Key result
Ankyrin-B dysfunction is associated with significant electrical and structural cardiac phenotypes, including sinus node dysfunction, atrial fibrillation, and sudden cardiac death.
Why the study?
Ankyrin-B plays critical roles in cardiac physiology, and its dysfunction leads to diverse electrical, structural, and arrhythmogenic phenotypes in animal models and humans.
This review highlights the critical role of ankyrin-B in cardiac ion channel localization and its association with life-threatening arrhythmias and structural remodeling.
Ankyrin-B dysfunction may warrant inclusion in arrhythmia genetic panels; leaves open prospective validation and therapeutic targeting.
), originally identified as a key cytoskeletal-associated protein in the brain, is highly expressed in the heart and plays critical roles in cardiac physiology and cell biology. In the heart, ankyrin-B plays key roles in the targeting and localization of key ion channels and transporters, structural proteins, and signaling molecules. The role of ankyrin-B in normal cardiac function is illustrated in animal models lacking ankyrin-B expression, which display significant electrical and structural phenotypes and life-threatening arrhythmias. Further, ankyrin-B dysfunction has been associated with cardiac phenotypes in humans (now referred to as "ankyrin-B syndrome") including sinus node dysfunction, heart rate variability, atrial fibrillation, conduction block, arrhythmogenic cardiomyopathy, structural remodeling, and sudden cardiac death. Here, we review the diverse roles of ankyrin-B in the vertebrate heart with a significant focus on ankyrin-B-linked cell- and molecular-pathways and disease.
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Sucharski et al. (2020) conducted a review in Ankyrin-B syndrome and cardiac arrhythmias. Ankyrin-B dysfunction was evaluated. Ankyrin-B dysfunction is associated with significant electrical and structural cardiac phenotypes, including sinus node dysfunction, atrial fibrillation, and sudden cardiac death.
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