Piezo1 and BKCa channels in human atrial fibroblasts: Interplay and remodelling in atrial fibrillation
Autor: | Eva A. Rog-Zielinska, Elisa Darkow, Susanne Proksch, Matthias Karck, Dorothee Jakob, Peter Kohl, Fabian A. Kari, Constanze Schmidt, Alexander Klesen, Ramona Emig, Tim Guth, Hélène Guizouarn, Stephan R Künzel, Diana Aria, Benoit Allegrini, Rémi Peyronnet, Ana Simon Chica, Friedhelm Beyersdorf, Stéphane N. Hatem, Ursula Ravens |
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Přispěvatelé: | University of Freiburg [Freiburg], Institut de Biologie Valrose (IBV), Université Nice Sophia Antipolis (1965 - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA), Unité de Recherche sur les Maladies Cardiovasculaires, du Métabolisme et de la Nutrition = Research Unit on Cardiovascular and Metabolic Diseases (ICAN), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Institut de Cardiométabolisme et Nutrition = Institute of Cardiometabolism and Nutrition [CHU Pitié Salpêtrière] (IHU ICAN), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Heidelberg University, Technische Universität Dresden = Dresden University of Technology (TU Dresden), Azevedo, Chloe |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
[SDV]Life Sciences [q-bio] Non-myocytes 030204 cardiovascular system & hematology 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine KCNMA1 medicine Sinus rhythm Paxilline Mechano-sensing Molecular Biology Ion channel PIEZO1 Heart Atrial fibrillation Iberiotoxin medicine.disease Potassium channel Cell biology [SDV] Life Sciences [q-bio] Electrophysiology 030104 developmental biology chemistry Stretch-activated ion channels Calcium Cardiology and Cardiovascular Medicine Arrhythmia |
Zdroj: | Journal of Molecular and Cellular Cardiology Journal of Molecular and Cellular Cardiology, 2021, 158, pp.49-62. ⟨10.1016/j.yjmcc.2021.05.002⟩ |
ISSN: | 0022-2828 1095-8584 |
Popis: | International audience; Aims: Atrial Fibrillation (AF) is an arrhythmia of increasing prevalence in the aging populations of developed countries. One of the important indicators of AF is sustained atrial dilatation, highlighting the importance of mechanical overload in the pathophysiology of AF. The mechanisms by which atrial cells, including fibroblasts, sense and react to changing mechanical forces, are not fully elucidated. Here, we characterise stretch-activated ion channels (SAC) in human atrial fibroblasts and changes in SAC- presence and activity associated with AF.Methods and results: Using primary cultures of human atrial fibroblasts, isolated from patients in sinus rhythm or sustained AF, we combine electrophysiological, molecular and pharmacological tools to identify SAC. Two electrophysiological SAC- signatures were detected, indicative of cation-nonselective and potassium-selective channels. Using siRNA-mediated knockdown, we identified the cation-nonselective SAC as Piezo1. Biophysical properties of the potassium-selective channel, its sensitivity to calcium, paxilline or iberiotoxin (blockers), and NS11021 (activator), indicated presence of calcium-dependent 'big potassium channels' (BKCa). In cells from AF patients, Piezo1 activity and mRNA expression levels were higher than in cells from sinus rhythm patients, while BKCa activity (but not expression) was downregulated. Both Piezo1-knockdown and removal of extracellular calcium from the patch pipette resulted in a significant reduction of BKCa current during stretch. No co-immunoprecipitation of Piezo1 and BKCa was detected.Conclusions: Human atrial fibroblasts contain at least two types of ion channels that are activated during stretch: Piezo1 and BKCa. While Piezo1 is directly stretch-activated, the increase in BKCa activity during mechanical stimulation appears to be mainly secondary to calcium influx via SAC such as Piezo1. During sustained AF, Piezo1 is increased, while BKCa activity is reduced, highlighting differential regulation of both channels. Our data support the presence and interplay of Piezo1 and BKCa in human atrial fibroblasts in the absence of physical links between the two channel proteins. |
Databáze: | OpenAIRE |
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