J Neurochem 2002,
PMID: 12065651
Ang, Kok-Long; Antoni, Ferenc A
The hydrolysis of cyclic nucleotide second messengers takes place through multiple cyclic nucleotide phosphodiesterases (PDEs). The significance of this diversification is not fully understood. Here we report the differential regulation of low K(m) Ca2+-activated (PDE1C) and Ca2+-independent, rolipram-sensitive (PDE4) PDEs by protein phosphorylation in the neuroendocrine cell line AtT20. Incubation of cells with 8-(4-chlorophenylthio)-cyclic AMP (CPT-cAMP) enhanced PDE4 and reduced PDE1C activity. These effects were blocked by H89 indicating mediation by cAMP-dependent protein kinase (PKA), furthermore in broken cell preparations PKA produced the same reciprocal changes of PDE activities. Calyculin A, an inhibitor of protein phosphatases 1 and 2 A, stimulated PDE4 and enhanced the inhibitory effect of CPT-cAMP on PDE1C. The reduction of PDE1C activity was characterized by a marked attenuation of the activation by Ca2+/calmodulin. Stimulation of PDE4 activity by CPT-cAMP or calyculin A was attributable to PDE4D3 and these effects could also be reproduced in human embryonic kidney cells expressing epitope-tagged PDE4D3. Together, these data show reciprocal regulation of PDE1C and PDE4D by PKA, which represents a novel scheme for plasticity in intracellular signalling.
Diseases/Pathways annotated by Medline MESH: Second Messenger Systems
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Text Mining Data
PDE1C — PKA: "
Together, these data show reciprocal
regulation of
PDE1C and PDE4D by
PKA , which represents a novel scheme for plasticity in intracellular signalling
"
PDE4D — PKA: "
Together, these data show reciprocal regulation of PDE1C and PDE4D by PKA , which represents a novel scheme for plasticity in intracellular signalling
"
Manually curated Databases
No curated data.