1. AKAP18δ Anchors and Regulates CaMKII Activity at Phospholamban-SERCA2 and RYR
- Author
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William E. Louch, Geir Christensen, Pimthanya Wanichawan, Hilde Jarstadmarken, Enno Klussmann, Marie C. Moutty, Ivar Sjaastad, Viacheslav O. Nikolaev, Cathrine R. Carlson, Per Kristian Lunde, Laetitia Pereira, Anna Bergan-Dahl, Ole M. Sejersted, Jan Magnus Aronsen, Marianne Lunde, Terje R Selnes Kolstad, Susanne Hille, Donald M. Bers, Bjørn Dalhus, Hariharan Subramanian, Oliver Müller, and Xin Shen
- Subjects
calmodulin ,Calmodulin ,cardiac ,Physiology ,Cells ,Clinical Sciences ,Wistar ,Cardiorespiratory Medicine and Haematology ,Sarcoplasmic Reticulum Calcium-Transporting ATPases ,Ca2+/calmodulin-dependent protein kinase ,ryanodine receptor ,Animals ,Humans ,Myocytes, Cardiac ,Calcium Signaling ,Rats, Wistar ,Cells, Cultured ,phospholamban ,Adaptor Proteins, Signal Transducing ,Myocytes ,Cultured ,Binding Sites ,biology ,Chemistry ,Activator (genetics) ,Kinase ,Ryanodine receptor ,Endoplasmic reticulum ,Calcium-Binding Proteins ,Signal Transducing ,Adaptor Proteins ,Ryanodine Receptor Calcium Release Channel ,calcium-calmodulin-dependent protein kinase type 2 ,musculoskeletal system ,Rats ,Phospholamban ,Cell biology ,HEK293 Cells ,Cardiovascular System & Hematology ,Cardiovascular and Metabolic Diseases ,cardiovascular system ,biology.protein ,Phosphorylation ,Calcium-Calmodulin-Dependent Protein Kinase Type 2 ,Cardiology and Cardiovascular Medicine ,Protein Binding - Abstract
Background: The sarcoplasmic reticulum (SR) Ca 2+ -ATPase 2 (SERCA2) mediates Ca 2+ reuptake into SR and thereby promotes cardiomyocyte relaxation, whereas the ryanodine receptor (RYR) mediates Ca 2+ release from SR and triggers contraction. Ca 2+ /CaMKII (CaM [calmodulin]-dependent protein kinase II) regulates activities of SERCA2 through phosphorylation of PLN (phospholamban) and RYR through direct phosphorylation. However, the mechanisms for CaMKIIδ anchoring to SERCA2-PLN and RYR and its regulation by local Ca 2+ signals remain elusive. The objective of this study was to investigate CaMKIIδ anchoring and regulation at SERCA2-PLN and RYR. Methods: A role for AKAP18δ (A-kinase anchoring protein 18δ) in CaMKIIδ anchoring and regulation was analyzed by bioinformatics, peptide arrays, cell-permeant peptide technology, immunoprecipitations, pull downs, transfections, immunoblotting, proximity ligation, FRET-based CaMKII activity and ELISA-based assays, whole cell and SR vesicle fluorescence imaging, high-resolution microscopy, adenovirus transduction, adenoassociated virus injection, structural modeling, surface plasmon resonance, and alpha screen technology. Results: Our results show that AKAP18δ anchors and directly regulates CaMKIIδ activity at SERCA2-PLN and RYR, via 2 distinct AKAP18δ regions. An N-terminal region (AKAP18δ-N) inhibited CaMKIIδ through binding of a region homologous to the natural CaMKII inhibitor peptide and the Thr17-PLN region. AKAP18δ-N also bound CaM, introducing a second level of control. Conversely, AKAP18δ-C, which shares homology to neuronal CaMKIIα activator peptide (N2B-s), activated CaMKIIδ by lowering the apparent Ca 2+ threshold for kinase activation and inducing CaM trapping. While AKAP18δ-C facilitated faster Ca 2+ reuptake by SERCA2 and Ca 2+ release through RYR, AKAP18δ-N had opposite effects. We propose a model where the 2 unique AKAP18δ regions fine-tune Ca 2+ -frequency-dependent activation of CaMKIIδ at SERCA2-PLN and RYR. Conclusions: AKAP18δ anchors and functionally regulates CaMKII activity at PLN-SERCA2 and RYR, indicating a crucial role of AKAP18δ in regulation of the heartbeat. To our knowledge, this is the first protein shown to enhance CaMKII activity in heart and also the first AKAP (A-kinase anchoring protein) reported to anchor a CaMKII isoform, defining AKAP18δ also as a CaM-KAP.
- Published
- 2022
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