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Rottlerin inhibits stimulated enzymatic secretion and several intracellular signaling transduction pathways in pancreatic acinar cells by a non-PKC-δ-dependent mechanism
- Source :
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. (1):25-38
- Publisher :
- Elsevier B.V.
-
Abstract
- Protein kinase C-delta (PKC-delta) becomes activated in pancreatic acini in response to cholecystokinin (CCK) and plays a pivotal role in the exocrine pancreatic secretion. Rottlerin, a polyphenolic compound, has been widely used as a potent and specific PKC-delta inhibitor. However, some recent studies showed that rottlerin was not effective in inhibiting PKCdelta activity in vitro and that may display unspecific effects. The aims of this work were to investigate the specificity of rottlerin as an inhibitor of PKC-delta activity in intact cells and to elucidate the biochemical causes of its unspecificity. Preincubation of pancreatic acini with rottlerin (6 microM) inhibited CCK-stimulated translocation, tyrosine phosphorylation (TyrP) and activation of PKC-delta in pancreatic acini in a time-dependent manner. Rottlerin inhibited amylase secretion stimulated by both PKC-dependent pathways (CCK, bombesin, carbachol, TPA) and also by PKC-independent pathways (secretin, VIP, cAMP analogue). CCK-stimulation of MAPK activation and p125(FAK) TyrP which are mediated by PKC-dependent and -independent pathways were also inhibited by rottlerin. Moreover, rottlerin rapidly depleted ATP content in pancreatic acini in a similar way as the mitochondrial uncouplers CCCP and FCCP. All studied inhibitory effects of rottlerin in pancreatic acini were mimicked by FCCP (agonists-stimulated amylase secretion, p125(FAK) TyrP, MAPK activation and PKC-delta TyrP and translocation). Finally, rottlerin as well as FCCP display a potent inhibitory effect on the activation of other PKC isoforms present in pancreatic acini. Our results suggest that rottlerin effects in pancreatic acini are not due to a specific PKC-delta blockade, but likely due to its negative effect on acini energy resulting in ATP depletion. Therefore, to study the role of PKC-delta in cellular processes using rottlerin it is essential to keep in mind that may deplete ATP levels and inhibit different PKC isoforms. Our results give reasons for a more careful choice of rottlerin for PKC-delta investigation.
- Subjects :
- Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone
Male
Carbonyl Cyanide m-Chlorophenyl Hydrazone
Cell Survival
Pancreatic acini
Biology
digestive system
Secretin
chemistry.chemical_compound
Adenosine Triphosphate
Protein kinase C
medicine
Animals
Protein Isoforms
Secretion
Benzopyrans
Phosphorylation
Rats, Wistar
Protein kinase A
Molecular Biology
Exocrine secretion
Bombesin
Acetophenones
Tyrosine phosphorylation
Cell Biology
PKC inhibitors
Pancreas, Exocrine
Peptide Fragments
Cell biology
Mitochondria
Rats
Receptor, Cholecystokinin A
Rottlerin
Protein Kinase C-delta
Protein Transport
medicine.anatomical_structure
chemistry
Biochemistry
Focal Adhesion Kinase 1
Amylases
Tyrosine
Mitogen-Activated Protein Kinases
Pancreas
Cholecystokinin
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 01674889
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
- Accession number :
- edsair.doi.dedup.....fe14236b3f541bb28e61494906f58027
- Full Text :
- https://doi.org/10.1016/j.bbamcr.2005.10.007