Disruption of the cyclic AMP phosphodiesterase-4 (PDE4)-HSP20 complex attenuates the β-agonist induced hypertrophic response in cardiac myocytes (Q39589356)

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scientific article published on 18 February 2011

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English	Disruption of the cyclic AMP phosphodiesterase-4 (PDE4)-HSP20 complex attenuates the β-agonist induced hypertrophic response in cardiac myocytes	scientific article published on 18 February 2011

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scholarly article

1 reference

Europe PubMed Central

13 September 2017

Disruption of the cyclic AMP phosphodiesterase-4 (PDE4)-HSP20 complex attenuates the β-agonist induced hypertrophic response in cardiac myocytes (English)

1 reference

Europe PubMed Central

13 September 2017

Miles D. Houslay

9

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Europe PubMed Central

13 September 2017

Frank Christian

object named as

F Christian

5

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Manuela Zaccolo

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M Zaccolo

8

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author name string

Y Y Sin

1

1 reference

Europe PubMed Central

13 September 2017

H V Edwards

2

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Europe PubMed Central

13 September 2017

X Li

3

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Europe PubMed Central

13 September 2017

J P Day

4

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Europe PubMed Central

13 September 2017

A J Dunlop

6

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Europe PubMed Central

13 September 2017

D R Adams

7

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Europe PubMed Central

13 September 2017

G S Baillie

10

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Europe PubMed Central

13 September 2017

publication date

18 February 2011

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Europe PubMed Central

13 September 2017

Journal of Molecular and Cellular Cardiology

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Europe PubMed Central

13 September 2017

50

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Europe PubMed Central

13 September 2017

5

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Europe PubMed Central

13 September 2017

872-883

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Europe PubMed Central

13 September 2017

Small heat shock proteins in smooth muscle

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Blockade of Hsp20 phosphorylation exacerbates cardiac ischemia/reperfusion injury by suppressed autophagy and increased cell death

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The small heat shock proteins and their role in human disease.

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The human genome encodes 10 alpha-crystallin-related small heat shock proteins: HspB1-10

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Small heat shock proteins associated with cerebral amyloid angiopathy of hereditary cerebral hemorrhage with amyloidosis (Dutch type) induce interleukin-6 secretion.

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Small heat-shock protein Hsp20 attenuates beta-agonist-mediated cardiac remodeling through apoptosis signal-regulating kinase 1

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Small heat-shock protein Hsp20 phosphorylation inhibits beta-agonist-induced cardiac apoptosis

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The small heat shock protein (HSP) 20 is dynamically associated with the actin cross-linking protein actinin.

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Localization, macromolecular associations, and function of the small heat shock-related protein HSP20 in rat heart

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Hsp20 and its cardioprotection

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Human mutation in the anti-apoptotic heat shock protein 20 abrogates its cardioprotective effects

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PDE5A suppression of acute beta-adrenergic activation requires modulation of myocyte beta-3 signaling coupled to PKG-mediated troponin I phosphorylation

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Cyclic adenosine monophosphate in acute myocardial infarction with heart failure: slayer or savior?

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VIP induces PKA-mediated rapid and sustained phosphorylation of HSP20.

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Evidence that a protein kinase A substrate, small heat-shock protein 20, modulates myometrial relaxation in human pregnancy.

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Transducible heat shock protein 20 (HSP20) phosphopeptide alters cytoskeletal dynamics

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Phosphorylation and activation of a transducible recombinant form of human HSP20 in Escherichia coli

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Compartmentalized signalling: spatial regulation of cAMP by the action of compartmentalized phosphodiesterases.

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Regulation by phosphodiesterase isoforms of protein kinase A-mediated attenuation of myocardial protein kinase D activation

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Spatiotemporal dynamics of beta-adrenergic cAMP signals and L-type Ca2+ channel regulation in adult rat ventricular myocytes: role of phosphodiesterases

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Keynote review: phosphodiesterase-4 as a therapeutic target

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cAMP-Specific phosphodiesterase-4 enzymes in the cardiovascular system: a molecular toolbox for generating compartmentalized cAMP signaling

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The unique amino-terminal region of the PDE4D5 cAMP phosphodiesterase isoform confers preferential interaction with beta-arrestins

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Targeting of cyclic AMP degradation to beta 2-adrenergic receptors by beta-arrestins

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beta-Arrestin-mediated PDE4 cAMP phosphodiesterase recruitment regulates beta-adrenoceptor switching from Gs to Gi

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Phosphodiesterase 4D deficiency in the ryanodine-receptor complex promotes heart failure and arrhythmias

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Mdm2 directs the ubiquitination of beta-arrestin-sequestered cAMP phosphodiesterase-4D5

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Novel single chain cAMP sensors for receptor-induced signal propagation.

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Mapping binding sites for the PDE4D5 cAMP-specific phosphodiesterase to the N- and C-domains of beta-arrestin using spot-immobilized peptide arrays

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Long PDE4 cAMP specific phosphodiesterases are activated by protein kinase A-mediated phosphorylation of a single serine residue in Upstream Conserved Region 1 (UCR1)

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PKA-phosphorylation of PDE4D3 facilitates recruitment of the mAKAP signalling complex

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10.1016/J.YJMCC.2011.02.006

1 reference

Europe PubMed Central

13 September 2017

1 reference

Europe PubMed Central

13 September 2017

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