| Literature DB >> 28636428 |
Luis A Gonano1, Peter P Jones1.
Abstract
Ryanodine Receptors (RyRs) are intracellular Ca2+ channels that mediate Ca2+ flux from the sarco(endo)plasmic reticulum in many cell types. The interaction of RyRs with FK506-binding proteins (FKBPs) has been proposed as an important regulatory mechanism, where the loss of this interaction leads to channel dysfunction. In the heart, phosphorylation of RyR has been suggested to disrupt the RyR-FKBP interaction promoting altered Ca2+ signaling, heart failure and arrhythmias. However, the functional result of FKBP interaction with RyR and how this interaction is regulated remains highly controversial. Recently, high resolution structures of RyR have provided novel aspects to the ongoing debate. This review will discuss the most recent functional data in light of these new structures.Entities:
Keywords: CPVT; FKBP; Ryanodine Receptor; SR Ca leak; arrhythmias; heart failure
Mesh:
Substances:
Year: 2017 PMID: 28636428 PMCID: PMC5626368 DOI: 10.1080/19336950.2017.1344799
Source DB: PubMed Journal: Channels (Austin) ISSN: 1933-6950 Impact factor: 2.581