Ryanodine receptor modification and regulation by intracellular Ca 2+ and Mg 2+ in healthy and failing human hearts

• Published in: Journal of molecular and cellular cardiology Vol. 104; p. 53
• Main Authors: Walweel, K, Molenaar, P, Imtiaz, M S, Denniss, A, Dos Remedios, C, van Helden, D F, Dulhunty, A F, Laver, D R, Beard, N A
• Format: Journal Article
• Language: English
• Published: England 01.03.2017
• Subjects: Calcium - metabolism; Calcium Signaling; Case-Control Studies; Heart Failure - metabolism; Heart Failure - pathology; Heart Failure - physiopathology; Heart Ventricles - metabolism; Humans; Intracellular Space - metabolism; Magnesium - metabolism; Myocardium - metabolism; Myocytes, Cardiac - metabolism; Phosphorylation; Protein Binding; Protein Processing, Post-Translational; Ryanodine Receptor Calcium Release Channel - metabolism; Sarcoplasmic Reticulum - metabolism; Tacrolimus Binding Proteins - metabolism; Heart failure; Phosphorylation; Mg(2+) and Ca(2+) signalling; Ryanodine receptor; Lipid bilayer; Regulatory proteins
• ISSN: 1095-8584

Heart failure is a multimodal disorder, of which disrupted Ca homeostasis is a hallmark. Central to Ca homeostasis is the major cardiac Ca release channel - the ryanodine receptor (RyR2) - whose activity is influenced by associated proteins, covalent modification and by Ca and Mg . That RyR2 is remodelled and its function disturbed in heart failure is well recognized, but poorly understood. To assess Ca and Mg regulation of RyR2 from left ventricles of healthy, cystic fibrosis and failing hearts, and to correlate these functional changes with RyR2 modifications and remodelling. The function of RyR2 from left ventricular samples was assessed using lipid bilayer single-channel measurements, whilst RyR2 modification and protein:protein interactions were determined using Western Blots and co-immunoprecipitation. In all failing hearts there was an increase in RyR2 activity at end-diastolic cytoplasmic Ca (100nM), a decreased cytoplasmic [Ca ] required for half maximal activation (K ) and a decrease in inhibition by cytoplasmic Mg . This was accompanied by significant hyperphosphorylation of RyR2 S and S , reduced free thiol content and a reduced interaction with FKBP12.0 and FKBP12.6. Either dephosphorylation of RyR2 using PP1 or thiol reduction using DTT eliminated any significant difference in the activity of RyR2 from healthy and failing hearts. We also report a subgroup of RyR2 in failing hearts that were not responsive to regulation by intracellular Ca or Mg . Despite different aetiologies, disrupted RyR2 Ca sensitivity and biochemical modification of the channel are common constituents of failing heart RyR2 and may underlie the pathological disturbances in intracellular Ca signalling.