Journalartikel

Zoxazolamine-induced stimulation of cardiomyogenesis from embryonic stem cells is mediated by Ca2+, nitric oxide and ATP release


AutorenlisteMoehner, Desiree M.; Bernhardt, Anne; Bekhite, Mohamed M.; Schulze, P. Christian; Sauer, Heinrich; Wartenberg, Maria

Jahr der Veröffentlichung2020

ZeitschriftBiochimica et Biophysica Acta (BBA) - Molecular Cell Research

Bandnummer1867

Heftnummer11

ISSN0167-4889

eISSN1879-2596

Open Access StatusBronze

DOI Linkhttps://doi.org/10.1016/j.bbamcr.2020.118796

VerlagElsevier


Abstract
Ca2+-activated potassium (K-Ca) channels of small and intermediate conductance influence proliferation, apoptosis, and cell metabolism. We analysed whether prolonged activation of K(Ca)( )channels by zoxazolamine (ZOX) induces differentiation of mouse embryonic stem (ES) cells towards cardiomyocytes. ZOX treatment of ES cells dose-dependent increased the number and diameter of cardiac foci, the frequency of contractions as well as mRNA expression of the cardiac transcription factor Nkx-2.5, the cardiac markers cardiac troponin I (cTnI), amyosin heavy chain (alpha-MHC), ventricular myosin light chain-2 (MLC2v), and the pacemaker hyperpolarizationactivated, cyclic nucleotide-gated 4 channel (HCN4). ZOX induced hyperpolarization of membrane potential due to activation of IKCa, raised intracellular Ca2+ concentration ([Ca2+](i)) and nitric oxide (NO) in a Ca2+-dependent manner. The Ca2+ response to ZOX was inhibited by chelation of Ca2+ with BAPTA-AM, release of Ca2+ from intracellular stores by thapsigargin and the phospholipase C (PLC) antagonist U73,122. Moreover, the ZOXinduced Ca2+ response was blunted by the purinergic receptor antagonist pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid (PPADS) as well as the specific P2Y(1) antagonist MRS 2,179, suggesting purinergic receptorstimulated signal transduction. Consequently, ZOX initiated ATP release from differentiating ES cells, which was inhibited by the chloride channel inhibitor NPPB and the gap junction inhibitor carbenoxolone (CBX). The stimulation of cardiomyogenesis by ZOX was blunted by the nitric oxide synthase (NOS) inhibitor L-NAME, as well as CBX and NPPB. In summary, our data suggest that ZOX enhances cardiomyogenesis of ES cells by ATP release presumably through gap junctional hemichannels, purinergic receptor activation and intracellular Ca2+ response, thus promoting NO generation.



Zitierstile

Harvard-ZitierstilMoehner, D., Bernhardt, A., Bekhite, M., Schulze, P., Sauer, H. and Wartenberg, M. (2020) Zoxazolamine-induced stimulation of cardiomyogenesis from embryonic stem cells is mediated by Ca2+, nitric oxide and ATP release, Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1867(11), Article 118796. https://doi.org/10.1016/j.bbamcr.2020.118796

APA-ZitierstilMoehner, D., Bernhardt, A., Bekhite, M., Schulze, P., Sauer, H., & Wartenberg, M. (2020). Zoxazolamine-induced stimulation of cardiomyogenesis from embryonic stem cells is mediated by Ca2+, nitric oxide and ATP release. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1867(11), Article 118796. https://doi.org/10.1016/j.bbamcr.2020.118796



Schlagwörter


ACTIVATED POTASSIUM CHANNELSCA2+-ACTIVATED K+ CHANNELSCalcium-activated potassium channelsCARDIOGENESISCardiomyogenesisEmbryonic stem cellsENRICHMENTSMALL-CONDUCTANCETHERAPEUTIC TARGETSZoxazolamine


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