Journalartikel

The role of poly(ADP-ribose) polymerase (PARP) in the autonomous proliferative response of endothelial cells to hypoxia


AutorenlisteAbdallah, Yaser; Gligorievski, Dragan; Kasseckert, Sascha A.; Dieterich, Lukas; Schaefer, Matthias; Kuhlmann, Christoph R.; Noll, Thomas; Sauer, Heinrich; Piper, H. Michael; Schaefer, Claudia

Jahr der Veröffentlichung2007

Seiten568-574

ZeitschriftCardiovascular Research

Bandnummer73

Heftnummer3

ISSN0008-6363

eISSN1755-3245

Open Access StatusBronze

DOI Linkhttps://doi.org/10.1016/j.cardiores.2006.11.027

VerlagOxford University Press


Abstract

Objective: The autonomous proliferative response of endothelial cells to hypoxia has been shown to be dependent on activation of NAD(P)H oxidase, on the cytosolic Ca2+ load, and, consequently, on nuclear translocation of extracellular signal-regulated kinase (ERK)1/2 during transient hypoxia. The aim of the present study was to investigate whether poly(ADP-ribose) polymerase (PARP) is a downstream signal of NAD(P)H oxidase, mediating cytosolic Ca2+ load and hence nuclear translocation of ERK1/2 and endothelial cell proliferation.

Methods: Porcine aortic endothelial cells were incubated under hypoxic conditions for 40 min. Cytosolic [Ca2+] and reactive oxygen species (ROS) formation were measured in fura-2- and DCF-loaded cells, respectively. PARP activation was detected by immunocytochemistry, and endothelial cell proliferation was determined 24 h after 60 min of transient hypoxia.

Results: Inhibition of NAD(P)H oxidase with antisense oligonucleotide against the p22(phox) subunit, MEK/ERK signalling with UO 126 (30 mu M), or PARP with PJ 34 (10 mu M) leads to a marked reduction in hypoxia-induced cytosolic Ca2+ load and activation of PARP. Hypoxia-induced translocation of ERKI/2 and endothelial cell proliferation were also prevented when NAD(P)H oxidase or PARP were inhibited; however, hypoxic ROS formation was not affected in the presence of PARP inhibitor.

Conclusion: PARP represents a downstream effector of NADP(H) oxidase and acts as a necessary intermediate step for the hypoxic proliferative response of endothelial cells. (c) 2006 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.




Zitierstile

Harvard-ZitierstilAbdallah, Y., Gligorievski, D., Kasseckert, S., Dieterich, L., Schaefer, M., Kuhlmann, C., et al. (2007) The role of poly(ADP-ribose) polymerase (PARP) in the autonomous proliferative response of endothelial cells to hypoxia, Cardiovascular Research, 73(3), pp. 568-574. https://doi.org/10.1016/j.cardiores.2006.11.027

APA-ZitierstilAbdallah, Y., Gligorievski, D., Kasseckert, S., Dieterich, L., Schaefer, M., Kuhlmann, C., Noll, T., Sauer, H., Piper, H., & Schaefer, C. (2007). The role of poly(ADP-ribose) polymerase (PARP) in the autonomous proliferative response of endothelial cells to hypoxia. Cardiovascular Research. 73(3), 568-574. https://doi.org/10.1016/j.cardiores.2006.11.027



Schlagwörter


ADP-RIBOSEendothelial cellPARPproloferationTRPM2


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