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</svg>
PMID: 17275324
LBP is thought to be
a shuttle protein catalyzing LPS transfer from the outer membrane
of Gram-negative bacteria to CD14, another LPS binding
molecule.
PMID: 17275324
LBP is thought to be
a shuttle protein catalyzing LPS transfer from the outer membrane
of Gram-negative bacteria to CD14, another LPS binding
molecule.
indirect
PMID: 17275324
CD14 has
a role in loading LPS to the receptor complex consisting of TLR4
and MD-2.
PMID: 17275324,11150311
Recombinant EDA, but not other
recombinant fibronectin domains, induces expression of a matrix
methalloproteinase MMP-9 in human macrophages by stimulating
TLR4
PMID: 17275324
LPS is similar to a cytokine in that it interacts with a
receptor TLR4/MD-2, and induces oligomerization of TLR4,
leading to activation of downstream signaling pathways by
recruiting downstream adaptor molecules
PMID: 17275324,15557191,15010525,11521076
Direct interaction
between LPS and purified MD-2 without TLR4 was also
reported whereas the direct interaction between TLR4
and LPS has not been demonstrated.
PMID: 17275324
Figure 1
PMID: 17275324
‘MyD88-dependent’ pathway, requires two adaptor molecules,
myeloid differentiation factor 88 (MyD88) and MyD88 adapterlike
(Mal)/TIR domain-containing protein (TIRAP), and leads
to early activation of the transcription factor NF-KappaB, the production
of proinflammatory cytokines, and Th1 responses.
indirect
PMID: 17275324
Figure 1
PMID: 17275324
‘MyD88-dependent’ pathway, requires two adaptor molecules,
myeloid differentiation factor 88 (MyD88) and MyD88 adapterlike
(Mal)/TIR domain-containing protein (TIRAP), and leads
to early activation of the transcription factor NF-KappaB, the production
of proinflammatory cytokines, and Th1 responses.
indirect
indirect
PMID: 17275324
Figure 1
PMID: 17275324
‘MyD88-dependent’ pathway, requires two adaptor molecules,
myeloid differentiation factor 88 (MyD88) and MyD88 adapterlike
(Mal)/TIR domain-containing protein (TIRAP), and leads
to early activation of the transcription factor NF-kappaB, the production
of proinflammatory cytokines, and Th1 responses.
PMID: 17275324
Figure 1
PMID: 17275324
A second set of adaptor molecules, TIR domain-containing
adapter inducing interferon-beta (TRIF)/TIR domain-containing
adapter molecule-1 (TICAM-1) and TRIF-related adapter
molecule (TRAM)/TIR domain-containing adapter molecule-
2 (TICAM-2), are required for LPS-induced phosphorylation
and dimerization of the transcription factor IRF-3, leading to
interferon-beta (IFN-beta) production
indirect
PMID: 17275324
A second set of adaptor molecules, TIR domain-containing
adapter inducing interferon-beta (TRIF)/TIR domain-containing
adapter molecule-1 (TICAM-1) and TRIF-related adapter
molecule (TRAM)/TIR domain-containing adapter molecule-
2 (TICAM-2), are required for LPS-induced phosphorylation
and dimerization of the transcription factor IRF-3, leading to
interferon-beta (IFN-beta) production
indirect
PMID: 17275324
A second set of adaptor molecules, TIR domain-containing
adapter inducing interferon-beta (TRIF)/TIR domain-containing
adapter molecule-1 (TICAM-1) and TRIF-related adapter
molecule (TRAM)/TIR domain-containing adapter molecule-
2 (TICAM-2), are required for LPS-induced phosphorylation
and dimerization of the transcription factor IRF-3, leading to
interferon-beta (IFN-beta) production
PMID: 17275324
Figure 1
indirect
indirect
PMID: 17275324
A second set of adaptor molecules, TIR domain-containing
adapter inducing interferon-beta (TRIF)/TIR domain-containing
adapter molecule-1 (TICAM-1) and TRIF-related adapter
molecule (TRAM)/TIR domain-containing adapter molecule-
2 (TICAM-2), are required for LPS-induced phosphorylation
and dimerization of the transcription factor IRF-3, leading to
interferon-beta (IFN-beta) production
PMID: 17275324
Figure 1
PMID: 17275324
Tricacylated lipopeptide is
recognized by TLR1/TLR2, whereas diacylated lipopeptide is
sensed by TLR2/TLR6.
PMID: 17275324,15895089,15690042
CD14 is required for diacylated lipopeptides and
lipoteichoic acid whereas forward genetics revealed thatCD36 is another accessory molecule for TLR2 in its response
to diacylated lipopeptide and lipoteichoic acid
PMID: 17275324,15895089,15690042
CD14 is required for diacylated lipopeptides and
lipoteichoic acid whereas forward genetics revealed thatCD36 is another accessory molecule for TLR2 in its response
to diacylated lipopeptide and lipoteichoic acid
PMID: 17275324,15895089,15690042
CD14 is required for diacylated lipopeptides and
lipoteichoic acid whereas forward genetics revealed thatCD36 is another accessory molecule for TLR2 in its response
to diacylated lipopeptide and lipoteichoic acid
PMID: 17275324,15895089,15690042
CD14 is required for diacylated lipopeptides and
lipoteichoic acid whereas forward genetics revealed thatCD36 is another accessory molecule for TLR2 in its response
to diacylated lipopeptide and lipoteichoic acid
PMID: 17275324,15895089,15690042
CD14 is required for diacylated lipopeptides and
lipoteichoic acid whereas forward genetics revealed thatCD36 is another accessory molecule for TLR2 in its response
to diacylated lipopeptide and lipoteichoic acid
PMID: 17275324,15895089,15690042
CD14 is required for diacylated lipopeptides and
lipoteichoic acid whereas forward genetics revealed thatCD36 is another accessory molecule for TLR2 in its response
to diacylated lipopeptide and lipoteichoic acid
PMID: 17275324
A/D-type CpG is retained
for long periods in the endosomal vesicles of plasmacytoid dendritic
cells, together with the complex consisting of downstream
signaling molecules, whereas the B/K-type CpG. is recognized
by TLR9 in the lysosome.
PMID: 17275324
A/D-type CpG is retained
for long periods in the endosomal vesicles of plasmacytoid dendritic
cells, together with the complex consisting of downstream
signaling molecules, whereas the B/K-type CpG. is recognized
by TLR9 in the lysosome.
indirect
PMID: 17275324
The LPS coreceptor MD-2 was also shown to
facilitate glycosylation and cell surface expression of TLR4.
PMID: 17275324,7897216
Radioprotective 105 (RP105) is most similar to TLR4 in
extracellular leucine-rich repeats than other members of the Toll
family, and forms a complex with MD-1, cloning of which led to
the cloning of MD-2 as a molecule similar to MD-1
PMID: 17275324,15852007
A molecular mechanism by which
RP105/MD-1 contribute to B cell responses to TLR4/MD-2 and
TLR2 ligands was suggested by a recent report demonstrating
that RP105/MD-1 is associated with TLR4/MD-2
indirect
indirect
indirect
PMID: 17275324,10623794,11402040
HSP60-dependent induction of
TNF-alpha and NO in macrophages was dependent on TLR4 signaling
indirect
indirect
indirect
PMID: 17275324,10623794,11402040
HSP60-dependent induction of
TNF-alpha and NO in macrophages was dependent on TLR4 signaling
indirect
PMID: 17275324,11842086
HSP70 induces interleukin-12 (IL-12) production
in macrophages
indirect
indirect
PMID: 17275324,11912201
An ER chaperone gp96 induces production of proinflammatory
cytokines and upregulation of co-stimulatory
molecules in bone marrow DCs from wild type mice, whereas
DCs from TLR4 mutant or TLR4/TLR2 double mutant
mice failed to respond to gp96
indirect
PMID: 17275324,11912201
An ER chaperone gp96 induces production of proinflammatory
cytokines and upregulation of co-stimulatory
molecules in bone marrow DCs from wild type mice, whereas
DCs from TLR4 mutant or TLR4/TLR2 double mutant
mice failed to respond to gp96
PMID: 17275324
An ER chaperon gp96 is
associated with TLR4 in ER and required for cell surface expression
of TLR4
indirect
indirect
PMID: 17275324
An ER chaperon gp96 is
associated with TLR4 in ER and required for cell surface expression
of TLR4
PMID: 17275324
Biglycan, a small leucine-rich proteoglycan in ECM component,
acts on macrophages as an endogenous ligand of TLR4 and
TLR2, leading to rapid activation of p38, ERK, and NF-KappaB and
thereby stimulating the expression of TNF-alpha and macrophage
inflammatory protein-2 (MIP-2).
PMID: 17275324
Biglycan, a small leucine-rich proteoglycan in ECM component,
acts on macrophages as an endogenous ligand of TLR4 and
TLR2, leading to rapid activation of p38, ERK, and NF-KappaB and
thereby stimulating the expression of TNF-alpha and macrophage
inflammatory protein-2 (MIP-2).
indirect
PMID: 17275324
Biglycan, a small leucine-rich proteoglycan in ECM component,
acts on macrophages as an endogenous ligand of TLR4 and
TLR2, leading to rapid activation of p38, ERK, and NF-KappaB and
thereby stimulating the expression of TNF-alpha and macrophage
inflammatory protein-2 (MIP-2).
indirect
PMID: 17275324
Biglycan, a small leucine-rich proteoglycan in ECM component,
acts on macrophages as an endogenous ligand of TLR4 and
TLR2, leading to rapid activation of p38, ERK, and NF-KappaB and
thereby stimulating the expression of TNF-alpha and macrophage
inflammatory protein-2 (MIP-2).
indirect
PMID: 17275324
Biglycan, a small leucine-rich proteoglycan in ECM component,
acts on macrophages as an endogenous ligand of TLR4 and
TLR2, leading to rapid activation of p38, ERK, and NF-KappaB and
thereby stimulating the expression of TNF-alpha and macrophage
inflammatory protein-2 (MIP-2).
indirect
PMID: 17275324
Biglycan, a small leucine-rich proteoglycan in ECM component,
acts on macrophages as an endogenous ligand of TLR4 and
TLR2, leading to rapid activation of p38, ERK, and NF-KappaB and
thereby stimulating the expression of TNF-alpha and macrophage
inflammatory protein-2 (MIP-2).
indirect
PMID: 17275324
Biglycan, a small leucine-rich proteoglycan in ECM component,
acts on macrophages as an endogenous ligand of TLR4 and
TLR2, leading to rapid activation of p38, ERK, and NF-KappaB and
thereby stimulating the expression of TNF-alpha and macrophage
inflammatory protein-2 (MIP-2).
indirect
PMID: 17275324
Biglycan, a small leucine-rich proteoglycan in ECM component,
acts on macrophages as an endogenous ligand of TLR4 and
TLR2, leading to rapid activation of p38, ERK, and NF-KappaB and
thereby stimulating the expression of TNF-alpha and macrophage
inflammatory protein-2 (MIP-2).
indirect
indirect
indirect
indirect
indirect
indirect
PMID: 17275324
Moreover, biglycan was shown to be physically
associated with CD14/TLR4/MD-2.
indirect
PMID: 17275324,11150311
Recombinant EDA, but not other
recombinant fibronectin domains, induces expression of a matrix
methalloproteinase MMP-9 in human macrophages by stimulating
TLR4
PMID: 17275324
CD14 has
a role in loading LPS to the receptor complex consisting of TLR4
and MD-2.
PMID: 17275324,12055204
SP-A induces NF-KappaB activation and cytokine production such
as TNF-alpha and IL-10 in macrophages by stimulating TLR4
indirect
PMID: 17275324,12055204
SP-A induces NF-KappaB activation and cytokine production such
as TNF-alpha and IL-10 in macrophages by stimulating TLR4
indirect
indirect
PMID: 17275324,12055204
SP-A induces NF-KappaB activation and cytokine production such
as TNF-alpha and IL-10 in macrophages by stimulating TLR4
indirect
indirect
PMID: 17275324,12055204
SP-A induces NF-KappaB activation and cytokine production such
as TNF-alpha and IL-10 in macrophages by stimulating TLR4
PMID: 17275324,15795240
High-mobility group box 1 (HMGB1) was identified as an
endogenous ligand for TLR4/MD-2 and TLR2 that serves as a
late mediator of lethality in sepsis and as an early mediator of
inflammation and organ damage in hepatic ischemia reperfusion
injury, a pathophysiologic process whereby hypoxic organ damage
is accentuated following return of blood flow and oxygen
delivery
PMID: 17275324,15795240
High-mobility group box 1 (HMGB1) was identified as an
endogenous ligand for TLR4/MD-2 and TLR2 that serves as a
late mediator of lethality in sepsis and as an early mediator of
inflammation and organ damage in hepatic ischemia reperfusion
injury, a pathophysiologic process whereby hypoxic organ damage
is accentuated following return of blood flow and oxygen
delivery
indirect
indirect
PMID: 17275324
Oxidized low-density lipoprotein (OxLDL) induces actin
polymerization and spreading of macrophages, which results in
pro-atherogenic consequences as inhibition of phagocytosis of
apoptotic cells but enhancement of OxLDL uptake.
PMID: 17275324,12424240
This effect
is mediated by TLR4/MD-2 but not by TLR2
PMID: 17275324,12411706
Beta-Defensins are small antimicrobial peptides of the innate
immune system produced in response to microbial infection of
mucosal tissue and skin. Murine beta-defensin 2 (mDF2beta) acts
directly on immature dendritic cells as an endogenous ligand for
TLR4, inducing upregulation of co-stimulatory molecules and
dendritic cell maturation
indirect
PMID: 17275324,12411706
Beta-Defensins are small antimicrobial peptides of the innate
immune system produced in response to microbial infection of
mucosal tissue and skin. Murine beta-defensin 2 (mDF2beta) acts
directly on immature dendritic cells as an endogenous ligand for
TLR4, inducing upregulation of co-stimulatory molecules and
dendritic cell maturation