Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
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Query: UMLS:C0030305 (
pancreatitis
)
16,014
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The transcription factor NF-kappaB plays a critical role in inflammatory and cell death responses during acute pancreatitis. Previous studies in our laboratory demonstrated that protein kinase C (PKC) isoforms PKCdelta and epsilon are key regulators of NF-kappaB activation induced by cholecystokinin-8 (CCK-8), tumor necrosis factor-alpha, and ethanol. However, the downstream participants in regulating NF-kappaB activation in exocrine pancreas remain poorly understood. Here, we demonstrate that
protein kinase D1
(
PKD1
) is a key downstream target of PKCdelta and PKCepsilon in pancreatic acinar cells stimulated by two major secretagogues, CCK-8 and the cholinergic agonist carbachol (CCh), and that
PKD1
is necessary for NF-kappaB activation induced by CCK-8 and CCh. Both CCK-8 and CCh dose dependently induced a rapid and striking activation of
PKD1
in rat pancreatic acinar cells, as measured by in vitro kinase assay and by phosphorylation at
PKD1
activation loop (Ser744/748) or autophosphorylation site (Ser916). The phosphorylation and activation of
PKD1
correlated with NF-kappaB activity stimulated by CCK-8 or CCh, as measured by NF-kappaB DNA binding. Either inhibition of PKCdelta or epsilon by isoform-specific inhibitory peptides, genetic deletion of PKCdelta and epsilon in pancreatic acinar cells, or knockdown of
PKD1
by using small interfering RNAs in AR42J cells resulted in a marked decrease in
PKD1
and NF-kappaB activation stimulated by CCK-8 or CCh. Conversely, overexpression of
PKD1
resulted in augmentation of CCK-8- and CCh-stimulated NF-kappaB activation. Finally, the kinetics of
PKD1
and NF-kappaB activation during cerulein-induced rat
pancreatitis
showed that both
PKD1
and NF-kappaB activation were early events during acute pancreatitis and that their time courses of response were similar. Our results identify
PKD1
as a novel early convergent point for PKCdelta and epsilon in the signaling pathways mediating NF-kappaB activation in
pancreatitis
.
...
PMID:Protein kinase D1 mediates NF-kappaB activation induced by cholecystokinin and cholinergic signaling in pancreatic acinar cells. 1884 74