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- W2344934244 abstract "Loss-of-function mutations in the cytoskeletal protein ankyrin-B (AnkB) cause ventricular tachyarrhythmias in humans. Previously, we found that a larger fraction of the sarcoplasmic reticulum (SR) Ca 2+ leak occurs through Ca 2+ sparks in AnkB-deficient (AnkB +/− ) mice, which may contribute to arrhythmogenicity via Ca 2+ waves. Here, we investigated the mechanisms responsible for increased Ca 2+ spark frequency in AnkB +/− hearts. Using immunoblots and phospho-specific antibodies, we found that phosphorylation of ryanodine receptors (RyRs) by CaMKII is enhanced in AnkB +/− hearts. In contrast, the PKA-mediated RyR phosphorylation was comparable in AnkB +/− and wild-type (WT) mice. CaMKII inhibition greatly reduced Ca 2+ spark frequency in myocytes from AnkB +/− mice but had little effect in the WT. Global activities of the major phosphatases PP1 and PP2A were similar in AnkB +/− and WT hearts, while CaMKII autophosphorylation, a marker of CaMKII activation, was increased in AnkB +/− hearts. Thus, CaMKII-dependent RyR hyperphosphorylation in AnkB +/− hearts is caused by augmented CaMKII activity. Intriguingly, CaMKII activation is limited to the sarcolemma–SR junctions since non-junctional CaMKII targets (phospholamban, HDAC4) are not hyperphosphorylated in AnkB +/− myocytes. This local CaMKII activation may be the consequence of elevated [Ca 2+ ] in the junctional cleft caused by reduced Na + /Ca 2+ exchange activity. Indeed, using the RyR-targeted Ca 2+ sensor GCaMP2.2-FBKP12.6, we found that local junctional [Ca 2+ ] is significantly elevated in AnkB +/− myocytes. The increased incidence of pro-arrhythmogenic Ca 2+ sparks and waves in AnkB +/− hearts is due to enhanced CaMKII-mediated RyR phosphorylation, which is caused by higher junctional [Ca 2+ ] and consequent local CaMKII activation." @default.
- W2344934244 created "2016-06-24" @default.
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- W2344934244 date "2016-04-30" @default.
- W2344934244 modified "2023-10-12" @default.
- W2344934244 title "Elevated local [Ca<sup>2+</sup>] and CaMKII promote spontaneous Ca<sup>2+</sup>release in ankyrin-B-deficient hearts" @default.
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- W2344934244 doi "https://doi.org/10.1093/cvr/cvw093" @default.
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