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Title

Kv1.5-Kvb1.3 Recycling is PKC-Dependent

AuthorsMacías, Álvaro; Cruz, Alicia de la CSIC ORCID; Peraza, Diego A.; Benito-Bueno, Ángela de; González, Teresa; Valenzuela, Carmen CSIC ORCID
KeywordsKV1.5
KVβ1.3
PKC
Calphostin C
RACK1
Bisindolylmaleimide II
Traffic
Issue Date2021
PublisherMultidisciplinary Digital Publishing Institute
CitationInternational Journal of Molecular Sciences 22(3): 1336 (2021)
AbstractKV1.5 channel function is modified by different regulatory subunits. KVβ1.3 subunits assemble with KV1.5 channels and induce a fast and incomplete inactivation. Inhibition of PKC abolishes the KVβ1.3-induced fast inactivation, decreases the amplitude of the current KV1.5–KVβ1.3 and modifies their pharmacology likely due to changes in the traffic of KV1.5–KVβ1.3 channels in a PKC-dependent manner. In order to analyze this hypothesis, HEK293 cells were transfected with KV1.5–KVβ1.3 channels, and currents were recorded by whole-cell configuration of the patch-clamp technique. The presence of KV1.5 in the membrane was analyzed by biotinylation techniques, live cell imaging and confocal microscopy approaches. PKC inhibition resulted in a decrease of 33 ± 7% of channels in the cell surface due to reduced recycling to the plasma membrane, as was confirmed by confocal microscopy. Live cell imaging indicated that PKC inhibition almost abolished the recycling of the KV1.5–KVβ1.3 channels, generating an accumulation of channels into the cytoplasm. All these results suggest that the trafficking regulation of KV1.5–KVβ1.3 channels is dependent on phosphorylation by PKC and, therefore, they could represent a clinically relevant issue, mainly in those diseases that exhibit modifications in PKC activity.
Description© 2021 by the authors.
Publisher version (URL)http://dx.doi.org/10.3390/ijms22031336
URIhttp://hdl.handle.net/10261/242091
DOIhttp://dx.doi.org/10.3390/ijms22031336
ISSN1661-6596
E-ISSN1422-0067
Appears in Collections:(IIBM) Artículos
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