Meet Inspiring Speakers and Experts at our 3000+ Global Conference Series LLC LTD Events with over 1000+ Conferences, 1000+ Symposiums
and 1000+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business.

Explore and learn more about Conference Series LLC LTD : World’s leading Event Organizer


3rd Global Summit on Heart Diseases

Bangkok, Thailand

Janos Magyar

Janos Magyar

University of Debrecen, Hungary

Title: Chloride current in mammalian ventricular cells


Biography: Janos Magyar


Background: Calcium activated Cl current (ICl(Ca)) mediated by TMEM16A and/or Bestrophin-3 may contribute to cardiac arrhythmias. Our goal was to study the ICl(Ca) profile during an actual ventricular action potential (AP) under normal calcium cycling as well as in case of altered intracellular calcium concentration ([Ca2+]i). The expression of TMEM16A and/or Bestrophin-3 in canine and human left ventricular myocytes was examined.

Methods: Whole-cell configuration of the patch-clamp technique and action potential voltage-clamp were used to monitor ICl(Ca), detected as 9‑anthracene carboxylic acid (9‑AC)-sensitive current. FURA-2-AM dye was used to measure [Ca2+]i. Expression and cellular localization of Cav1.2, Bestrophin-3 and TMEM16A was analyzed with immunocytochemistry and confocal microscopy.

Results: Under AP voltage-clamp conditions the profile of ICl(Ca) contained an early fast outward (1.62±0.06 A/F) and a late inward component (-0.16±0.02 A/F). Both components were reduced by ryanodine (1.05±0.03 A/F; -0.07±0.03 A/F), while fully abolished by BAPTA, but not EGTA (1.17±0.09 A/F; −0.13±0.02 A/F). Setting [Ca2+]i to 1.1 µM decreased ICl(Ca), while application of Bay K8644, isoproterenol increased the amplitude of ICl(Ca). Both L-type Ca2+ current and ICl(Ca) were eliminated by nisoldipine. TMEM16A and Bestrophin-3 showed strong co-localization with one another and also with Cav1.2 channels both canine myocytes and human ventricular myocardium.

Conclusions: Activation of ICl(Ca) in canine ventricular cells requires calcium entry through neighboring L-type Ca2+ channels and is only augmented by SR Ca2+-release. Substantial activation of ICl(Ca) requires high Ca2+ in the dyadic clefts which can be effectively buffered by BAPTA, but not EGTA.