Journalartikel

VEGF-mediated PI3K class IA and PKC signaling in cardiomyogenesis and vasculogenesis of mouse embryonic stem cells


AutorenlisteBekhite, Mohamed M.; Finkensieper, Andreas; Binas, Stephanie; Mueller, Joerg; Wetzker, Reinhard; Figulla, Hans-Reiner; Sauer, Heinrich; Wartenberg, Maria

Jahr der Veröffentlichung2011

Seiten1819-1830

ZeitschriftJournal of Cell Science

Bandnummer124

Heftnummer11

ISSN0021-9533

eISSN1477-9137

DOI Linkhttps://doi.org/10.1242/jcs.077594

VerlagThe Company of Biologists


Abstract
VEGF-, phosphoinositide 3-kinase (PI3K)- and protein kinase C (PKC)-regulated signaling in cardiac and vascular differentiation was investigated in mouse ES cells and in ES cell-derived Flk-1(+) cardiovascular progenitor cells. Inhibition of PI3K by wortmannin and LY294002, disruption of PI3K catalytic subunits p110 alpha and p110 delta using short hairpin RNA (shRNA), or inhibition of p110 alpha with compound 15e and of p110 delta with IC-87114 impaired cardiac and vascular differentiation. By contrast, TGX-221, an inhibitor of p110 beta, and shRNA knockdown of p110 beta were without significant effects. Antagonists of the PKC family, i.e. bisindolylmaleimide-1 (BIM-1), G 6976 (targeting PKC alpha/beta II) and rottlerin (targeting PKC delta) abolished vasculogenesis, but not cardiomyogenesis. Inhibition of Akt blunted cardiac as well as vascular differentiation. VEGF induced phosphorylation of PKC alpha/beta II and PKC delta but not PKC zeta. This was abolished by PI3K inhibitors and the VEGFR-2 antagonist SU5614. Furthermore, phosphorylation of Akt and phosphoinositide-dependent kinase-1 (PDK1) was blunted upon inhibition of PI3K, but not upon inhibition of PKC by BIM-1, suggesting that activation of Akt and PDK1 by VEGF required PI3K but not PKC. In summary, we demonstrate that PI3K catalytic subunits p110 alpha and p110 delta are central to cardiovasculogenesis of ES cells. Akt downstream of PI3K is involved in both cardiomyogenesis and vasculogenesis, whereas PKC is involved only in vasculogenesis.



Zitierstile

Harvard-ZitierstilBekhite, M., Finkensieper, A., Binas, S., Mueller, J., Wetzker, R., Figulla, H., et al. (2011) VEGF-mediated PI3K class IA and PKC signaling in cardiomyogenesis and vasculogenesis of mouse embryonic stem cells, Journal of Cell Science, 124(11), pp. 1819-1830. https://doi.org/10.1242/jcs.077594

APA-ZitierstilBekhite, M., Finkensieper, A., Binas, S., Mueller, J., Wetzker, R., Figulla, H., Sauer, H., & Wartenberg, M. (2011). VEGF-mediated PI3K class IA and PKC signaling in cardiomyogenesis and vasculogenesis of mouse embryonic stem cells. Journal of Cell Science. 124(11), 1819-1830. https://doi.org/10.1242/jcs.077594



Schlagwörter


AktCARDIOMYOCYTES IN-VITROCardiovascular differentiationCARDIOVASCULAR PROGENITOR CELLSEmbryonic stem cellsENDOTHELIAL GROWTH-FACTORHEART SIZEPHOSPHATIDYLINOSITOL 3-KINASEPhosphoinositide 3-kinasePHOSPHOINOSITIDE 3-KINASE PATHWAYProtein kinase CPROTEIN-KINASE-C


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