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Verfasst von:Chen, Jian [VerfasserIn]   i
 Chen, Kun [VerfasserIn]   i
 Sroubek, Jakub [VerfasserIn]   i
 Wu, Zhi-Yuan [VerfasserIn]   i
 Thomas, Dierk [VerfasserIn]   i
 Bian, Jin-Song [VerfasserIn]   i
 McDonald, Thomas V. [VerfasserIn]   i
Titel:Post-transcriptional control of human ether-a-go-go-related gene potassium channel protein by alpha-adrenergic receptor stimulation
Verf.angabe:Jian Chen, Kun Chen, Jakub Sroubek, Zhi-Yuan Wu, Dierk Thomas, Jin-Song Bian, and Thomas V. McDonald
E-Jahr:2010
Jahr:July 14, 2010
Umfang:12 S.
Fussnoten:Gesehen am 03.03.2023
Titel Quelle:Enthalten in: Molecular pharmacology
Ort Quelle:Bethesda, Md. : ASPET, 1965
Jahr Quelle:2010
Band/Heft Quelle:78(2010), 2, Seite 186-197
ISSN Quelle:1521-0111
Abstract:Stimulation of alpha1-adrenoreceptors (alpha1-AR) acutely alters ion channel behavior via several signaling pathways [calcium and protein kinase C (PKC)]. Little is known about sustained alpha1-adrenergic/PKC signaling and channel regulation as may occur during cardiovascular disease states. Here we describe the effects of prolonged alpha1A-AR and PKC activity on human ether-a-go-go-related gene (HERG) K(+) channels (Kv11.1) expressed in a heterologous expression system. Stimulation of alpha1A-AR with phenylephrine or direct activation of PKC with phorbol ester increased HERG channel protein abundance and K(+) current density in a time- and dose-dependent manner. Channel augmentation reached a steady-state plateau within 24 h with a 2- to 6-fold induction. Phorbol ester and moderate alpha1A-AR stimulation enhanced HERG abundance in a PKC-dependent fashion but with stronger alpha1A-adrenergic stimulation; protein kinase A (PKA)-dependent activity also contributed. Comparable channel induction of other cardiac K(+) channels was not seen in this system. Comparison of wild-type HERG and channels with either mutated PKC phosphorylation sites (HERGDeltaPKC) or mutated PKA phosphorylation sites (HERGDeltaPKA) suggested that the mechanisms of augmentation of HERG by the two kinases were partially overlapping. The PKC-dependent effect was largely due to enhanced synthetic rates. Stimulation of alpha1-AR in cultured rat neonatal cardiac myocytes also enhanced the abundance of ERG channels. These findings show that alpha1A-AR stimulation is capable of influencing the balance of HERG channel synthesis and degradation via multiple signaling pathways, a process that may have relevance in cardiac diseases and treatment.
DOI:doi:10.1124/mol.109.062216
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1124/mol.109.062216
 DOI: https://doi.org/10.1124/mol.109.062216
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Adrenergic alpha-1 Receptor Agonists
 Adrenergic alpha-Agonists
 Animals
 Blotting, Western
 Cell Line
 ERG1 Potassium Channel
 Ether-A-Go-Go Potassium Channels
 Humans
 Phenylephrine
 Phosphorylation
 Protein Kinase C
 Rats
 RNA Processing, Post-Transcriptional
 Signal Transduction
 Tetradecanoylphorbol Acetate
K10plus-PPN:1838102264
Verknüpfungen:→ Zeitschrift

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