دورية أكاديمية
Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic Cardiomyopathy
| العنوان: | Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic Cardiomyopathy |
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| المؤلفون: | Toepfer, C.N. (Christopher N.), Garfinkel, A.C. (Amanda C.), Venturini, G. (Gabriela), Wakimoto, H. (Hiroko), Repetti, G. (Giuliana), Alamo, L. (Lorenzo), Sharma, A. (Arun), Agarwal, R. (Radhika), Ewoldt, J.F. (Jourdan F.), Cloonan, P. (Paige), Letendre, J. (Justin), Lun, M. (Mingyue), Olivotto, I. (Iacopo), Colan, S.D. (Steven), Ashley, E. (Euan), Jacoby, D. (Daniel), Michels, M. (Michelle), Redwood, C. (Charles), Watkins, H.C. (Hugh C.), Day, S.M. (Sharlene M.), Staples, J.F. (James F.), Padrón, R. (Raúl), Chopra, A. (Anant), Ho, C.Y. (Carolyn Y.), Chen, C.S. (Christopher S.), Pereira, A. (A.), Seidman, J.G. (Jonathan G.), Seidman, C. (Christine) |
| المصدر: | Circulation (Baltimore) vol. 141 no. 10, pp. 828-842 |
| سنة النشر: | 2020 |
| المجموعة: | RePub - Publications from Erasmus University, Rotterdam |
| مصطلحات موضوعية: | cardiomyopathy, hypertrophic, cardiovascular physiological phenomena, myosins, sarcomeres |
| الوصف: | BACKGROUND: Hypertrophic cardiomyopathy (HCM) is caused by pathogenic variants in sarcomere protein genes that evoke hypercontractility, poor relaxation, and increased energy consumption by the heart and increased patient risks for arrhythmias and heart failure. Recent studies show that pathogenic missense variants in myosin, the molecular motor of the sarcomere, are clustered in residues that participate in dynamic conformational states of sarcomere proteins. We hypothesized that these conformations are essential to adapt contractile output for energy conservation and that pathophysiology of HCM results from destabilization of these conformations. METHODS: We assayed myosin ATP binding to define the proportion of myosins in the super relaxed state (SRX) conformation or the disordered relaxed state (DRX) conformation in healthy rodent and human hearts, at baseline and in response to reduced hemodynamic demands of hibernation or pathogenic HCM variants. To determine the relationships between myosin conformations, sarcomere function, and cell biology, we assessed contractility, relaxation, and cardiomyocyte morphology and metabolism, with and without an allosteric modulator of myosin ATPase activity. We then tested whether the positions of myosin variants of unknown clinical significance that were identified in patients with HCM, predicted functional consequences and associations with heart failure and arrhythmias. RESULTS: Myosins undergo physiological shifts between the SRX conformation that maximizes energy conservation and the DRX conformation that enables cross-bridge formation with greater ATP consumption. Systemic hemodynamic requirements, pharmacological modulators of myosin, and pathogenic myosin missense mutations influenced the proportions of these conformations. Hibernation increased the proportion of myosins in the SRX conformation, whereas pathogenic variants destabilized these and increased the proportion of myosins in the DRX conformation, which enhanced cardiomyocyte contractility, but impaired ... |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English |
| العلاقة: | http://repub.eur.nl/pub/125649Test; urn:hdl:1765/125649 |
| DOI: | 10.1161/CIRCULATIONAHA.119.042339 |
| الإتاحة: | https://doi.org/10.1161/CIRCULATIONAHA.119.042339Test http://repub.eur.nl/pub/125649Test |
| حقوق: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.C480945 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1161/CIRCULATIONAHA.119.042339 |
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