PUBLICATION
            Popeye domain containing proteins modulate the voltage-gated cardiac sodium channel Nav1.5
- Authors
 - Rinné, S., Kiper, A.K., Jacob, R., Ortiz-Bonnin, B., Schindler, R.F.R., Fischer, S., Komadowski, M., De Martino, E., Schäfer, M.K., Cornelius, T., Fabritz, L., Helker, C.S.M., Brand, T., Decher, N.
 - ID
 - ZDB-PUB-240501-4
 - Date
 - 2024
 - Source
 - iScience 27: 109696109696 (Journal)
 - Registered Authors
 - Brand, Thomas, Fischer, Sabine, Helker, Christian
 - Keywords
 - Biochemistry, Molecular biology, Physiology
 - MeSH Terms
 - none
 - PubMed
 - 38689644 Full text @ iScience
 
            Citation
        
        
            Rinné, S., Kiper, A.K., Jacob, R., Ortiz-Bonnin, B., Schindler, R.F.R., Fischer, S., Komadowski, M., De Martino, E., Schäfer, M.K., Cornelius, T., Fabritz, L., Helker, C.S.M., Brand, T., Decher, N. (2024) Popeye domain containing proteins modulate the voltage-gated cardiac sodium channel Nav1.5. iScience. 27:109696109696.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Popeye domain containing (POPDC) proteins are predominantly expressed in the heart and skeletal muscle, modulating the K2P potassium channel TREK-1 in a cAMP-dependent manner. POPDC1 and POPDC2 variants cause cardiac conduction disorders with or without muscular dystrophy. Searching for POPDC2-modulated ion channels using a functional co-expression screen in Xenopus oocytes, we found POPDC proteins to modulate the cardiac sodium channel Nav1.5. POPDC proteins downregulate Nav1.5 currents in a cAMP-dependent manner by reducing the surface expression of the channel. POPDC2 and Nav1.5 are both expressed in different regions of the murine heart and consistently POPDC2 co-immunoprecipitates with Nav1.5 from native cardiac tissue. Strikingly, the knock-down of popdc2 in embryonic zebrafish caused an increased upstroke velocity and overshoot of cardiac action potentials. The POPDC modulation of Nav1.5 provides a new mechanism to regulate cardiac sodium channel densities under sympathetic stimulation, which is likely to have a functional impact on cardiac physiology and inherited arrhythmias.
            
    
        
        
    
    
    
                
                    
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