Dysfunction in the βII Spectrin-Dependent Cytoskeleton Underlies Human Arrhythmia
| Autor: | Ingrid M. Bonilla, Ahmet Kilic, Thomas J. Hund, Iuliia Polina, Amy C. Sturm, Raul Weiss, Langston D. Hughes, Robert S.D. Higgins, Crystal F. Kline, Victor P. Long, Mingzhai Sun, Philip F. Binkley, Tyler R. Webb, Patrick Wright, Peter J. Mohler, Matthew N. Rasband, Dobromir Dobrev, Jerry Curran, Matteo Vatta, Zhiyi Wei, Niels Voigt, Cynthia A. Carnes, Michael A. Makara, Deepak Bhakta, Mingjie Zhang, Chuansheng Zhang, Paul M. Janssen, Katherine G. Spoonamore, Sakima A. Smith, Sean C. Little, Jianjie Ma |
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| Jazyk: | angličtina |
| Rok vydání: | 2015 |
| Předmět: |
medicine.medical_specialty
Medizin Biology Article Physiology (medical) Internal medicine medicine Myocyte Ankyrin Animals Humans Spectrin Myocytes Cardiac Cytoskeleton chemistry.chemical_classification Cardiac arrhythmia Arrhythmias Cardiac Microfilament Protein Transport protein Cell biology Endocrinology Membrane protein chemistry Cardiology and Cardiovascular Medicine |
| Popis: | Background— The cardiac cytoskeleton plays key roles in maintaining myocyte structural integrity in health and disease. In fact, human mutations in cardiac cytoskeletal elements are tightly linked to cardiac pathologies, including myopathies, aortopathies, and dystrophies. Conversely, the link between cytoskeletal protein dysfunction and cardiac electric activity is not well understood and often overlooked in the cardiac arrhythmia field. Methods and Results— Here, we uncover a new mechanism for the regulation of cardiac membrane excitability. We report that βII spectrin, an actin-associated molecule, is essential for the posttranslational targeting and localization of critical membrane proteins in heart. βII spectrin recruits ankyrin-B to the cardiac dyad, and a novel human mutation in the ankyrin-B gene disrupts the ankyrin-B/βII spectrin interaction, leading to severe human arrhythmia phenotypes. Mice lacking cardiac βII spectrin display lethal arrhythmias, aberrant electric and calcium handling phenotypes, and abnormal expression/localization of cardiac membrane proteins. Mechanistically, βII spectrin regulates the localization of cytoskeletal and plasma membrane/sarcoplasmic reticulum protein complexes, including the Na/Ca exchanger, ryanodine receptor 2, ankyrin-B, actin, and αII spectrin. Finally, we observe accelerated heart failure phenotypes in βII spectrin–deficient mice. Conclusions— Our findings identify βII spectrin as critical for normal myocyte electric activity, link this molecule to human disease, and provide new insight into the mechanisms underlying cardiac myocyte biology. |
| Databáze: | OpenAIRE |
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