The Role of PARP Activation in Glutamate-Induced Necroptosis in HT-22 Cells
Document Type
Article
Publication Date
7-9-2010
Description
Oxidative cell death contributes to neuronal cell death in many neurological diseases such as stroke, brain trauma, and Alzheimer's disease. In this study, we explored the involvement of poly(ADP-ribose)-polymerase (PARP) in oxidative stress-induced necroptosis. We showed that PJ34, a potent and specific inhibitor of PARP, can completely inhibit glutamate-induced necroptosis in HT-22 cells. This protective effect was still observed 8 h after glutamate exposure followed by PJ34 treatment. These results suggest that PARP activation plays a critical role in glutamate-induced necroptosis. We also examined the interaction between PARP and a necroptosis inhibitor called necrostatin-1 (Nec-1). Previously, we showed that Nec-1 protects against glutamate-induced oxytosis by inhibiting the translocation of cellular apoptosis-inducing factor (AIF), a downstream target of PARP-1 activation. In this study, Nec-1 reduced PARP activity but had no effect on the expression of PARP-1 in cells treated with glutamate. Nec-1 also did not protect against cell death mediated by the PARP activator N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), although PJ34 did protect against MNNG-mediated cell death. These findings suggest that Nec-1 is not a direct PARP inhibitor and that its signaling target is located upstream of PARP.
Citation Information
Xu, Xingshun; Chua, Chu C.; Zhang, Min; Geng, Deqin; Liu, Chun F.; Hamdy, Ronald C.; and Chua, Balvin H.L.. 2010. The Role of PARP Activation in Glutamate-Induced Necroptosis in HT-22 Cells. Brain Research. Vol.1343 206-212. https://doi.org/10.1016/j.brainres.2010.04.080 PMID: 20451505 ISSN: 0006-8993