Adenosine A2B receptor signaling
Adenosine A2B
receptor influences cell differentiation and proliferation.
A2B receptors are G-protein-coupled receptors coupling to
classical second messenger pathways, such as modulation of Cyclic Adenosine
3',5'-phosphate (cAMP)
production or the Phospholipase C (PLC)
pathway.
Adenosine A2B receptor interacts with
trimeric G-protein alpha-s/G-protein beta/gamma
and G-protein alpha-q/G-protein
beta/gamma. This causes exchange of GDP for GTP bound to G protein alpha
subunits and subsequent dissociation of G-protein beta/gamma
heterodimers.
G-protein alpha-s activates
Adenylate cyclase I, which then increases levels of
cAMP in the cell and activates Protein kinase cAMP-dependent
(PKA) inactive complex that results in the activation of
PKA [1]. In turn,
PKA phosphorylates and inactivates Glycogen synthase kinase
3 beta (GSK3 beta), which leads
to attenuation of Beta-catenin inhibition. Consequently,
this signaling cascade activates cell cycle progression, initiating activity of
Transcription factor 7-like 2 (TCF7L2 (TCF4))
that promotes the expression of Cyclin D1 and V-myc myelocytomatosis viral
oncogene homolog (c-Myc) [2]. Phosphorylation and activation of cAMP
responsive element binding protein 1 (CREB1) is mainly
mediated via adenosine Adenosine A2B receptor [3].
Adenosine stimulates Interleukin 6
(IL-6) expression in human astrocytoma cell lines via
Adenosine A2B receptor inducing p38 mitogen-activated
protein kinases (p38MAPK). G-protein
alpha-q/11 activates Phospholipase C beta
(PLC-beta). PLC-beta catalyzes
hydrolysis of Phosphoinositide 4,5-bisphosphate (PI(4,5)P2)
into Inositol 1,4,5-triphosphate (IP3) and Diacylglycerol
(DAG). IP3 released into the
cytoplasm mobilizes Ca(II) from internal stores, whereas
DAG activates Protein kinase C epsilon
(PKC-epsilon). PKC-epsilon
induces PTK2B protein tyrosine kinase 2 beta (PYK2)
activation and stimulation of
PKC-epsilon/PYK2/Vav 1 guanine
nucleotide exchange factor (VAV-1)/ Cell division cycle 42
(Cdc42)/Mitogen-activated protein kinase kinase kinase 4
(MEKK4)/Mitogen-activated protein kinase kinase 3
(MEK3) pathway [4]. Stimulation of
Adenosine A2B receptor can activate
p38MAPK via
cAMP/PKA/ Rho guanine
nucleotide exchange factor 7 (BETA-PIX) pathway [5]. p38MAPK, possibly Nuclear factor kappa
B (NF-kB),
and CCAAT/enhancer binding protein beta
(C/EBPbeta) activate
transcription of IL-6 [6].
Human Adenosine A2B receptors mediate
phosphorylation and activation of the Extracellular signal-regulated kinase
(ERK) via cAMP/Rap guanine
nucleotide exchange factor 3 (AMP-GEF1)/RAP1A member of RAS
oncogene family (RAP-1A)/Small
nuclear ribonucleoprotein polypeptide E (B-Raf) pathway
[5].
Adenosine induces NO production by Nitric
oxide synthase 3 (eNOS), whose activation is initiated by
Phosphoinositide-3-kinase (PI3K)/V-akt murine thymoma viral
oncogene homolog 1 (AKT(PKB)) pathway and
ERK/ ELK1 member of ETS oncogene family
(Elk-1)-dependent transcription. Upon activation by
cAMP, guanine nucleotide exchange factor Rap guanine
nucleotide exchange factor 2 (PDZ-GEF) stimulates
PI3K activation via v-Ha-ras Harvey rat sarcoma viral
oncogene homolog (H-Ras). PI3K
converts Phosphatidylinositol 4,5-biphosphate
(PtdIns(4,5)P2) to Phosphatidylinositol 3,4,5-triphosphate
(PtdIns(3,4,5)P3) [7].
PtdIns(3,4,5)P3 is a second messenger that directly binds to
and AKT. AKT phosphorylates and
activates eNOS [8].
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Evidence for involvement of Wnt signaling pathway in IB-MECA mediated suppression of melanoma cells.
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Adenosine A 2B receptors modulate cAMP levels and induce CREB but not ERK1/2 and p38 phosphorylation in rat skeletal muscle cells.
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IL-6 expression induced by adenosine A2b receptor stimulation in U373 MG cells depends on p38 mitogen activated kinase and protein kinase C.
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The G(s)-coupled adenosine A(2B) receptor recruits divergent pathways to regulate ERK1/2 and p38.
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