Journalartikel

Stimulation of Cardiomyogenesis of Embryonic Stem Cells by Nitric Oxide Downstream of AMP-Activated Protein Kinase and mTOR Signaling Pathways


AutorenlistePadmasekar, Manju; Sharifpanah, Fatemeh; Finkensieper, Andreas; Wartenberg, Maria; Sauer, Heinrich

Jahr der Veröffentlichung2011

Seiten2163-2175

ZeitschriftStem Cells and Development

Bandnummer20

Heftnummer12

ISSN1547-3287

DOI Linkhttps://doi.org/10.1089/scd.2010.0581

VerlagMary Ann Liebert


Abstract
Nitric oxide (NO) is a key regulator of cardiomyogenesis of embryonic stem (ES) cells. However, signaling pathways involving the energy sensor AMP-activated protein kinase (AMPK) and/or mammalian target of rapamycin (mTOR) resulting in NO generation and stimulation of cardiomyogenesis are currently not known. Herein, the role of AMPK-versus mTOR-regulated signaling pathways and the impact of NO for cardiomyogenesis of mouse ES cells were investigated. Activation of AMPK by 5-amino-4-imidazolecarboxamide riboside (AICAr) or metformin as well as inactivation of AMPK by compound C (Comp C), siRNA ablation of AMPK alpha 2, or exogenous ATP stimulated cardiomyogenesis of ES cells. Inhibition of AMPK by Comp C resulted in phosphorylation of mTOR and generation of NO. NO generation was likewise achieved when AMPK was either activated by AICAr or mTOR was inhibited by rapamycin, suggesting that NO generation occurred by two mutually active parallel signaling pathways, one being AMPK dependent and mTOR independent (AICAr pathway) and the other being AMPK independent and mTOR dependent (Comp C pathway). Consequently, cardiomyogenesis as well as NO generation was completely abrogated when ES cells were cultivated in the presence of rapamycin and Comp C, which inhibit both signaling pathways. The impact of NO for cardiomyogenesis of ES cells was corroborated in experiments showing that the effects of Comp C on cardiomyogenesis of ES cells were abolished by the NO synthase inhibitors NG-monomethyl-L-arginine and N (G)-nitro-L-arginine methyl ester. In summary, our data demonstrate that NO generation downstream of AMPK and mTOR is activated by distinct, interacting signaling pathways that initiate cardiomyogenesis of ES cells.



Zitierstile

Harvard-ZitierstilPadmasekar, M., Sharifpanah, F., Finkensieper, A., Wartenberg, M. and Sauer, H. (2011) Stimulation of Cardiomyogenesis of Embryonic Stem Cells by Nitric Oxide Downstream of AMP-Activated Protein Kinase and mTOR Signaling Pathways, Stem Cells and Development, 20(12), pp. 2163-2175. https://doi.org/10.1089/scd.2010.0581

APA-ZitierstilPadmasekar, M., Sharifpanah, F., Finkensieper, A., Wartenberg, M., & Sauer, H. (2011). Stimulation of Cardiomyogenesis of Embryonic Stem Cells by Nitric Oxide Downstream of AMP-Activated Protein Kinase and mTOR Signaling Pathways. Stem Cells and Development. 20(12), 2163-2175. https://doi.org/10.1089/scd.2010.0581



Schlagwörter


Cardiomyocyte differentiationES CELLSNADPH OXIDASESYNTHASE


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