Popeye domain containing proteins modulate the voltage-gated cardiac sodium channel Nav1.5

被引:0
|
作者
Rinne, Susanne [1 ]
Kiper, Aytug K. [1 ]
Jacob, Ralf [2 ]
Ortiz-Bonnin, Beatriz [1 ]
Schindler, Roland F. R. [3 ,10 ]
Fischer, Sabine [4 ]
Komadowski, Marlene [1 ]
De Martino, Emilia [1 ]
Schaefer, Martin K. -H. [5 ]
Cornelius, Tamina [1 ]
Fabritz, Larissa [6 ,7 ,8 ,9 ]
Helker, Christian S. M. [4 ]
Brand, Thomas [3 ]
Decher, Niels [1 ]
机构
[1] Philipps Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, Germany
[2] Philipps Univ Marburg, Inst Cytobiol, Ctr Synthet Microbiol, D-35043 Marburg, Germany
[3] Imperial Coll London, Natl Lung & Heart Inst, Du Cane Rd, London W12 0NN, England
[4] Philipps Univ Marburg, Fac Biol Cell Signaling & Dynam, D-35043 Marburg, Germany
[5] Philipps Univ Marburg, Inst Anat & Cell Biol, D-35037 Marburg, Germany
[6] Univ Birmingham, Inst Cardiovasc Sci, Birmingham B15 2TT, England
[7] Univ Med Ctr Hamburg Eppendorf, Univ Ctr Cardiovasc Sci, Univ Heart & Vasc Ctr Hamburg, D-20251 Hamburg, Germany
[8] Univ Med Ctr Hamburg Eppendorf, Univ Heart & Vasc Ctr Hamburg, Dept Cardiol, D-20251 Hamburg, Germany
[9] DZHK Hamburg Kiel Lubeck, Hamburg, Germany
[10] Domainex Ltd, Chesterford Res Pk, Saffron Walden CB10 1XL, England
关键词
STRESS-MEDIATED MODULATION; LONG-QT; MOLECULAR-MECHANISM; SKELETAL-MUSCLE; GENE; MUTATIONS; SCN5A; ATRIAL; BVES; ARRHYTHMIA;
D O I
10.1016/j.isci.2024.109696
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 POPDC2modulated 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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页数:15
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