Prolonged AT1R activation induces CaV1.2 channel internalization in rat cardiomyocytes

Tamara Hermosilla, Matías Encina, Danna Morales, Cristian Moreno, Carolina Conejeros, Hilda M. Alfaro-Valdés, Felipe Lagos-Meza, Felipe Simon, Christophe Altier, Diego Varela

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)


The cardiac L-type calcium channel is a multi-subunit complex that requires co-assembling of the pore-forming subunit CaV1.2 with auxiliary subunits CaVα2δ and CaVβ. Its traffic has been shown to be controlled by these subunits and by the activation of various G-protein coupled receptors (GPCR). Here, we explore the consequences of the prolonged activation of angiotensin receptor type 1 (AT1R) over CaV1.2 channel trafficking. Bioluminescence Resonance Energy Transfer (BRET) assay between β-arrestin and L-type channels in angiotensin II-stimulated cells was used to assess the functional consequence of AT1R activation, while immunofluorescence of adult rat cardiomyocytes revealed the effects of GPCR activation on CaV1.2 trafficking. Angiotensin II exposure results in β-arrestin1 recruitment to the channel complex and an apparent loss of CaV1.2 immunostaining at the T-tubules. Accordingly, angiotensin II stimulation causes a decrease in L-type current, Ca2+ transients and myocyte contractility, together with a faster repolarization phase of action potentials. Our results demonstrate that prolonged AT1R activation induces β-arrestin1 recruitment and the subsequent internalization of CaV1.2 channels with a half-dose of AngII on the order of 100 nM, suggesting that this effect depends on local renin-angiotensin system. This novel AT1R-dependent CaV1.2-trafficking modulation likely contributes to angiotensin II-mediated cardiac remodeling.

Original languageEnglish
Article number10131
JournalScientific Reports
Issue number1
Publication statusPublished - 1 Dec 2017

ASJC Scopus subject areas

  • General


Dive into the research topics of 'Prolonged AT1R activation induces CaV1.2 channel internalization in rat cardiomyocytes'. Together they form a unique fingerprint.

Cite this