| Literature DB >> 28965170 |
Elise Balse1, Catherine Eichel2.
Abstract
Activation of the electrical signal and its transmission as a depolarizing wave in the whole heart requires highly organized myocyte architecture and cell-cell contacts. In addition, complex trafficking and anchoring intracellular machineries regulate the proper surface expression of channels and their targeting to distinct membrane domains. An increasing list of proteins, lipids, and second messengers can contribute to the normal targeting of ion channels in cardiac myocytes. However, their precise roles in the electrophysiology of the heart are far from been extensively understood. Nowadays, much effort in the field focuses on understanding the mechanisms that regulate ion channel targeting to sarcolemma microdomains and their organization into macromolecular complexes. The purpose of the present section is to provide an overview of the characterized partners of the main cardiac sodium channel, NaV1.5, involved in regulating the functional expression of this channel both in terms of trafficking and targeting into microdomains.Entities:
Keywords: Ankyrin G; CASK; Caveolin; Connexin 43; Desmoglein 2; Desmoplakin; Dystrophin-syntrophin complex; Myocyte membrane domains; NaV1.5 protein partners; Plakoglobin; Plakophilin 2; SAP97
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Year: 2018 PMID: 28965170 DOI: 10.1007/164_2017_45
Source DB: PubMed Journal: Handb Exp Pharmacol ISSN: 0171-2004