◀ Back to MED1
MED1 — MED4
Pathways - manually collected, often from reviews:
-
Reactome Reaction:
MED4
→
MED1
(reaction)
Rachez et al., Nature 1999, Näär et al., Annu Rev Biochem 2001, Bourbon et al., Mol Cell 2004, Malik et al., Trends Biochem Sci 2005, Maston et al., Annu Rev Genomics Hum Genet 2006, Kelleher et al., Cell 1990, Rachez et al., Genes Dev 1998, Yuan et al., Proc Natl Acad Sci U S A 1998
-
Reactome Reaction:
MED4
→
MED1
(direct_complex)
Rachez et al., Nature 1999, Näär et al., Annu Rev Biochem 2001, Bourbon et al., Mol Cell 2004, Malik et al., Trends Biochem Sci 2005, Maston et al., Annu Rev Genomics Hum Genet 2006, Kelleher et al., Cell 1990, Rachez et al., Genes Dev 1998, Yuan et al., Proc Natl Acad Sci U S A 1998
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
-
IRef Bind Interaction:
Complex of 55 proteins
Sato et al., Mol Cell 2004
-
IRef Bind Interaction:
Complex of 35 proteins
Sato et al., Mol Cell 2004
-
IRef Bind Interaction:
Complex of 58 proteins
Sato et al., Mol Cell 2004
-
IRef Bind Interaction:
Complex of 71 proteins
Sato et al., Mol Cell 2004
-
IRef Bind Interaction:
Complex of 101 proteins
Sato et al., Mol Cell 2004
-
IRef Bind Interaction:
Complex of 62 proteins
Sato et al., Mol Cell 2004
-
IRef Biogrid Interaction:
MED1
—
MED4
(colocalization, biochemical)
Havugimana et al., Cell 2012
-
IRef Biogrid Interaction:
MED1
—
MED4
(physical association, affinity chromatography technology)
Zhang et al., Mol Cell 2005
-
IRef Biogrid Interaction:
MED1
—
MED4
(physical association, affinity chromatography technology)
Malovannaya et al., Proc Natl Acad Sci U S A 2010
-
MIPS CORUM Mediator complex:
Mediator complex complex (CCNC-CDK19-CDK8-MED1-MED10-MED11-MED12-MED13-MED13L-MED14-MED15-MED16-MED17-MED18-MED20-MED21-MED22-MED23-MED24-MED25-MED26-MED27-MED28-MED29-MED30-MED31-MED4-MED6-MED7-MED8-MED9-MED19)
Sato et al., Mol Cell 2004
-
MIPS CORUM ARC complex:
ARC complex complex (ACAD8-MED1-MED12-MED13-MED14-MED15-MED17-MED23-MED24-MED25-MED26-MED4-MED6-MED7-MED8)
Näär et al., Nature 1999
-
MIPS CORUM TRAP complex:
TRAP complex complex (CCNC-MED1-MED10-MED12-MED13-MED14-MED16-MED17-MED21-MED24-MED27-MED31-MED4-MED6-THRA-THRAP3)
Ito et al., Mol Cell 1999
-
MIPS CORUM Mediator complex:
Mediator complex complex (MED1-MED10-MED11-MED13-MED13L-MED14-MED15-MED16-MED17-MED18-MED20-MED21-MED22-MED23-MED24-MED25-MED26-MED27-MED29-MED30-MED31-MED4-MED6-MED7-MED8-MED19-OPA1)
Sato et al., J Biol Chem 2003
-
MIPS CORUM SMCC complex:
SMCC complex complex (CCNC-CDK8-MED1-MED12-MED13-MED14-MED16-MED17-MED21-MED24-MED27-MED4-MED6-THRAP3)
Ito et al., Mol Cell 1999
-
MIPS CORUM DRIP complex:
DRIP complex complex (MED1-MED12-MED13-MED14-MED16-MED17-MED23-MED24-MED26-MED4-MED6-MED7-RXRB-VDR)
Rachez et al., Genes Dev 1998
-
MIPS CORUM DRIP complex:
DRIP complex complex (MED1-MED12-MED13-MED14-MED16-MED17-MED23-MED24-MED26-MED4-MED6-MED7-RXRB-VDR)
Rachez et al., Nature 1999
-
MIPS CORUM TRAP-SMCC mediator complex:
TRAP-SMCC mediator complex complex (MED1-MED11-MED17-MED18-MED22-MED25-MED29-MED4-MED8-MED19)
Tomomori-Sato et al., J Biol Chem 2004
-
IRef Corum Interaction:
Complex of 16 proteins
(association, affinity chromatography technology)
Näär et al., Nature 1999
-
IRef Corum Interaction:
Complex of 15 proteins
(association, affinity chromatography technology)
Ito et al., Mol Cell 1999
-
IRef Corum Interaction:
Complex of 65 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., Mol Cell 2004
-
IRef Corum Interaction:
Complex of 21 proteins
(association, cosedimentation through density gradient)
Tomomori-Sato et al., J Biol Chem 2004
-
IRef Corum Interaction:
Complex of 43 proteins
(association, affinity chromatography technology)
Rachez et al., Nature 1999
-
IRef Corum Interaction:
Complex of 17 proteins
(association, affinity chromatography technology)
Ito et al., Mol Cell 1999
-
IRef Corum Interaction:
Complex of 28 proteins
(association, affinity chromatography technology)
Sato et al., J Biol Chem 2003
-
Gene Ontology Complexes mediator complex:
mediator complex complex (MED29-MED28-MED20-MED23-MED22-MED27-MED1-MED6-MED7-MED4-MED8-MED9-PPARGC1B-MED10-MED11-MED12-MED13-MED14-MED15-MED17-MED18-MED19-THRAP3-MED30-MED31-MED13L)
Ito et al., Mol Cell 1999, Kressler et al., J Biol Chem 2002, Ge et al., Nature 2002, Tomomori-Sato et al., J Biol Chem 2004, Lee et al., EMBO J 2007, Lee et al., Mol Cell Biol 1997, Xiao et al., J Biol Chem 1999
-
IRef Intact Interaction:
Complex of 12 proteins
(association, anti tag coimmunoprecipitation)
Tomomori-Sato et al., J Biol Chem 2004
-
IRef Intact Interaction:
Complex of 43 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., Mol Cell 2004
-
IRef Intact Interaction:
Complex of 27 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., J Biol Chem 2003
-
IRef Intact Interaction:
Complex of 115 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., Mol Cell 2004
-
IRef Intact Interaction:
Complex of 30 proteins
(association, anti tag coimmunoprecipitation)
Tomomori-Sato et al., J Biol Chem 2004
-
IRef Intact Interaction:
Complex of 82 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., Mol Cell 2004
-
IRef Intact Interaction:
Complex of 26 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., J Biol Chem 2003
-
IRef Intact Interaction:
Complex of 64 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., Mol Cell 2004
-
IRef Intact Interaction:
Complex of 34 proteins
(association, tandem affinity purification)
Varjosalo et al., Cell reports 2013
-
IRef Intact Interaction:
Complex of 31 proteins
(association, tandem affinity purification)
Varjosalo et al., Cell reports 2013
-
IRef Intact Interaction:
Complex of 64 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., Mol Cell 2004
-
IRef Intact Interaction:
Complex of MED18-MED17-MED1-POLR2A-MED4-MED26-MED8-MED6
(association, anti tag coimmunoprecipitation)
Takahashi et al., Cell 2011
-
IRef Intact Interaction:
Complex of 12 proteins
(association, anti tag coimmunoprecipitation)
Tomomori-Sato et al., J Biol Chem 2004
-
IRef Intact Interaction:
Complex of MED29-MED11-MED1-MED19-MED17-MED19-MED8-MED22-MED4
(association, anti tag coimmunoprecipitation)
Tomomori-Sato et al., J Biol Chem 2004
-
IRef Intact Interaction:
Complex of 143 proteins
(association, cosedimentation through density gradient)
Nassa et al., Proteomics 2011
-
IRef Intact Interaction:
Complex of 26 proteins
(physical association, ion exchange chromatography)
Sato et al., Mol Cell 2004
-
IRef Intact Interaction:
Complex of 68 proteins
(association, anti tag coimmunoprecipitation)
Sato et al., Mol Cell 2004
-
IRef Intact Interaction:
Complex of 31 proteins
(physical association, ion exchange chromatography)
Sato et al., Mol Cell 2004
-
IRef Intact Interaction:
Complex of 11 proteins
(association, anti tag coimmunoprecipitation)
Tomomori-Sato et al., J Biol Chem 2004
Text-mined interactions from Literome
Lee et al., Mol Cell Biol 1999
:
The
Mediator complex of Saccharomyces cerevisiae is
required for both general and regulated transcription of
RNA polymerase II (PolII) and is composed of two stable subcomplexes ( Srb4 and Rgr1 subcomplexes )
Strukova et al., Biochemistry (Mosc) 1999
(Inflammation) :
TRAP-6 inhibited
PAF release from A23187 activated RPMC via an NO-dependent mechanism
Ekhterae et al., Circ Res 1999
:
Loss of endogenous ARC in the cytosol of H9c2 cells was associated with translocation of
ARC from the cytosol to intracellular membranes, release of cytochrome c from the mitochondria,
activation of
caspase-3 , poly ( ADP-ribose ) polymerase ( PARP ) cleavage, and DNA fragmentation
Hoshi et al., J Biol Chem 2000
:
NF-kappaB was activated after the stimulation of TRAP, bFGF, and TNF-alpha in electrophoretic mobility shift assay, and E5510 suppressed the NF-kappaB activation
induced by
TRAP and bFGF but not the activation by
TNF-alpha ... NF-kappaB was activated after the stimulation of TRAP, bFGF, and TNF-alpha in electrophoretic mobility shift assay, and E5510 suppressed the
NF-kappaB activation
induced by
TRAP and bFGF but not the activation by TNF-alpha ... The phosphorylation of
ERK1/2 was rapidly
induced by
TRAP and bFGF but not by TNF-alpha ... These results indicate that
TRAP and bFGF
induced I-kappaB degradation and
NF-kappaB activation through a distinct pathway from TNF-alpha and that ERK1/2 may play an important role in NF-kappaB activation induced by TRAP and bFGF
Spåhr et al., J Biol Chem 2000
:
This stimulation was species-specific, because S. pombe
Mediator could not
stimulate TFIIH purified from S. cerevisiae
Ohmori et al., Biochemistry 2000
:
While BAPTA-AM ( an intracellular Ca2+ chelator ) inhibited
Cas phosphorylation
induced by collagen or
TRAP , Ro31-8220 ( a PKC inhibitor ) rather prolonged it
Guzowski et al., J Neurosci 2001
:
Arc RNA expression differed from that of zif268 and c-fos in two regards : ( 1 ) hippocampal
Arc RNA levels were correlated with learning of the hippocampal dependent spatial, but not hippocampal independent cued response, water task, and ( 2 )
Arc RNA levels in the hippocampus and entorhinal cortex
increased after spatial reversal learning relative to an asymptotic performance group
Kimura et al., Planta Med 2001
:
Intercellular adhesion molecule-1 ( ICAM-1 ) expression was also
induced by thrombin, but not by
TRAP
Waltereit et al., J Neurosci 2001
:
Arg3.1/Arc mRNA
induction by
Ca2+ and cAMP requires protein kinase A and mitogen activated protein kinase/extracellular regulated kinase activation ...
Arg3.1/Arc mRNA induction by Ca2+ and cAMP
requires protein kinase A and
mitogen activated protein kinase/extracellular regulated kinase activation
Weber et al., Blood 2001
:
ADP induced fibrinogen binding was completely inhibited by 10 microg/mL abciximab, 30 nM tirofiban, or 3 microg/mL eptifibatide, while
fibrinogen binding
induced by 100 microM
TRAP was inhibited only by 50 %
de Rossi et al., Anesth Analg 2001
:
In contrast, halothane reduced
TRAP-6 induced activation of the
GPIIb/IIIa complex
Mittler et al., EMBO Rep 2001
:
Novel critical
role of a human
Mediator complex for basal
RNA polymerase II transcription
Huang et al., Zhonghua Xue Ye Xue Za Zhi 1999
:
The expression of GPIb was reduced while the expressions of
GPIIb/IIIa , IIIa, P-selectin increased after the platelets were
activated by
TRAP
Sakai et al., J Biochem 2001
:
Receptor activator of
NF-kappaB ( RANKL ) significantly
increased the LBC levels of cathepsin K,
TRAP , and c-Src, whereas calcitonin decreased the LBC levels of cathepsin K, TRAP, and Rab7, indicating that the transformation of early to late endosomal elements and lysosomes in OCLs is also regulated by osteoclastogenesis regulatory factors
Elmquist et al., Physiol Behav 2001
(Body Weight) :
We found that
leptin activates neurons in the retrochiasmatic area ( RCA ) and lateral
arcuate nucleus (Arc) that innervate the sympathetic preganglionic neurons in the thoracic spinal cord and also contain cocaine- and amphetamine regulated transcript ( CART )
Kremerskothen et al., Neurosci Lett 2002
(Neuroblastoma) :
Insulin induced expression of the activity regulated cytoskeleton associated gene (
ARC ) in human neuroblastoma cells
requires p21(ras) , mitogen activated protein kinase/extracellular regulated kinase and src tyrosine kinases but is protein kinase C-independent ...
Insulin induced expression of the activity regulated cytoskeleton associated gene (
ARC ) in human neuroblastoma cells requires p21(ras), mitogen activated protein kinase/extracellular regulated kinase and src tyrosine kinases but is protein kinase C-independent
Ying et al., J Neurosci 2002
:
Brain derived neurotrophic factor induces long-term potentiation in intact adult hippocampus :
requirement for ERK activation coupled to CREB and upregulation of
Arc synthesis
Espinola et al., Thromb Haemost 2002
:
TRAP increased the expression of
GPIIb/IIIa and GPIIIa on platelet surface ...
TRAP increased the expression of GPIIb/IIIa and
GPIIIa on platelet surface
Wang et al., J Biol Chem 2002
:
Mediator role of platelet derived growth factor and
ERK
Delerive et al., Mol Endocrinol 2002
:
By contrast,
DRIP205 is not
involved in PPARalpha mediated
NF-kappaB transcriptional repression
Wang et al., J Virol 2002
(Cell Transformation, Viral) :
Much of the large E1A bound to Mediator in 293 cells is in a stable complex that includes RNA polymerase II, leading us to suggest that the interaction of E1A-CR3 with
Mediator stabilizes the interaction of
Mediator with the polymerase
Shui et al., Calcif Tissue Int 2002
:
The combination of rapamycin ( 10 ng/ml ) and TGF-beta1 ( 1 ng/ml ) increased
TRAP+MNC 3.1- and 6.9-fold as compared with rapamycin or TGF-beta1 alone, respectively, and enhanced CTR mRNA expression
induced by
TGF-beta1 by 1.9-fold
Wang et al., J Biol Chem 2002
(Prostatic Neoplasms) :
A coregulatory
role for the
TRAP-mediator complex in
androgen receptor mediated gene expression
Sheu et al., J Biol Chem 2003
:
Moreover, we show that TRAP interacts with TRIP intracellularly, that activation of the
TGFbeta type II receptor by TRIP-1 occurs in the
presence of
TRAP and that the differentiation process is mediated through the Smad2/3 pathway ... Moreover, we show that TRAP interacts with TRIP intracellularly, that activation of the TGFbeta type II receptor by
TRIP-1 occurs in the
presence of
TRAP and that the differentiation process is mediated through the Smad2/3 pathway
Proulx et al., Endocrinology 2002
(Weight Gain) :
In the
arcuate nucleus (ARC) , acute
leptin increased SOCS-3 and POMC mRNA levels, but decreased NPY mRNA levels in the rostral part of ARC
Acevedo et al., Mol Cell Biol 2003
:
We have used a biochemical approach, including an in vitro chromatin assembly and transcription system, to examine the functional
role for
Mediator in the transcriptional activity of
estrogen receptor alpha (ERalpha) with chromatin templates, as well as functional interplay between Mediator and p300/CBP during ERalpha dependent transcription ... Using three different approaches to functionally inactivate Mediator ( immunoneutralization, immunodepletion, and inhibitory polypeptides ), we find that
Mediator is
required for maximal transcriptional activation by ligand activated
ERalpha
Billheimer et al., Thromb Res 2002
(Thrombosis) :
All four fibans inhibited ADP and
TRAP stimulated
fibrinogen binding and microaggregate formation in a concentration dependent manner, whereas P-selectin expression was relatively unaltered
Liu et al., J Biol Chem 2003
:
Moreover, the binding is significantly enhanced in EMSA with nuclear extracts from RANKL treated RAW264.7 cells and BMMs, suggesting that the 12-bp sequence may be involved in
RANKL induced
TRAP transcription ... Importantly, mutation of the USF binding site partially blocks
RANKL induced
TRAP transcription in RAW264.7 cells, confirming that USF1 and USF2 are functionally involved in RANKL induced TRAP transcription ... Importantly, mutation of the USF binding site partially blocks RANKL induced TRAP transcription in RAW264.7 cells, confirming that
USF1 and USF2 are functionally
involved in RANKL induced
TRAP transcription ... Importantly, mutation of the USF binding site partially blocks RANKL induced TRAP transcription in RAW264.7 cells, confirming that USF1 and
USF2 are functionally
involved in RANKL induced
TRAP transcription
Kumpawat et al., Mutat Res 2003
(Chromosome Aberrations) :
The present data indicate that the generation of ROS by ARC could partially contribute to the induction of chromosomal aberrations (CAs), since the frequency of
ARC induced
CAs was reduced either by post-treatment with superoxide dismutase ( SOD ) or in anoxic conditions
Zakharova et al., J Biol Chem 2003
:
Furthermore, in a system with purified proteins and naked DNA,
STAT1alpha- and STAT1beta dependent transcription is
stimulated by the
TRAP/Mediator co-activator complex ... Furthermore, in a system with purified proteins and naked DNA,
STAT1alpha- and STAT1beta dependent transcription is
stimulated by the
TRAP/Mediator co-activator complex ... Furthermore, in a system with purified proteins and naked DNA,
STAT1alpha- and STAT1beta dependent transcription is
stimulated by the
TRAP/Mediator co-activator complex ... Furthermore, in a system with purified proteins and naked DNA,
STAT1alpha- and STAT1beta dependent transcription is
stimulated by the
TRAP/Mediator co-activator complex
Reiter et al., Thromb Haemost 2003
(Endotoxemia...) :
PAR1 decreased by approximately 8 % ( p < 0.001 ) within 2 h after endotoxin infusion and stayed at those levels until 6 h. Concomitantly,
TRAP induced P-selectin expression maximally decreased by 18 % ( p < 0.001 ) at 6 h ... PAR1 decreased by approximately 8 % ( p < 0.001 ) within 2 h after endotoxin infusion and stayed at those levels until 6 h. Concomitantly,
TRAP induced
P-selectin expression maximally decreased by 18 % ( p < 0.001 ) at 6 h
Malabu et al., Peptides 1992
(Body Weight) :
We tested the hypothesis that low plasma
insulin levels
stimulate ARC levels of NPY in fasted rats
Fujimoto et al., J Neurosci Res 2004
(Seizures) :
Arc interacts with microtubules/microtubule associated protein 2 and
attenuates microtubule associated protein 2 immunoreactivity in the dendrites ... We found that the overexpression of
Arc as well as
Arc induction by seizure in vivo decreased microtubule associated protein 2 (MAP2) staining in the dendrites by immunocytochemistry, although MAP2 content was not changed on Western blot
Guidi et al., J Biol Chem 2004
:
Mediator , a global transcriptional co-activator, dramatically
enhances the phosphorylation of the
CTD of RNA pol II by holo-TFIIH in vitro ... Using purified proteins we have determined that the subunits of TFIIK are sufficient for Mediator to enhance Kin28 CTD kinase activity and that
Mediator enhances phosphorylation of a
glutathione S-transferase-CTD fusion protein, despite the absence of multiple Mediator and/or TFIIH interactions with polymerase ... Using purified proteins we have determined that the subunits of TFIIK are sufficient for Mediator to enhance Kin28 CTD kinase activity and that
Mediator enhances phosphorylation of a glutathione
S-transferase-CTD fusion protein, despite the absence of multiple Mediator and/or TFIIH interactions with polymerase
Sato et al., Mol Cell 2004
:
The
Mediator is a multiprotein transcriptional coactivator that is expressed ubiquitously in eukaryotes from yeast to mammals and is
required for induction of
RNA polymerase II (pol II) transcription by DNA binding transcription factors ... The
Mediator is a multiprotein transcriptional coactivator that is expressed ubiquitously in eukaryotes from yeast to mammals and is
required for induction of RNA
polymerase II (pol II) transcription by DNA binding transcription factors
Pineda Torra et al., J Biol Chem 2004
:
Requirement for the
FXR/RXR heterodimer in the
DRIP205-FXR interaction was evaluated using an RXR heterodimerization-deficient FXR mutant ( FXRL433R )
Wang et al., Genetics 2004
:
The rgr1 and sin4 constitutive phenotype does not require either the MAL-activator or maltose permease, indicating that
Mediator represses
MAL basal expression ... The
role of the
Mediator in
MAL gene regulation is discussed
Shi et al., Gene 2004
:
Functionally, mutation of the YY1 binding site resulted in a reduction in the RANKL induced TRAP transcription in RAW264.7 cells, demonstrating that YY1 positively regulates
RANKL induced
TRAP transcriptional activation ... Functionally, mutation of the YY1 binding site resulted in a reduction in the RANKL induced TRAP transcription in RAW264.7 cells, demonstrating that
YY1 positively
regulates RANKL induced
TRAP transcriptional activation
Hassan et al., Proc Natl Acad Sci U S A 1992
:
Regulatory
roles of Fnr, Fur, and
Arc in expression of manganese containing
superoxide dismutase in Escherichia coli
Fukushima et al., Bone 2005
:
The addition of cell-permeable PKI, an inhibitor of the cAMP/PKA signaling pathway, to the cocultures 8 h after the IL-1alpha stimulation inhibited
IL-1alpha induced
TRAP+ cell formation ... IL-1alpha induced
TRAP+ cell formation was completely
blocked by either NS398, a selective inhibitor of
cyclooxygenase (COX)-2 , or PD98059, a specific inhibitor of extracellular signal regulated kinase ( ERK ) ...
IL-1alpha induced
TRAP+ cell formation was completely blocked by either NS398, a selective inhibitor of cyclooxygenase (COX)-2, or PD98059, a specific inhibitor of extracellular signal regulated kinase ( ERK ) ... IL-1alpha induced
TRAP+ cell formation was completely
blocked by either NS398, a selective inhibitor of cyclooxygenase
(COX)-2 , or PD98059, a specific inhibitor of extracellular signal regulated kinase ( ERK )
Fukushima et al., J Dent Res 2005
:
The PKC inhibitor, Ro-32-0432, suppressed RANKL expression in PDL cells and
PTHrP induced
TRAP+ cell formation
Pavri et al., Mol Cell 2005
:
Importantly,
Mediator was inactive ( Cdk8+ ) under basal conditions but was
activated (
Cdk8- ) upon induction
Malik et al., Trends Biochem Sci 2005
:
Dynamic
regulation of
pol II transcription by the mammalian
Mediator complex
Smith et al., Endocrinology 2005
(Body Weight) :
In the
arcuate nucleus (Arc) ,
KiSS-1 expression
increased after ovariectomy and decreased with E2 treatment
Ljusberg et al., J Biol Chem 2005
:
Activation of
TRAP by
cathepsin K/L was because of increases in catalytic activity, substrate affinity, and sensitivity to reductants ...
Activation of
TRAP by
cathepsin K/L was because of increases in catalytic activity, substrate affinity, and sensitivity to reductants
Govind et al., Mol Cell Biol 2005
:
We confirm the
roles of
Mediator and SAGA in
TATA binding protein (TBP) recruitment and demonstrate that all four coactivators under study enhance Pol II recruitment or promoter clearance following TBP binding
Gaertner et al., J Control Release 2005
:
The mechanism by which
ARC-encapsulation increased
IFN-gamma activity in vivo remains uncertain
Bramham et al., Prog Neurobiol 2005
:
Recent experiments suggest that
BDNF activates synaptic consolidation through transcription and rapid dendritic trafficking of mRNA encoded by the immediate early gene,
Arc
Stephenson et al., The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2005
(Fetal Membranes, Premature Rupture) :
TRAP-14 , a thrombin receptor agonist, also significantly
increased MMP-9 levels, suggesting that thrombin induced changes in MMP-9 expression were mediated through the thrombin receptor
Soulet et al., Journal of thrombosis and haemostasis : JTH 2005
:
Conversely, secreted ADP strongly potentiated
Rac activation
induced by FcgammaRIIa clustering or
TRAP via its P2Y12 receptor, the target of antithrombotic thienopyridines
Takagi et al., J Biol Chem 2006
:
Taken together, these findings lead to the suggestion that
Mediator is
required for basal
RNA polymerase II transcription in vivo
Kim et al., J Biol Chem 2006
(Bone Resorption) :
We propose that the
MCP-1 induced
TRAP ( + ) /CTR ( + ) multinuclear cells represent an arrested stage in osteoclast differentiation, after NFATc1 induction and cellular fusion but prior to the development of bone resorption activity
Sarker et al., Pathophysiol Haemost Thromb 2005
(Calcium Signaling...) :
Previously, we showed that thrombin and the thrombin receptor agonist peptide (
TRAP-14 ; SFLLRNPNDKYEPF ) for protease activated receptor 1 (PAR1)
induce vascular endothelial growth factor ( VEGF ) secretion in PC-12 cells ... In this study, we show that thrombin and
TRAP-14 also
stimulate VEGF secretion in the human NB-1 neuroblastoma cells
Wang et al., Neurosci Lett 2006
:
Consistent with the literature,
Arc , an indicator of synaptic plasticity, was
induced by
BDNF ( 25 ng/ml ) in both dose- and time dependent manners
Schneider et al., Can J Appl Physiol 2005
:
In plasma,
LPO decreased from 3589 +/- 193 to 3274 +/- 223 cps x mg Hb ( -1 ) ( p < 0.05 ), and
TRAP increased from 304 +/- 45 to 384 +/- 57 micromol x L ( -1 ) trolox ( p < 0.05 ) after high intensity exercise in T. GPx activity increased in the T group as compared to the UT group, after exercise in moderate ( 25.90 +/- 3.79 to 15.05 +/- 3.23 nM x min ( -1 ) x mg protein ( -1 ) ) and high ( 21.75 +/- 4.91 to 12.1 +/- 2.46 nM x min ( -1 ) x mg protein ( -1 ) ) intensities ( p < 0.05 )
Radhakrishnan et al., Cancer Res 2006
(Neoplasms...) :
Specifically,
ARC inhibits the phosphorylation of
RNA polymerase II by positive transcription elongation factor-b, leading to a block in transcriptional elongation ... Although
ARC promoted the accumulation of
p53 , ARC induced apoptosis in tumor cells was p53 independent, suggesting that it may be useful for the treatment of tumors with functionally inactive p53
Kim et al., J Biol Chem 2006
:
The beta-catenin transactivation domain bound directly to isolated MED12 and intact Mediator both in vitro and in vivo, and
Mediator was recruited to Wnt-responsive genes in a
beta-catenin dependent manner
Steinberg et al., Endocrinology 2006
(Obesity) :
Intracerebroventricular
CNTF ( Ax15 ) reduced food intake,
increased arcuate nucleus (ARC) signal transducer and activator of transcription 3 phosphorylation, and reduced AMPK signaling but not in the paraventricular nucleus ( PVN ), posterior hypothalamus, or cortex ... Both leptin and
CNTF reduced AMPK activity and acetyl-coenzyme A carboxylase phosphorylation in the
ARC and PVN of control fed mice ... Both
leptin and CNTF
reduced AMPK activity and acetyl-coenzyme A carboxylase phosphorylation in the
ARC and PVN of control fed mice
Chen et al., Assay Drug Dev Technol 2006
:
Compound 1 did not affect the
tumor necrosis factor-alpha- or lipopolysaccharide induced
TRAP-luciferase response , suggesting selective inhibition of the RANKL induced pathway
Black et al., Mol Cell 2006
:
Using purified proteins, we found that the
Mediator regulates this assembly process by binding to p300 and
TFIID
Zhou et al., Mol Cell Biol 2006
:
We propose that activated Gli3 physically targets the MED12 interface within Mediator in order to functionally reverse
Mediator dependent suppression of
Shh target gene transcription
Duarte et al., Biochem Biophys Res Commun 2006
:
Similarly to thrombin,
FGF1 expression and release were
induced by
TRAP , a specific oligopeptide agonist of PAR1 ... Similarly to thrombin,
FGF1 expression and release were
induced by
TRAP , a specific oligopeptide agonist of PAR1
Tzingounis et al., Neuron 2006
:
These studies show that
Arc/Arg3.1 regulates
endophilin 3 and dynamin 2, two components of the endocytosis machinery ... These studies show that
Arc/Arg3.1 regulates endophilin 3 and
dynamin 2 , two components of the endocytosis machinery
Foo et al., J Biol Chem 2007
(Myocardial Reperfusion Injury) :
Here we show that degradation of
ARC is
dependent on the p53 induced ubiquitin E3 ligase,
MDM2 ... Furthermore,
ARC degradation
requires MDM2 , because MDM2 knock-out fibroblasts showed defective ARC degradation that could be rescued by MDM2
Gopalakrishnan et al., Biochem Cell Biol 2006
(Diabetes Mellitus, Experimental) :
In the vertebrae,
TRAP activity was elevated as a result of diabetes, but this was
prevented by
insulin or estradiol
Hunter et al., FEBS Lett 2007
:
ARC-overexpression inhibited myoblast differentiation associated
caspase-3 activation, suggesting ARC inhibits myogenic differentiation through caspase inhibition
Speziani et al., Eur J Immunol 2007
:
IL-2,
IFN-gamma and IL-4
inhibit TRAP and bone resorption activities contrary to IL-10, which enhances both activities ...
IL-2 , IFN-gamma and IL-4
inhibit TRAP and bone resorption activities contrary to IL-10, which enhances both activities ... IL-2, IFN-gamma and
IL-4 inhibit
TRAP and bone resorption activities contrary to IL-10, which enhances both activities
Meng et al., Anticancer Drugs 2007
(Anoxia) :
ARC-111 , a small-molecule
topoisomerase I inhibitor , is a potent cytotoxic drug against multiple human cancer cell lines under normoxic conditions ( Li et al., Cancer Res 2003 ; 63 : 8400-8407 )
Arriagada et al., J Steroid Biochem Mol Biol 2007
:
We find that both mutation of serine 208 to aspartic acid ( VDRS208D ) or phosphorylation of
VDR by CKII
enhance the interaction of VDR with
DRIP205 in the presence of 1alpha,25-dihydroxy Vitamin D3
Patel et al., Platelets 2007
:
Platelet reactivity was evaluated by measuring platelet aggregation, platelet leukocyte aggregates ( PLA ) formation in response to a 6-mer thrombin receptor agonist peptide (TRAP) at a final concentration of 40 microM and flow cytometry determined
P-selectin expression
induced by ADP,
TRAP and arachidonic acid ( AA )
de Foubert et al., Neuroscience 2007
:
The present study investigated the
effects of
5-HT(6)-receptor activation on hippocampal and cortical levels of mRNA expression of BDNF and
Arc in the rat
Boldt et al., Vox Sang 2007
:
B-HES but not NB-HES increases the expression of activated platelet
GP IIb/IIIa induced by ADP or
TRAP
Flaujac et al., Thromb Haemost 2007
(Postoperative Hemorrhage) :
Platelet activation marker expression (
CD62P and activated alphaIIbbeta3 )
induced by ADP or
TRAP was lower after CPB than before CPB, suggesting a deleterious effect of normothermic CPB on platelet function
Liu et al., Mol Cell Biol 2008
:
STAF65gamma is
required for SPT3/STAGA interaction with core
Mediator and for MYC recruitment of SPT3, TAF9, and core Mediator components to the TERT promoter but is dispensable for MYC recruitment of TRRAP, GCN5, and p300 and for acetylation of nucleosomes and loading of TFIID and RNA polymerase II on the promoter
Li et al., Aging Cell 2007
:
Aging up-regulated expression of Bax, Bcl2 and
ARC ,
down-regulated XIAP expression and did not affect p53, pp53 and Omi/HtrA2 ... Aging up-regulated expression of Bax, Bcl2 and
ARC , down-regulated XIAP expression and did not
affect p53 , pp53 and Omi/HtrA2 ... Aging up-regulated expression of Bax, Bcl2 and
ARC , down-regulated XIAP expression and did not
affect p53, pp53 and
Omi/HtrA2
Ge et al., Mol Cell Biol 2008
:
These results indicate that there is a conditional requirement for MED1/TRAP220 and that a direct interaction between PPARgamma and
Mediator through MED1/TRAP220 is not
essential either for PPARgamma stimulated adipogenesis or for
PPARgamma target gene expression in cultured fibroblasts ... As
Mediator is apparently
essential for
PPARgamma transcriptional activity, our data indicate the presence of alternative mechanisms for Mediator recruitment, possibly through intermediate cofactors or other cofactors that are functionally redundant with MED1/TRAP220
Leite et al., J Neuroendocrinol 2008
:
ERalpha expression in TH-ir neurones
increased at 14 and 16 h in the
rostral-ARC and dorsomedial-ARC, 14 h in the caudal-ARC and 16 h in the VMPO, whereas it was unaltered in the ventrolateral-ARC, periventricular and AVPe
Echeverria et al., Curr Alzheimer Res 2007
:
Using a model of synaptic plasticity in which
BDNF increases
Arc expression in cultured cortical neurons, we have found that an oligomeric form of Abeta strongly inhibits the BDNF induced increase of Arc expression
Ariyoshi et al., J Cell Biochem 2008
(Bone Resorption) :
Heparin suppressed TRAP positive multinucleated cell formation and
TRAP activity
induced by
RANKL , whereas the other GAGs showed no effects on osteoclast differentiation
Christersson et al., Journal of thrombosis and haemostasis : JTH 2008
:
TRAP and P-selectin
increased TF,
IL8 , and MCP-1 mRNA in whole blood and purified monocytes
Belakavadi et al., Mol Cell Biol 2008
:
Here, we report that phosphorylation of
MED1 by mitogen activated protein kinase-extracellular signal regulated kinase ( MAPK-ERK )
promotes its association with
Mediator
Mancino et al., Dig Liver Dis 2009
(Bile Duct Neoplasms...) :
17beta-Estradiol stimulated proliferation of HuH-28 cells was blocked by 70 % by
VEGF-TRAP , a receptor based
VEGF inhibitor
Contreras-Levicoy et al., FEBS J 2008
:
Activation of transcription by
PC4 was
dependent on the
Mediator complex and TFIIA, but was independent of TATA binding protein associated factor
Kauskot et al., Frontiers in bioscience : a journal and virtual library 2008
:
The disintegrin inhibited the binding of FITC-fibrinogen and
FITC-PAC-1 to ADP stimulated platelets and
inhibited ADP-,
TRAP- and collagen induced aggregation of murine, rabbit or human platelets ... The disintegrin inhibited the binding of
FITC-fibrinogen and FITC-PAC-1 to ADP stimulated platelets and
inhibited ADP-,
TRAP- and collagen induced aggregation of murine, rabbit or human platelets
Keifer et al., Neurobiol Learn Mem 2008
(Synaptic Transmission) :
The results are consistent with the interpretation that synaptic incorporation of GluR4 containing AMPARs supports the expression of
CRs in this preparation, and that
Arc may be
involved in trafficking of GluR4 subunits during conditioning
Karanasios et al., J Mol Biol 2008
:
Furthermore, the C-terminal part of Arc1p harbors a conserved tRNA binding domain ( TRBD ) required for the
Arc1p dependent stimulation of the catalytic activity of
MetRS
Tsutsui et al., Genes Cells 2008
:
While the role of CDK8 has been studied extensively, little is known of the
role of
CDK11 in
Mediator
Thiaville et al., Nucleic Acids Res 2008
:
It is unclear whether
Mediator complex in yeast is
necessary for all
RNA polymerase II (Pol II) transcription or if it is limited to genes activated by environmental stress
Zheng et al., J Neurosci Res 2009
:
In contrast, chelating intracellular calcium ( [ Ca ( 2+ ) ] ( i ) ) by BAPTA-AM abolished
BDNF mediated
Arc up-regulation ... Surprisingly, BAPTA-AM did not block ERK activation, indicating that [ Ca ( 2+ ) ] ( i ) and Ras-Raf-MAPK are not coupled, and the activation of
ERK alone is not
sufficient to up-regulate
Arc transcription ... Moreover, we found that inhibition of
calmodulin (CaM) by W13
blocked both
Arc transcription and ERK activation, revealing a Ca ( 2+ ) -independent function of CaM
Ambati et al., Biofactors 2007
(Body Weight) :
Leptin and
CNTF increased
ARC-ME mRNA levels of signal transducer and activator of transcription 3 ( STAT3 ) by 64.5 and 124.7 % ( p < 0.01 ), suppressor of cytokine signaling 3 ( SOCS3 ) by 258.9 and 1063.9 % ( p < 0.01 ), cocaine and amphetamine regulated transcript ( CART ) by 102.7 and 123.1 % ( p < 0.01 ), and proopiomelanocortin ( POMC2 ) by 374.1 and 264.9 % ( p < 0.01 ), respectively ...
Leptin and CNTF
increased ARC-ME mRNA levels of signal transducer and activator of transcription 3 ( STAT3 ) by 64.5 and 124.7 % ( p < 0.01 ), suppressor of cytokine signaling 3 ( SOCS3 ) by 258.9 and 1063.9 % ( p < 0.01 ), cocaine and amphetamine regulated transcript ( CART ) by 102.7 and 123.1 % ( p < 0.01 ), and proopiomelanocortin ( POMC2 ) by 374.1 and 264.9 % ( p < 0.01 ), respectively
Chauleur et al., Journal of thrombosis and haemostasis : JTH 2008
(Postpartum Hemorrhage) :
From values obtained 6-9 months after delivery, low ( but not-deficient ) levels of fibrinogen, von Willebrand factor (VWF) antigen, factor (F) XI, platelet CD42b,
TRAP induced increase of platelet
CD41a and high values of serum residual prothrombin activity or closure aperture times using the collagen-ADP cartridge on the PFA-100 system, and blood group O, were independently associated with a significant risk of severe PPH. Being positive for at least two of these eight variables was found in 1.6 %, 3.5 % and 20.8 % of the women from the C, the NS-PPH and the S-PPH groups, respectively, the odds ratio for S-PPH in such a case being 16.4, 95 % CI ( 6.5-41 ), P < 0.0001
Messerli et al., Phytother Res 2009
(Neoplasms, Experimental...) :
Artepillin C (ARC) in Brazilian green propolis selectively
blocks oncogenic
PAK1 signaling and suppresses the growth of NF tumors in mice ... Also it was demonstrated that ARC suppresses angiogenesis, suggesting the possibility that
ARC also
blocks oncogenic
PAK1 signaling ... Here it is shown for the first time that both
ARC and green propolis extract ( GPE ) indeed
block the
PAK1 signaling selectively, without affecting another kinase known as AKT
Bae et al., Thromb Haemost 2009
:
Furthermore, similar to activated protein C, both thrombin and
TRAP activated Rac1 and
inhibited the activation of
RhoA and NF-kappaB pathways in response to TNF-alpha in cells pretreated with protein C-S195A ... Furthermore, similar to activated protein C, both thrombin and
TRAP activated
Rac1 and inhibited the activation of RhoA and NF-kappaB pathways in response to TNF-alpha in cells pretreated with protein C-S195A
Chen et al., J Neurosci Res 2009
:
In this study,
BDNF treatment alone
induced the activation of the phosphatidylinositol 3-kinase-Akt-mammlian target of rapamycin ( PI3K-Akt-mTOR ) signaling pathway, the phosphorylation of eukaryotic initiation factor 4E binding protein ( 4EBP1 ) and p70 ribosomal S6 kinase (p70S6K), the dephosphorylation of eukaryotic elongation factor 2 ( eEF2 ), and the expression of
Arc
Simpson et al., Arq Bras Endocrinol Metabol 2009
(Obesity) :
Firmly established pathways
involve the orexigenic
NPY/AgRP and the anorexigenic POMC/CART neurons in the
arcuate nucleus (ARC) of the hypothalamus ... Firmly established pathways
involve the orexigenic
NPY/AgRP and the anorexigenic POMC/CART neurons in the
arcuate nucleus (ARC) of the hypothalamus
Chandler et al., Thromb Res 2010
(Coronary Disease) :
Platelet activation by adenosine diphosphate ( ADP ) or
thrombin agonist peptide (TRAP) increased
CD62P and CD40L surface density in the presence of aspirin by 1.9 - 2.8 -fold ... Platelet activation by adenosine diphosphate ( ADP ) or
thrombin agonist peptide (TRAP) increased CD62P and
CD40L surface density in the presence of aspirin by 1.9 - 2.8 -fold
Kirk et al., PloS one 2009
(Hyperphagia...) :
At postnatal Day 30, before the onset of hyperphagia in these animals, serum
leptin is normal, but leptin induced appetite suppression and phosphorylation of STAT3 in the
arcuate nucleus (ARC) are
attenuated ; the level of AgRP-immunoreactivity in the hypothalamic paraventricular nucleus ( PVH ), which derives from neurones in the ARC and is developmentally dependent on leptin, is also diminished
Villanueva et al., Endocrinology 2009
:
Furthermore, ghrelin, which activates orexigenic ARC neurons, increased
ARC mTORC1 activity and
induced colocalized pS6- and
c-Fos-IR
Kim et al., J Cell Physiol 2009
(Bone Resorption) :
We found that saurolactam was one of the compounds inhibiting the RANKL induced osteoclastogenesis ; it significantly inhibited the
RANKL induced
TRAP activity and formation of multinucleated osteoclasts without any cytotoxicity
Konda et al., Journal of inflammation (London, England) 2009
:
The inhibitory effect of RIAA on inflammatory markers was assessed by measuring nitric oxide in LPS stimulated RAW 264.7 cells,
RANKL mediated
TRAP activity in transformed osteoclasts, and TNF-alpha/IL-1beta mediated MMP-13 expression in SW1353 cells ... In addition, RIAA inhibited NF-kappaB mediated inflammatory markers in various cell models, including nitric oxide in LPS stimulated RAW 264.7 cells,
RANKL mediated
TRAP activity in transformed osteoclasts, and TNF-alpha/IL-1beta mediated MMP-13 expression in SW1353 human chondrosarcoma cells ... In addition, RIAA inhibited
NF-kappaB mediated inflammatory markers in various cell models, including nitric oxide in LPS stimulated RAW 264.7 cells, RANKL mediated
TRAP activity in transformed osteoclasts, and TNF-alpha/IL-1beta mediated MMP-13 expression in SW1353 human chondrosarcoma cells
Mazière et al., J Cell Physiol 2009
(Bone Resorption) :
Finally, OxLDL also prevented
RANKL induced
TRAP activity and RANKL induced bone resorbing activity of human peripheral blood mononuclear cells
Panja et al., J Biol Chem 2009
:
These results support a dominant
role for
ERK-MNK signaling in control of translational initiation and
Arc synthesis during LTP consolidation in the dentate gyrus ... These results support a dominant
role for
ERK-MNK signaling in control of translational initiation and
Arc synthesis during LTP consolidation in the dentate gyrus
Yu et al., J Biol Chem 2009
:
To determine whether
IL-4 regulates
TRAP promoter activity, RAW264.7 cells were transfected with a TRAP promoter-luciferase reporter ...
STAT6VT did not
inhibit the potent up-regulation of
TRAP promoter activity caused by overexpression of NFATc1, PU.1, and microphthalmia transcription factor, downstream targets of macrophage colony stimulating factor and RANKL ... Knockdown of NFATc1 by short interfering RNA caused TRAP expression to be down-regulated, and ectopic expression of NFATc1 abrogated the
IL-4 induced down-regulation of
TRAP ... These results suggest that
STAT6 plays two distinct roles in
TRAP expression ... However, in the absence of RANKL and osteoclast differentiation,
STAT6 binds the TRAP promoter after IL-4 treatment and directly
enhances TRAP expression ... However, in the absence of RANKL and osteoclast differentiation,
STAT6 binds the TRAP promoter after IL-4 treatment and directly
enhances TRAP expression
Frank et al., Brain Behav Immun 2010
(Escherichia coli Infections...) :
IL-1RA blocks E. coli
induced suppression of
Arc and long-term memory in aged F344xBN F1 rats
Schwartz et al., Endocrinology 1991
(Obesity) :
Thus,
insulin reduced the expression of mRNA for NPY specifically in the
ARC
Kim et al., J Cell Physiol 2010
(Colonic Neoplasms) :
Indeed,
ARC-G blocked expression of UPR target genes such as phosphorylated-PERK, ATF4,
CHOP , and GRP78, which was accompanied by enhanced phosphorylation of eIF2 alpha during glucose deprivation ... Indeed,
ARC-G blocked expression of UPR target genes such as phosphorylated-PERK, ATF4, CHOP, and
GRP78 , which was accompanied by enhanced phosphorylation of eIF2 alpha during glucose deprivation ... Indeed,
ARC-G blocked expression of UPR target genes such as phosphorylated-PERK,
ATF4 , CHOP, and GRP78, which was accompanied by enhanced phosphorylation of eIF2 alpha during glucose deprivation
Qi et al., Endocrinology 2010
:
It is widely accepted that
leptin acts on first-order neurons in the
arcuate nucleus (ARC) with information then relayed to other hypothalamic centers ... We used a model of hypothalamo-pituitary disconnection ( HPD ) to determine whether
leptin action on appetite regulating systems
requires the
ARC
Crespin et al., Blood Coagul Fibrinolysis 2009
:
Inhibition of Cdc42 and Rac1 by toxin B from Clostridium difficile, that suppresses
PAK1/2 activation
induced by
TRAP and collagen or by A23187 in the presence of calpeptin, decreases polymerization of actin, lamellipodia and filopodia formation and interferes with the shedding of microvesicles
Li et al., Apoptosis 2010
:
ARC ( apoptosis repressor with caspase recruitment domain ), an abundantly expressed apoptotic repressor in cardiomyocytes, could
inhibit mitochondrial fission and
Smac/DIABLO release
Carey et al., Cold Spring Harbor protocols 2010
:
INTRODUCTION : The
Mediator ( Med ) complex plays a key role in promoter-specific activation of transcription by
RNA polymerase II (Pol II)
Kunin et al., PloS one 2010
:
Mediator of DNA damage checkpoint 1 ( MDC1 )
contributes to high NaCl induced activation of the osmoprotective transcription factor
TonEBP/OREBP
Arzamendi et al., Clin Appl Thromb Hemost 2011
(Coronary Artery Disease...) :
In contrast to abciximab,
ARC1779 did not significantly
affect platelet aggregation,
P-selectin expression, and platelet-leukocyte binding
Xu et al., EMBO Rep 2011
(Alzheimer Disease) :
Mediator , in a
MED12 dependent manner, occupies only AICD bound promoter DNA, indicating that the AICD recruits Mediator to activate transcription
Harlan et al., Circ Res 2011
(Disease Models, Animal...) :
These data demonstrate a critical
role for
ObR in the
ARC in mediating the sympathetic nerve responses to leptin and in the adverse sympathoexcitatory effects of leptin in obesity
Alberi et al., Neuron 2011
:
Thus, Notch signaling is dynamically regulated in response to neuronal activity,
Arc/Arg3.1 is a context dependent Notch regulator, and
Notch1 is
required for the synaptic plasticity that contributes to memory formation
Quennell et al., Endocrinology 2011
(Body Weight...) :
In mice with normalized levels of estradiol,
leptin deficiency markedly
reduced kisspeptin gene expression, particularly in the
arcuate nucleus (ARC) , and kisspeptin immunoreactive cell numbers in the rostral periventricular region of the third ventricle ( RP3V )
Roth et al., Pediatr Res 2011
(Body Weight...) :
We compared the metabolic phenotype of animals with three distinct types of hypothalamic lesions : 1 ) destruction of the
arcuate nucleus (ARC) induced by monosodium glutamate ( MSG ), 2 ) electrolytic lesion of the adjacent ventromedial nucleus ( VMN ) alone, 3 ) both the VMN and
dorsomedial nucleus (DMN) , or a 4 ) combined medial hypothalamic lesion ( CMHL ) affecting the VMN, DMN, and the ARC
Franco et al., Exp Cell Res 2011
(Bone Resorption) :
Furthermore, MMP-9 enzyme inhibitor also attenuated both
RANKL induced osteoclastogenesis and up-regulation of
TRAP and cathepsin K mRNA expression, indicating that MMP-9 enzyme action is engaged in the promotion of RANKL induced osteoclastogenesis ... Furthermore,
MMP-9 enzyme inhibitor also
attenuated both RANKL induced osteoclastogenesis and up-regulation of
TRAP and cathepsin K mRNA expression, indicating that MMP-9 enzyme action is engaged in the promotion of RANKL induced osteoclastogenesis ... Finally, Dox treatment abrogated
RANKL induced osteoclastogenesis and
TRAP activity in mouse calvaria along with the suppression of MMP9 enzyme activity, again without affecting the expression of MMP9 protein
Zheng et al., Curr Eye Res 2011
(Cataract) :
Its downstream p53 was inhibited, and FOXO pathway was activated, indicating that
SIRT1 may
play a protective role in
ARC formation
Andino et al., J Endocrinol 2011
(Body Weight...) :
Interestingly, tyrosine hydroxylase levels were
increased in both the
ARC and VTA with
POMC overexpression in either the ARC or the VTA
Corbin et al., International journal of nephrology and renovascular disease 2011
:
Active renin mass concentration (ARC) is
independent of the endogenous level of
angiotensinogen , and less variable and more reproducible than plasma renin activity
Resch et al., Am J Physiol Regul Integr Comp Physiol 2011
:
One hour after PACAP administration, expression of pro-opiomelanocortin mRNA was significantly
increased in the
arcuate nuclei (ARC) , with no changes in
neuropeptide Y and agouti related polypeptide mRNA levels
Lin et al., Genes Dev 2011
:
Studies in depleted extracts showed that the
Mediator coactivator complex, which controls PIC assembly, is also
necessary for
CHD1 recruitment
Kumar et al., J Biol Chem 2012
(Synaptic Transmission) :
Mechanistically, intracellular mGluR5 mediated Arc induction is dependent upon extracellular and intracellular Ca ( 2+ ) and ERK1/2 as well as calmodulin dependent kinases as known chelators, inhibitors, and a dominant negative Ca ( 2+ )
/calmodulin dependent protein kinase II construct block
Arc increases ... Mechanistically, intracellular mGluR5 mediated
Arc induction is
dependent upon extracellular and intracellular Ca ( 2+ ) and
ERK1/2 as well as calmodulin dependent kinases as known chelators, inhibitors, and a dominant negative Ca ( 2+ ) /calmodulin dependent protein kinase II construct block Arc increases ... Mechanistically, intracellular
mGluR5 mediated
Arc induction is dependent upon extracellular and intracellular Ca ( 2+ ) and ERK1/2 as well as calmodulin dependent kinases as known chelators, inhibitors, and a dominant negative Ca ( 2+ ) /calmodulin dependent protein kinase II construct block Arc increases ... Moreover, intracellular mGluR5 induced
Arc expression
requires the serum response
transcription factor ( SRF ) as wild type but not SRF-deficient neurons show this response ... Moreover, intracellular
mGluR5 induced
Arc expression requires the serum response transcription factor ( SRF ) as wild type but not SRF-deficient neurons show this response
Yi et al., Diabetes 2012
(Insulin Resistance) :
Antagonizing the
NPY1 receptors by intracerebroventricular infusion of its antagonist largely
blocked the hepatic insulin resistance induced by dexamethasone in the
ARC
An et al., Hepatology 2012
(Disease Models, Animal...) :
Here, we investigated the in vivo
effects of
ARC fused with the transduction domain of human immunodeficiency virus 1 ( HIV-1 ) ( TAT-ARC ) on
Fas- and tumor necrosis factor (TNF) mediated murine models of fulminant liver failure
Ang et al., PLoS Biol 2012
:
Furthermore, we have found that
Mediator controls the galactose induced protein degradation of
Gal80 , which places Mediator genetically upstream of the activator Gal4 ... Furthermore, we have found that
Mediator controls the galactose induced protein degradation of Gal80, which places Mediator genetically upstream of the activator
Gal4
Holloway-Erickson et al., Frontiers in behavioral neuroscience 2012
:
Memory modulating BLA manipulations influence expression of the protein product of the immediate early gene activity regulated cytoskeletal associated protein (
Arc ) in the dorsal hippocampus, and hippocampal expression of
Arc protein is critically
involved in memory consolidation and long-term potentiation
Tai et al., Blood 2012
(Multiple Myeloma...) :
PCI-32765 blocked RANKL/M-CSF induced phosphorylation of
Btk and downstream PLC-?2 in OCs,
resulting in diminished
TRAP5b ( ED50 = 17 nM ) and bone resorption activity ... PCI-32765 blocked RANKL/M-CSF induced phosphorylation of Btk and downstream
PLC-?2 in OCs,
resulting in diminished
TRAP5b ( ED50 = 17 nM ) and bone resorption activity
Zhang et al., Biochimie 2012
(Bone Resorption) :
Besides,
RANKL induced osteoclast formation from RAW 264.7 cells and the expression of
TRAP , CA II, CTSK and MMP-9 was significantly reduced by the treatment of 25 µM HEF and 17ß-estradiol ( ES ), and the inhibitory strength increases in the order TF < ES < ICA < BS, which was blocked by ICI182780 suggesting that the regulation of osteoclast activity might be ER dependent
Chitu et al., Blood 2012
(Bone Diseases, Metabolic...) :
PSTPIP2 tyrosine phosphorylation and a functional F-BAR domain were essential for
PSTPIP2 inhibition of
TRAP expression and osteoclast precursor fusion, whereas interaction with PEST-type phosphatases was only required for suppression of TRAP expression
Riediger et al., Proc Nutr Soc 2012
(Obesity...) :
PYY and
leptin also reverse or
prevent fasting induced activation of the
ARC ...
PYY and leptin also reverse or
prevent fasting induced activation of the
ARC
Tong et al., J Neurosci 2012
:
Using rat organotypic hippocampal cultures, we found that
IL-1ß suppressed BDNF dependent regulation of
Arc and phosphorylation of cofilin and cAMP response element binding protein ( CREB ), a transcription factor regulating Arc expression ... Using rat organotypic hippocampal cultures, we found that IL-1ß suppressed
BDNF dependent regulation of
Arc and phosphorylation of cofilin and cAMP response element binding protein ( CREB ), a transcription factor regulating Arc expression ... Using rat organotypic hippocampal cultures, we found that IL-1ß suppressed BDNF dependent regulation of Arc and phosphorylation of cofilin and cAMP response element binding protein ( CREB ), a
transcription factor regulating
Arc expression
Povolny et al., Exp Hematol 1990
:
In addition, the effect of 1,25-dihydroxyvitamin D3 ( calcitriol ) on
CSF induced colony growth and
TRAP expression was also determined
Lewis et al., Clin Exp Allergy 2013
:
Mediator release
induced by
SCF was accompanied by the up-regulation of the activation marker, CD63
Tikhonova et al., Chin J Physiol 2012
:
BDNF also
augmented mRNA levels of
Arc gene encoding Arc ( Activity regulated cytoskeleton associated ) protein involved in BDNF induced processes of neuronal and synaptic plasticity in hippocampus and prefrontal cortex
Naidu et al., Chem Biol Interact 2013
(Arthritis, Experimental...) :
The peptide YR-11 ( YLEIEFSLKHR ), obtained by direct substitution of cysteine with a serine residue in the template sequence, significantly ( p < 0.05 ) inhibited RANK-RANKL binding, and
RANKL induced
TRAP activity and formation of multinucleated osteoclasts without any cytotoxicity
Gremmel et al., Translational research : the journal of laboratory and clinical medicine 2013
(Obesity...) :
Finally, PAR-1 mediated platelet activation as assessed by expression of
P-selectin and activated GPIIb/IIIa in
response to
TRAP-6 was significantly more pronounced in obese patients than in patients without obesity ( both P = 0.02 ) ... Finally, PAR-1 mediated platelet activation as assessed by expression of P-selectin and activated
GPIIb/IIIa in
response to
TRAP-6 was significantly more pronounced in obese patients than in patients without obesity ( both P = 0.02 )
Lu et al., J Biol Chem 2013
(Calcium Signaling...) :
Moreover, we showed that
Foxo3a activates
ARC expression by directly binding to its promoter
Kim et al., J Biol Chem 2013
:
Mediator recruitment to heat shock genes
requires dual Hsf1 activation domains and mediator tail subunits
Med15 and Med16 ...
Mediator recruitment to heat shock genes
requires dual Hsf1 activation domains and mediator tail subunits Med15 and
Med16
Verger et al., Nucleic Acids Res 2013
:
We further show that depletion of
MED25 disrupts the association of ERM with the
Mediator in vitro
Chen et al., Int J Biochem Cell Biol 2013
:
When stimulated with 12-O-tetradecanoylphorbol 13-acetate ( TPA ) or CD437, this
TR3-TRAP? interaction not only induced Ca ( 2+ ) depletion in the endoplasmic reticulum ( ER ) but also
promoted the expression of the proapoptotic transcriptional regulator
CHOP
Galbraith et al., Cell 2013
(Neoplasms) :
HIF1A Employs
CDK8-Mediator to
Stimulate RNAPII
Elongation in Response to Hypoxia ...
HIF1A induces binding of
CDK8-Mediator and the super elongation complex ( SEC ), containing AFF4 and CDK9, to alleviate RNAPII pausing
Šedý et al., J Immunol 2013
(Inflammation) :
CD160 Activation by Herpesvirus Entry
Mediator Augments Inflammatory Cytokine Production and Cytolytic Function by NK Cells
Liou et al., PloS one 2013
(Osteoporosis) :
In addition, KMUP-1 inhibited
RANKL induced activation of signaling molecules ( Akt, MAPKs, calcium and NF-?B ), mRNA expression of osteoclastogensis associated genes (
TRAP , MMP-9, Fra-1, and cathepsin K ) and transcription factors ( c-Fos and NFATc1 )
Pan et al., Neuroendocrinology 1986
:
In the
ARC , however,
CCK-8S may
play some functional roles that are influenced by estrogen
Newman et al., Endocrinology 1985
:
Mediator generation was rapid, with a half-time of approximately 45 sec and was
insulin dose
dependent
Shankar et al., J Biol Chem 1994
:
Furthermore, the
stimulation of
E-selectin cell surface expression and the steady-state E-selectin mRNA levels by thrombin and
TRAP were comparable ... Northern analysis, however, revealed that
TRAP at 100 microM
stimulated PDGF-A and -B chain mRNA expression to a level similar to that induced by thrombin ... Northern analysis, however, revealed that
TRAP at 100 microM
stimulated PDGF-A and -B chain mRNA expression to a level similar to that induced by thrombin
Korthäuer et al., Nature 1993
(Hypergammaglobulinemia...) :
The resultant failure of
TRAP to interact with CD40 on functionally intact B cells is
responsible for the observed immunoglobulin isotype defect in
HIGM1
Nakamura et al., Am J Physiol 1995
:
Plasmin inhibited the thrombin evoked increase in cytosolic
Ca2+ and also
inhibited the Ca2+ response to the tethered peptide
TRAP-6 of the thrombin receptor
Kruse et al., Am J Physiol 1995
:
Receptor operated
effects of alpha-thrombin and of the thrombin receptor activating peptide
TRAP14 on cytoplasmic
Ca2+ concentration ([Ca2+]i) were examined in fura 2-loaded endothelial cells
Kalra et al., Brain Res 1994
:
The results showed that
IL-1 beta increased NKA-li selectively in the median eminence ( ME ) and
arcuate nucleus (ARC) of castrated rats only. ( ABSTRACT TRUNCATED AT 250 WORDS )
Maruyama et al., Biochem Biophys Res Commun 1994
:
TRAP induced rapid morphological changes in HUVECs, with marked increase in the release of prostacyclin,
endothelin , platelet activating factor, tissue type plasminogen activator, and plasminogen activator inhibitor-1
de la Piedra et al., Horm Metab Res 1993
(Bone Resorption) :
In the present work, 10 ( -7 ) M
PTH ( 1-34 ), 10 ( -7 ) M PTHrP ( 1-34 ) and 10 ( -8 ) M or 10 ( -10 ) M 1,25 ( OH ) 2D3 produced a significant
increase in
TRAP activity, when these agonists were added to the calvaria culture
Kasono et al., Bone Miner 1993
(Bone Resorption) :
The minimum effective inhibitory concentration was 0.01 ng/ml, and 1 ng/ml
IL-4 completely
inhibited TRAP ( + ) MNC formation
Jenkins et al., J Cell Sci 1995
:
The use of alanine substituted peptides demonstrated that the
Ca2+ response was
due to
TRAP stimulation of a receptor other than the proteolytically activated thrombin receptor
Kanthou et al., Thromb Haemost 1995
:
Examination of thrombin and TRAP treated cells by immunofluorescence staining followed by computer assisted image analysis revealed that thrombin and to a lesser extent
TRAP induced
PDGF-AA protein expression
Michelson et al., Blood 1996
:
First, although only the GPIb alpha subunit of this putative complex is known to be directly linked to the platelet cytoskeleton via actin binding protein, cytochalasin B inhibited the ADP/epinephrine-, cathepsin G-, and
TRAP induced decrease in platelet surface
GPV
Jiang et al., Circ Res 1996
:
Differences in the kinetics and magnitude of thrombin- and TRAP dependent inositol phosphate ( IP ) accumulation are paralleled by differences in the kinetics and magnitude of thrombin- and
TRAP dependent activation of
MAPK
Blackhart et al., J Biol Chem 1996
:
PAR-2 was also found to be
responsive to
TRAP ( EC50 = 1 microM ) but was unresponsive to Xenopus TRAP ( 50 microM )
Satoh et al., Biochem Biophys Res Commun 1996
:
Both thrombin and
TRAP induced translocation of p60c-src and
p54/58lyn to cytoskeleton in an aggregation dependent manner ... Both thrombin and
TRAP induced translocation of p60c-src and
p54/58lyn to cytoskeleton in an aggregation dependent manner ... Both thrombin and
TRAP induced translocation of
p60c-src and p54/58lyn to cytoskeleton in an aggregation dependent manner ... In contrast,
TRAP , even at concentrations as high as 100 mu M, did not
induce p72syk translocation to cytoskeleton
Faraday et al., Thromb Haemost 1997
:
Similarly, the number of
GPIIb-IIIa receptors capable of binding PAC-1 in
response to ADP and
TRAP was 50 % to 80 % greater in women than men
Minami et al., J Endocrinol 1997
:
Together with the results of our previous studies showing that c-fos gene expression was induced by systemic administration of GH and that GH receptor mRNA was contained in somatostatin neurons in the PeV and NPY neurons in the ARC, the data of the present study indicate that GH, but not
IGF-I ,
acts on the cells in the
ARC and the PeV or in their vicinity to inhibit its own secretion, presumably by activating the somatostatin and NPY neurons
Lin et al., Sheng Li Xue Bao 1996
:
In this group, brain
ANP increased in the periventricular nuclues ( PVN ) and
arcute nucleus (Arc) ( P < 0.05 )
Sahu et al., Endocrinology 1998
:
In addition, in the
ARC and MPOA, the other hypothalamic sites associated with induction of LH surge,
NPY levels
increased before and during the LH surge in young rats, no change in NPY levels in these nuclei was observed in association with the attenuated LH surge in MA rats
Kim et al., Brain Res 1998
(Hyperphagia) :
Animals receiving the HPD ad libitum consumed more calories and gained more weight than animals receiving the BCD ( P < 0.001 ). The
HPD did not
affect ARC NPY mRNA levels, whether the subjects were allowed to overeat or pair fed to the BCD ( P > 0.05 )
Xirasagar et al., J Biol Chem 1998
:
This conclusion is based on the
effects of temperature and
Mg2+ on the affinity of
TRAP for RNAs with CC spacers combined with UV hyperchromicity and circular dichroism
Elias et al., Neuron 1998
(Body Weight) :
We found that
leptin activates neurons in the retrochiasmatic area ( RCA ) and lateral
arcuate nucleus (Arc) that innervate the thoracic spinal cord and also contain cocaine- and amphetamine regulated transcript ( CART )
Han et al., Mol Cell Biol 1999
:
The multisubunit
Mediator complex of Saccharomyces cerevisiae is
required for most
RNA polymerase II (Pol II) transcription