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Junctophilin-2 tethers T-tubules and recruits functional L-type calcium channels to lipid rafts in adult cardiomyocytes
Author(s) -
Claire Poulet,
Jose L. SanchezAlonso,
Pamela Swiatlowska,
Florence Mouy,
Carla Lucarelli,
Anita AlvarezLaviada,
Polina Gross,
Cesare M. Terracciano,
Steven R. Houser,
Julia Gorelik
Publication year - 2020
Publication title -
cardiovascular research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.774
H-Index - 219
eISSN - 1755-3245
pISSN - 0008-6363
DOI - 10.1093/cvr/cvaa033
Subject(s) - ryanodine receptor , endoplasmic reticulum , microbiology and biotechnology , myocyte , voltage dependent calcium channel , biology , calcium , tubule , medicine , endocrinology , chemistry , biophysics , kidney
In cardiomyocytes, transverse tubules (T-tubules) associate with the sarcoplasmic reticulum (SR), forming junctional membrane complexes (JMCs) where L-type calcium channels (LTCCs) are juxtaposed to Ryanodine receptors (RyR). Junctophilin-2 (JPH2) supports the assembly of JMCs by tethering T-tubules to the SR membrane. T-tubule remodelling in cardiac diseases is associated with downregulation of JPH2 expression suggesting that JPH2 plays a crucial role in T-tubule stability. Furthermore, increasing evidence indicate that JPH2 might additionally act as a modulator of calcium signalling by directly regulating RyR and LTCCs. This study aimed at determining whether JPH2 overexpression restores normal T-tubule structure and LTCC function in cultured cardiomyocytes.

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