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EPHB2 — UCN
Text-mined interactions from Literome
Brar et al., J Biol Chem 2000
(MAP Kinase Signaling System...) :
UCN caused rapid phosphorylation of
ERK1/2-p42/44 , and PD98059, which blocks the MEK1-ERK1/2-p42/44 cascade, also
inhibited the survival promoting effect of
UCN
Papadopoulou et al., Mol Endocrinol 2004
:
We found that the adenylyl cyclase/PKA pathway has the capacity to markedly decrease
UCN induced
ERK1/2 activation, and that these effects were due in part to the ability of PKA to phosphorylate the CRH-R1alpha at position Ser ( 301 ) in the third intracellular loop
Brar et al., Endocrinology 2004
:
Using Chinese hamster ovary cells stably expressing CRFR1 and CRFR2beta, we show that
Ucn-I , Ucn-II and Ucn-III
activate ERK1/2-p42 , 44 via CRFR2beta ... CRF and
Ucn-I but not Ucn-II or Ucn-III
activates ERK1/2-p42 , 44 in Chinese hamster ovary cells stably expressing CRFR1 ... Use of the G ( i ) and G ( o ) protein inhibitor pertussis toxin showed that
ERK1/2-p42 , 44 activation by
Ucn-I via CRFR1 and CRFR2beta are both G ( i ) and/or G ( o ) protein
dependent
Pei et al., Mol Pharmacol 2006
(Multiple Myeloma) :
They also suggest a role for Chk1 in
UCN-01 induced
ERK1/2 activation, implying the existence of a heretofore unrecognized link between Chk1 and ERK1/2 signaling
Punn et al., Mol Endocrinol 2006
:
In human embryonic kidney 293 cells overexpressing recombinant CRH-R1alpha,
UCN I
induced ERK1/2 and p38 MAPK activation was dependent on signaling molecules involved in agonist induced CRH-R1alpha trafficking and endocytosis
Kageyama et al., Mol Cell Endocrinol 2007
:
Bisindolylmaleimide partially inhibited the
UCN mediated decrease in
ERK phosphorylation in A7r5 cells, suggesting that the protein kinase C pathway is partially involved in CRF2 receptor signal transduction
Wu et al., Endocrinology 2007
:
Ucn 1 and Ucn 2
stimulated dose dependent cAMP production and
ERK1/2 phosphorylation in the esophageal cells, whereas CRF and CRF1 agonist, cortagine, had less potent effects
Huang et al., J Mol Endocrinol 2009
:
Urocortin induces interleukin-6 release from rat cardiomyocytes through p38 MAP kinase,
ERK and NF-kappaB activation ...
Ucn stimulates activation of
ERK and p38 MAP kinases, while both MEK1 and p38 inhibitor block Ucn induced IL-6 release ... Finally, the CRH-R antagonists alpha-helical ( 9-41 ) CRH and astressin-2B completely inhibit
Ucn induced IL-6 release, as well as activation of
ERK , p38, and NF-kappaB
Yuan et al., Mol Cell Endocrinol 2010
:
We discovered that a non-receptor tyrosine kinase, Src, is involved in the
urocortin induced activation of
ERK1/2 in mouse atrial HL-1 myocytes ... The selective Src family kinase inhibitor, PP2, reduced the
urocortin induced phosphorylation of
ERK1/2 , and so did the expression of a dominant negative mutant of Src in transfected HL-1 cells
Wu et al., Endocrinology 2011
:
CRH and
Ucn-1 , but not Ucn-2,
stimulated significant
ERK1/2 phosphorylation