1. Activation of histone deacetylase-6 induces contractile dysfunction through derailment of α-tubulin proteostasis in experimental and human atrial fibrillation
- Author
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Akar Ar, Roelien A. M. Meijering, Chia-Tung Wu, Deli Zhang, Xiao-Yan Qi, Robert H. Henning, Bianca J. J. M. Brundel, Artavazd Tadevosyan, Ody C. M. Sibon, Serkan Durdu, Femke Hoogstra-Berends, Gunseli Cubukcuoglu Deniz, Stanley Nattel, Molecular Neuroscience and Ageing Research (MOLAR), Cardiovascular Centre (CVC), Vascular Ageing Programme (VAP), Groningen Kidney Center (GKC), Groningen Institute for Organ Transplantation (GIOT), and Physiology
- Subjects
Indoles ,CYTOSKELETON ,Histone Deacetylase 6 ,Hydroxamic Acids ,Microtubules ,DISEASE ,THERAPEUTIC TARGETS ,Mice ,Tubulin ,Drosophila Proteins ,Myocytes, Cardiac ,atrial fibrillation ,biology ,Calpain ,Cardiac Pacing, Artificial ,HDAC6 protein ,Cell biology ,Histone ,HEART ,Drosophila ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,Alpha-tubulin deacetylase ,Human ,Deacetylase activity ,medicine.medical_specialty ,ACETYLATION ,alpha-tubulin deacetylase ,HDAC6 INHIBITOR ,Histone Deacetylases ,Dogs ,Genetic ,MICROTUBULE DISRUPTION ,Physiology (medical) ,Internal medicine ,medicine ,Animals ,Humans ,Epigenetics ,human ,PROTEOLYSIS ,Fibrillation ,epigenesis ,Atrial Remodeling ,HDAC6 ,DEGRADATION ,Myocardial Contraction ,Atrial fibrillation ,Endocrinology ,Proteostasis ,Acetylation ,biology.protein ,genetic ,STRUCTURAL-CHANGES ,HeLa Cells ,Epigenesis - Abstract
Background— Atrial fibrillation (AF) is characterized by structural remodeling, contractile dysfunction, and AF progression. Histone deacetylases (HDACs) influence acetylation of both histones and cytosolic proteins, thereby mediating epigenetic regulation and influencing cell proteostasis. Because the exact function of HDACs in AF is unknown, we investigated their role in experimental and clinical AF models. Methods and Results— Tachypacing of HL-1 atrial cardiomyocytes and Drosophila pupae hearts significantly impaired contractile function (amplitude of Ca 2+ transients and heart wall contractions). This dysfunction was prevented by inhibition of HDAC6 (tubacin) and sirtuins (nicotinamide). Tachypacing induced specific activation of HDAC6, resulting in α-tubulin deacetylation, depolymerization, and degradation by calpain. Tachypacing-induced contractile dysfunction was completely rescued by dominant-negative HDAC6 mutants with loss of deacetylase activity in the second catalytic domain, which bears α-tubulin deacetylase activity. Furthermore, in vivo treatment with the HDAC6 inhibitor tubastatin A protected atrial tachypaced dogs from electric remodeling (action potential duration shortening, L-type Ca 2+ current reduction, AF promotion) and cellular Ca 2+ -handling/contractile dysfunction (loss of Ca 2+ transient amplitude, sarcomere contractility). Finally, atrial tissue from patients with AF also showed a significant increase in HDAC6 activity and reduction in the expression of both acetylated and total α-tubulin. Conclusions— AF induces remodeling and loss of contractile function, at least in part through HDAC6 activation and subsequent derailment of α-tubulin proteostasis and disruption of the cardiomyocyte microtubule structure. In vivo inhibition of HDAC6 protects against AF-related atrial remodeling, disclosing the potential of HDAC6 as a therapeutic target in clinical AF.
- Published
- 2014
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