English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/71046
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE
Exportar a otros formatos:

Title

Metabotropic regulation of RhoA/Rho-associated kinase by l-type Ca2+ Channels: New Mechanism for Depolarization-Evoked Mammalian Arterial Contraction

AuthorsFernández-Tenorio, Miguel; Porras-González, Cristina; Castellano, Antonio; Valle-Rodríguez, Alberto del; López-Barneo, José ; Ureña, Juan
Issue Date2011
PublisherAmerican Heart Association
CitationCirculation Research 108: 1348-1357 (2011)
Abstract[Background] Sustained vascular smooth muscle contraction is mediated by extracellular Ca2+ influx through L-type voltage-gated Ca 2+ channels (VGCC) and RhoA/Rho-associated kinase (ROCK)-dependent Ca2+ sensitization of the contractile machinery. VGCC activation can also trigger an ion-independent metabotropic pathway that involves G-protein/phospholipase C activation, inositol 1,4,5-trisphosphate synthesis, and Ca2+ release from the sarcoplasmic reticulum (calcium channel-induced Ca release). We have studied the functional role of calcium channel-induced Ca release and the inter-relations between Ca2+ channel and RhoA/ROCK activation.
[Methods and results] We have used normal and genetically modified animals to study single myocyte electrophysiology and fluorimetry as well as cytosolic Ca2+ and diameter in intact arteries. These analyses were complemented with measurement of tension and RhoA activity in normal and reversibly permeabilized arterial rings. We have found that, unexpectedly, L-type Ca channel activation and subsequent metabotropic Ca release from sarcoplasmic reticulum participate in depolarization-evoked RhoA/ROCK activity and sustained arterial contraction. We show that these phenomena do not depend on the change in the membrane potential itself, or the mere release of Ca from the sarcoplasmic reticulum, but they require the simultaneous activation of VGCC and the downstream metabotropic pathway with concomitant Ca2+ release. During protracted depolarizations, refilling of the stores by a residual extracellular Ca2+ influx through VGCC helps maintaining RhoA activity and sustained arterial contraction.
[Conclusions] These findings reveal that calcium channel-induced Ca release has a major role in tonic vascular smooth muscle contractility because it links membrane depolarization and Ca channel activation with metabotropic Ca release and sensitization (RhoA/ROCK stimulation). © 2011 American Heart Association, Inc.
Publisher version (URL)http://dx.doi.org/10.1161/CIRCRESAHA.111.240127
URIhttp://hdl.handle.net/10261/71046
DOI10.1161/CIRCRESAHA.111.240127
Identifiersdoi: 10.1161/CIRCRESAHA.111.240127
issn: 0009-7330
Appears in Collections:(IBIS) Artículos
Files in This Item:
File Description SizeFormat 
tenorio_metabotropic.pdf1,94 MBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.