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PEP-1-p18 prevents neuronal cell death by inhibiting oxidative stress and Bax expression

Authors
Kim, Duk-SooSohn, Eun JeongKim, Dae WonKim, Young NamEom, Seon AeYoon, Ga HyeonCho, Sung-WooLee, Sang-HyunHwang, Hyun SookCho, Yoon ShinPark, JinseuEum, Won SikChoi, Soo Young
Issue Date
30-Sep-2012
Publisher
생화학분자생물학회
Keywords
Cell viability; Parkinson's disease; PEP-1-p18; Protein therapy; Protein transduction
Citation
BMB Reports, v.45, no.9, pp 532 - 537
Pages
6
Journal Title
BMB Reports
Volume
45
Number
9
Start Page
532
End Page
537
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/14830
DOI
10.5483/BMBRep.2012.45.9.083
ISSN
1976-6696
1976-670X
Abstract
P18, a member of the INK4 family of cyclin-dependent kinase inhibitors, is a tumor suppressor protein and plays a key cell survival role in a variety of human cancers. Under pathophysiological conditions, the INK4 group proteins participate in novel biological functions associated with neuronal diseases and oxidative stress. Parkinson's disease (PD) is characterized by loss of dopaminergic neurons, and oxidative stress is important in its pathogenesis. Therefore, we examined the effects of PEP-1-p18 on oxidative stress-induced SH-SY5Y cells and in a PD mouse model. The transduced PEP-1-p18 markedly inhibited 1-methyl-4-phenyl pyridinium-induced SH-SY5Y cell death by inhibiting Bax expression levels and DNA fragmentation. Additionally, PEP-1-p18 prevented dopaminergic neuronal cell death in the substantia nigra of a 1-methyl-4-phenyl-1,2,3,6,-tetrahydropyridine-induced PD mouse model. These results indicate that PEP-1-p18 may be a useful therapeutic agent against various diseases and is a potential tool for treating PD. [BMB Reports 2012; 45(9): 532-537]
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