NF-kappa B contributes to 6-hydroxydopainine-induced apoptosis of nigral dopaminergic neurons through p53

作者:Liang Zhong Qin; Li Yun Lin; Zhao Xi Lin; Han Rong; Wang Xiaom Xia; Wang Yumei; Chase Thomas N; Bennett M Catherine; Qin Zheng Hong*
来源:Brain Research, 2007, 1145: 190-203.
DOI:10.1016/j.brainres.2007.01.130

摘要

To evaluate the contribution of NF-kappa B and the NF-kappa B target gene p53 to nigral dopaminergic neuron degeneration in rodent models of Parkinson's disease, time-course of dopaminergic neuron loss as well as changes in the expression of some NF-kappa B-regulated proapoptotic proteins were assayed after unilateral infusion of 6-hydroxydopamine into rat medial forebrain bundle. Substantial loss of tyrosine hydroxylase immunoreactivity in nigral was observed 24 h after 6-hydroxydopamine treatment. The degenerative processes began 12 h after 6-hydroxydopamine administration as evidenced by a positive silver staining. Apoptotic death of dopaminergic neurons was suggested by the appearance of TUNEL-positive nuclei in substantia nigra and internucleosomal DNA fragmentation as detected by agarose gel electrophoresis. NF-kappa B activation in dopaminergic neurons as revealed by immunohistochemistry and electrophoresis mobility shift assay, began at 12 h after 6-hydroxydopamine administration. Levels of c-Myc and p53 immunore activities increased after 6-hydroxydopamine treatment, mainly in dopaminergic neurons as indicated by co-localization with tyrosine hydroxylase immunoreactivity. Blockade of NF-kappa B nuclear translocation with recombinant cell-permeable peptide NF-kappa B SN50 inhibited NF-kappa B nuclear translocation and p53 induction. SN50 and the p53 antagonist pifithrin-alpha significantly reduced nigral dopaminergic neuron degeneration. These results suggest that NF-kappa B activation contributes, at least in part, to oxidative stress-induced degeneration of dopaminergic neurons through a NF-kappa B-dependent p53-signaling pathway.