Journal article

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


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

Publication year2007

Pages568-574

JournalCardiovascular Research

Volume number73

Issue number3

ISSN0008-6363

eISSN1755-3245

Open access statusBronze

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

PublisherOxford 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.




Citation Styles

Harvard Citation styleAbdallah, 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 Citation styleAbdallah, 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



Keywords


ADP-RIBOSEendothelial cellPARPproloferationTRPM2

Last updated on 2025-10-06 at 09:40