Fluorescence resonance energy transfer-based analysis of cAMP dynamics
in live neonatal rat cardiac myocytes reveals distinct functions
of compartmentalized phosphodiesterases
M. Mongillo, T. McSorley, S. Evellin, A. Sood, V. Lissandron, A. Terrin, E. Huston, A. Hannawacker, M. Lohse, T. Pozzan, M. Houslay, and M. Zaccolo. Circ Res, 95 (1):
67-75(July 2004)Mongillo, Marco McSorley, Theresa Evellin, Sandrine Sood, Arvind
Lissandron, Valentina Terrin, Anna Huston, Elaine Hannawacker, Annette
Lohse, Martin J Pozzan, Tullio Houslay, Miles D Zaccolo, Manuela
Research Support, Non-U.S. Gov't United States Circulation research
Circ Res. 2004 Jul 9;95(1):67-75. Epub 2004 Jun 3..
Abstract
Cardiac myocytes have provided a key paradigm for the concept of the
compartmentalized cAMP generation sensed by AKAP-anchored PKA. Phosphodiesterases
(PDEs) provide the sole route for degrading cAMP in cells and are
thus poised to regulate intracellular cAMP gradients. PDE3 and PDE4
represent the major cAMP degrading activities in rat ventriculocytes.
By performing real-time imaging of cAMP in situ, we establish the
hierarchy of these PDEs in controlling cAMP levels in basal conditions
and on stimulation with a beta-adrenergic receptor agonist. PDE4,
rather than PDE3, appears to be responsible for modulating the amplitude
and duration of the cAMP response to beta-agonists. PDE3 and PDE4
localize to distinct compartments and this may underpin their different
functional roles. Our findings indicate the importance of distinctly
localized PDE isoenzymes in determining compartmentalized cAMP signaling.
Fluorescence resonance energy transfer-based analysis of cAMP dynamics
in live neonatal rat cardiac myocytes reveals distinct functions
of compartmentalized phosphodiesterases
Mongillo, Marco McSorley, Theresa Evellin, Sandrine Sood, Arvind
Lissandron, Valentina Terrin, Anna Huston, Elaine Hannawacker, Annette
Lohse, Martin J Pozzan, Tullio Houslay, Miles D Zaccolo, Manuela
Research Support, Non-U.S. Gov't United States Circulation research
Circ Res. 2004 Jul 9;95(1):67-75. Epub 2004 Jun 3.
%0 Journal Article
%1 Mongillo2004
%A Mongillo, M.
%A McSorley, T.
%A Evellin, S.
%A Sood, A.
%A Lissandron, V.
%A Terrin, A.
%A Huston, E.
%A Hannawacker, A.
%A Lohse, M. J.
%A Pozzan, T.
%A Houslay, M. D.
%A Zaccolo, M.
%D 2004
%J Circ Res
%K & 3 3',5'-Cyclic-AMP 4 AMP/*metabolism Adrenergic Animals Animals, Cardiac/*enzymology Cyclic Energy Fluorescence Inhibitors/pharmacology Myocytes, Newborn Norepinephrine/pharmacology Nucleotide Phosphodiesterase Phosphodiesterases, Phosphodiesterases/analysis/antagonists Rats Resonance Transfer Type alpha-Agonists/pharmacology inhibitors/*physiology
%N 1
%P 67-75
%T Fluorescence resonance energy transfer-based analysis of cAMP dynamics
in live neonatal rat cardiac myocytes reveals distinct functions
of compartmentalized phosphodiesterases
%U http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=15178638
%V 95
%X Cardiac myocytes have provided a key paradigm for the concept of the
compartmentalized cAMP generation sensed by AKAP-anchored PKA. Phosphodiesterases
(PDEs) provide the sole route for degrading cAMP in cells and are
thus poised to regulate intracellular cAMP gradients. PDE3 and PDE4
represent the major cAMP degrading activities in rat ventriculocytes.
By performing real-time imaging of cAMP in situ, we establish the
hierarchy of these PDEs in controlling cAMP levels in basal conditions
and on stimulation with a beta-adrenergic receptor agonist. PDE4,
rather than PDE3, appears to be responsible for modulating the amplitude
and duration of the cAMP response to beta-agonists. PDE3 and PDE4
localize to distinct compartments and this may underpin their different
functional roles. Our findings indicate the importance of distinctly
localized PDE isoenzymes in determining compartmentalized cAMP signaling.
@article{Mongillo2004,
abstract = {Cardiac myocytes have provided a key paradigm for the concept of the
compartmentalized cAMP generation sensed by AKAP-anchored PKA. Phosphodiesterases
(PDEs) provide the sole route for degrading cAMP in cells and are
thus poised to regulate intracellular cAMP gradients. PDE3 and PDE4
represent the major cAMP degrading activities in rat ventriculocytes.
By performing real-time imaging of cAMP in situ, we establish the
hierarchy of these PDEs in controlling cAMP levels in basal conditions
and on stimulation with a beta-adrenergic receptor agonist. PDE4,
rather than PDE3, appears to be responsible for modulating the amplitude
and duration of the cAMP response to beta-agonists. PDE3 and PDE4
localize to distinct compartments and this may underpin their different
functional roles. Our findings indicate the importance of distinctly
localized PDE isoenzymes in determining compartmentalized cAMP signaling.},
added-at = {2010-12-14T18:12:02.000+0100},
author = {Mongillo, M. and McSorley, T. and Evellin, S. and Sood, A. and Lissandron, V. and Terrin, A. and Huston, E. and Hannawacker, A. and Lohse, M. J. and Pozzan, T. and Houslay, M. D. and Zaccolo, M.},
biburl = {https://www.bibsonomy.org/bibtex/213ddf7b1cc3becaccba8b981bb258031/pharmawuerz},
endnotereftype = {Journal Article},
interhash = {17189a3f99bd287a8c61009489af6f5c},
intrahash = {13ddf7b1cc3becaccba8b981bb258031},
issn = {1524-4571 (Electronic) 1524-4571 (Linking)},
journal = {Circ Res},
keywords = {& 3 3',5'-Cyclic-AMP 4 AMP/*metabolism Adrenergic Animals Animals, Cardiac/*enzymology Cyclic Energy Fluorescence Inhibitors/pharmacology Myocytes, Newborn Norepinephrine/pharmacology Nucleotide Phosphodiesterase Phosphodiesterases, Phosphodiesterases/analysis/antagonists Rats Resonance Transfer Type alpha-Agonists/pharmacology inhibitors/*physiology},
month = {Jul 9},
note = {Mongillo, Marco McSorley, Theresa Evellin, Sandrine Sood, Arvind
Lissandron, Valentina Terrin, Anna Huston, Elaine Hannawacker, Annette
Lohse, Martin J Pozzan, Tullio Houslay, Miles D Zaccolo, Manuela
Research Support, Non-U.S. Gov't United States Circulation research
Circ Res. 2004 Jul 9;95(1):67-75. Epub 2004 Jun 3.},
number = 1,
pages = {67-75},
shorttitle = {Fluorescence resonance energy transfer-based analysis of cAMP dynamics
in live neonatal rat cardiac myocytes reveals distinct functions
of compartmentalized phosphodiesterases},
timestamp = {2010-12-14T18:12:26.000+0100},
title = {Fluorescence resonance energy transfer-based analysis of cAMP dynamics
in live neonatal rat cardiac myocytes reveals distinct functions
of compartmentalized phosphodiesterases},
url = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=15178638},
volume = 95,
year = 2004
}