connectorFiring connectorFiringStyle="csml-connectorFiringStyle:threshold" value="0"/>
<csml:connectorKinetic>
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<csml:comments>
<csml:comment type="text">indirect</csml:comment>
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Biglycan acts on macrophages to
produce TNFalpha and MIP-2 in a TLR2- and TLR4-
dependent manner

PMID: 18161744,17321471,16339566
 Treatment
of macrophages with an agonist of the adenosine
A2A receptor (A2AR) inhibits TNF production, whereas agonists of A2BR increase IL-10 production
by a post-translational mechanism
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Biglycan acts on macrophages to
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dependent manner

PMID: 18161744,17321471,16339566
 Treatment
of macrophages with an agonist of the adenosine
A2A receptor (A2AR) inhibits TNF production, whereas agonists of A2BR increase IL-10 production
by a post-translational mechanism
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<csml:comments>
<csml:comment type="text">PMID: 18161744
These proteins bind to the minor groove
of DNA with little sequence specificity and regulate
many transcriptional events, primarily by increasing
the binding affinity of transcription factors to their
corresponding DNA binding sites via bending or
distortion of the double helix.</csml:comment>
</csml:comments>
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<csml:comment type="text">PMID: 18161744,16267105
In fact FNEDA,
as an endogenous ligand for TLR4, has been
investigated as a potential adjuvant</csml:comment>
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Beta-Defensins interact with
CCR6 on the cell surface of both dendritic and T cells
to bridge innate and adaptive immunity</csml:comment>
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For example, human Beta-defensin 2
expression is dependent on NOD1, whereas Beta-defensin
3 expression is NOD1-independent but dependent on
EGFR and the ERK pathway</csml:comment>
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For example, human Beta-defensin 2
expression is dependent on NOD1, whereas Beta-defensin
3 expression is NOD1-independent but dependent on
EGFR and the ERK pathway</csml:comment>
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For example, human Beta-defensin 2
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3 expression is NOD1-independent but dependent on
EGFR and the ERK pathway</csml:comment>
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<csml:comments>
<csml:comment type="text">PMID: 18161744,16473764
The receptors for Ox-LDL are
in the scavenger receptor family, and include CD36
and a newly described family member termed lectinlike
oxidized lipoprotein scavenger receptor (LOX-
1)</csml:comment>
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Hyaluronan fragments isolated
from individuals with acute lung injuries can activate
macrophages to produce chemokines in a TLR2- and
TLR4-dependent fashion</csml:comment>
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Hyaluronan fragments isolated
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macrophages to produce chemokines in a TLR2- and
TLR4-dependent fashion</csml:comment>
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HMGB1 may either signal through multiple receptors
or associate with multiple ligands to signal through
different receptors. TLR4, TLR2 and TLR9 have
all been reported to respond to HMGB1</csml:comment>
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HMGB1 may either signal through multiple receptors
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all been reported to respond to HMGB1</csml:comment>
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HMGB1 may either signal through multiple receptors
or associate with multiple ligands to signal through
different receptors. TLR4, TLR2 and TLR9 have
all been reported to respond to HMGB1</csml:comment>
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The immunoglobulin ‘superfamily’ member RAGE has
also been reported to be a receptor for HMGB1</csml:comment>
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Recently, Coyle and colleagues showed that class A
CpG-containing oligodeoxynucleotides (ODNs) and
HMGB1 can form a complex.</csml:comment>
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The resultant complex
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plasmacytoid DCs to produce IFNalpha</csml:comment>
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<csml:comment type="text">PMID: 18161744
Recombinant
Fn-EDA, but not other domains of fibronectin,
was demonstrated to induce MMP-9 expression from
human macrophages via TLR4.</csml:comment>
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Fn-
EDA also activates NF-KappaB in macrophages.</csml:comment>
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The receptors for Ox-LDL are
in the scavenger receptor family, and include CD36
and a newly described family member termed lectinlike
oxidized lipoprotein scavenger receptor (LOX-
1)</csml:comment>
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Extracellular ATP appears to be required
for LPS-induced production of IL-1beta and IL-18 from
macrophages.</csml:comment>
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<csml:comment type="text">PMID: 18161744
Extracellular ATP appears to be required
for LPS-induced production of IL-1beta and IL-18 from
macrophages.</csml:comment>
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dying cells</csml:comment>
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In addition to ATP, other
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and Listeria monocytogenes, and RNA released from
dying cells</csml:comment>
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In addition to ATP, other
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and Listeria monocytogenes, and RNA released from
dying cells</csml:comment>
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In addition to ATP, other
molecules have the potential to interact with NALP3,
including nigericin, maitotoxin, Staphylococcus aureus
and Listeria monocytogenes, and RNA released from
dying cells</csml:comment>
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Upon interaction with its ligands,
NALP3 recruits ASC via PYD–PYD interactions, and
CARDINAL via NACHT–FIIND interactions, respectively.</csml:comment>
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By interaction with ASC, NALP3 triggers the
activation of caspase-1 and subsequent release of the
proinflammatory cytokines IL-1beta and IL-18.</csml:comment>
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By interaction with ASC, NALP3 triggers the
activation of caspase-1 and subsequent release of the
proinflammatory cytokines IL-1beta and IL-18
</csml:comment>
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By interaction with ASC, NALP3 triggers the
activation of caspase-1 and subsequent release of the
proinflammatory cytokines IL-1beta and IL-18
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Recently,
Vogl et al demonstrated a pivotal role of these proteins
in enhancing LPS-induced phagocyte activation
via their interaction with TLR4 in models of LPSinduced
shock and Escherichia coli-induced abdominal
sepsis</csml:comment>
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Recently,
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via their interaction with TLR4 in models of LPSinduced
shock and Escherichia coli-induced abdominal
sepsis</csml:comment>
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Mrp8 specifically interacts with the
TLR4–MD2 complex to induce intracellular translocation
of MyD88 and activation of IRAK-1 and NF-κB,
leading to transcriptional up-regulation of TNF gene
expression.</csml:comment>
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Mrp8 specifically interacts with the
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of MyD88 and activation of IRAK-1 and NF-κB,
leading to transcriptional up-regulation of TNF gene
expression.
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Mrp8 specifically interacts with the
TLR4–MD2 complex to induce intracellular translocation
of MyD88 and activation of IRAK-1 and NF-κB,
leading to transcriptional up-regulation of TNF gene
expression.
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Mrp8 specifically interacts with the
TLR4–MD2 complex to induce intracellular translocation
of MyD88 and activation of IRAK-1 and NF-κB,
leading to transcriptional up-regulation of TNF gene
expression.
</csml:comment>
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IL-10 not only
subverts the development of classical macrophage activation
responses but also stimulates macrophages to
express B7-H4, a novel member of the B7 family of T
cell co-stimulator molecules</csml:comment>
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RegIIIgamma can bind to a carbohydrate component
of PGN to kill the bacteria.</csml:comment>
</csml:comments>
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<csml:comment type="text">PMID: 18161744
The metabolism of the C20 fatty acid eicosapentaenoic
acid by COX2 can result in the formation of so-called resolvins, which were named because
of their ability to contribute to the resolution of
inflammation.</csml:comment>
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It can also be generated
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 Treatment
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 Treatment
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by a post-translational mechanism
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 Treatment
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by a post-translational mechanism
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 Treatment
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by a post-translational mechanism
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 Treatment
of macrophages with an agonist of the adenosine
A2A receptor (A2AR) inhibits TNF production, whereas agonists of A2BR increase IL-10 production
by a post-translational mechanism
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Furthermore,
the co-stimulation of macrophages with agonists of
TLRs and A2AR results in an increase in VEGF
production by macrophages</csml:comment>
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Furthermore,
the co-stimulation of macrophages with agonists of
TLRs and A2AR results in an increase in VEGF
production by macrophages</csml:comment>
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<csml:comment type="text">PMID: 18161744,12401407
These monocytes express high levels
of formyl-peptide receptor 1 (FPR1), which, when ligated,
suppresses the production of pro-inflammatory
cytokines and removes damaged cells</csml:comment>
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<csml:comments>
<csml:comment type="text"></csml:comment>
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