Suppression of p53-activated gene, PAG608, attenuates methamphetamine-induced neurotoxicity

被引:17
作者
Asanuma, Masato [1 ]
Miyazaki, Ikuko [1 ]
Higashi, Youichirou [1 ]
Diaz-Corrales, Francisco J. [1 ]
Shimizu, Masako [1 ]
Miyoshi, Ko [1 ]
Ogawa, Norio [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Brain Sci, Okayama 7008558, Japan
关键词
methamphetamine; PAG608; p53; monoamine; dopamine; neurotoxicity;
D O I
10.1016/j.neulet.2006.12.036
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The p53-activated gene 608 (PAG608) is a proapoptotic gene activated and regulated by p53 expression in oxidative stress-induced apoptosis of neuronal cells. In this study, we determined the role of PAG608 in methamphetamine-induced neurotoxicity. Treatment of mouse dopaminergic CATH.a cells with 2 mM methamphetamine increased PAG608 expression at 3 h followed by increase in phosphorylated p53 expression. Transient transfection of PAG608 antisense cDNA or RNA interference using PAG608 small interfering RNA significantly attenuated the dose-dependent decrease in cell viability of CATH.a cells by methamphetamine (1-4 mM) exposure. In monoaminergic neuronal B65 cells, which contain serotonin rather than dopamine, methamphetamine-induced cell death was also significantly but partially protected by transient transfection of PAG608 antisense cDNA. Furthermore, cell death of PC 12 cells produced by methamphetamine (1-5 mM) was almost completely prevented by stable expression of PAG608 antisense cDNA, compared with significant reduction of cell viability in control PC12 cells. Our results showed that suppression of PAG608 using transient and stable transfection with PAG608 anti sense cDNA or small interfering RNA attenuates methamphetamine-induced death of various monoaminergic neuronal cells, suggesting that methamphetamine neurotoxicity in monoaminergic cells is related, at least in part, to induction of PAG608 expression. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:263 / 267
页数:5
相关论文
共 10 条
[1]
Direct interactions of methamphetamine with the nucleus [J].
Asanuma, M ;
Hayashi, T ;
Ordonèz, SV ;
Ogawa, N ;
Cadet, JL .
MOLECULAR BRAIN RESEARCH, 2000, 80 (02) :237-243
[2]
Methamphetamine-induced increase in striatal p53 DNA-binding activity is attenuated in Cu,Zn-superoxide dismutase transgenic mice [J].
Asanuma, M ;
Miyazaki, I ;
Higashi, Y ;
Cadet, JL ;
Ogawa, N .
NEUROSCIENCE LETTERS, 2002, 325 (03) :191-194
[3]
Expression of cell death-associated phospho-c-Jun and p53-activated gene 608 in hippocampal CA1 neurons following global ischemia [J].
Gillardon, F ;
Spranger, M ;
Tiesler, C ;
Hossmann, KA .
MOLECULAR BRAIN RESEARCH, 1999, 73 (1-2) :138-143
[4]
Expression of redox factor-1, p53-activated gene 608 and caspase-3 messenger RNAs following repeated unilateral common carotid artery occlusion in gerbils -: Relationship to delayed cell injury and secondary failure of energy state [J].
Hermann, DM ;
Kuroiwa, T ;
Hata, R ;
Gillardon, F ;
Ito, U ;
Mies, G .
NEUROSCIENCE, 2001, 102 (04) :779-787
[5]
Inhibition of tyrosinase reduces cell viability in catecholaminergic neuronal cells [J].
Higashi, Y ;
Asanuma, M ;
Miyazaki, I ;
Ogawa, N .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (04) :1771-1774
[6]
The p53-activated gene, PAG608, requires a zinc finger domain for nuclear localization and oxidative stress-induced [J].
Higashi, Y ;
Asanuma, M ;
Miyazaki, I ;
Haque, ME ;
Fujita, N ;
Tanaka, K ;
Ogawa, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (44) :42224-42232
[7]
Hirata H, 1997, J NEUROCHEM, V69, P780
[8]
A novel p53-inducible gene, PAG608, encodes a nuclear zinc finger protein whose overexpression promotes apoptosis [J].
Israeli, D ;
Tessler, E ;
Haupt, Y ;
Elkeles, A ;
Wilder, S ;
Amson, R ;
Telerman, A ;
Oren, M .
EMBO JOURNAL, 1997, 16 (14) :4384-4392
[9]
Activation of p53 and its target genes p21WAF1/Cip1 PAG608/Wig-1 in ischemic preconditioning [J].
Tomasevic, G ;
Shamloo, M ;
Israeli, D ;
Wieloch, T .
MOLECULAR BRAIN RESEARCH, 1999, 70 (02) :304-313
[10]
Wig-1, a new p53-induced gene encoding a zinc finger protein [J].
VarmehZiaie, S ;
Okan, I ;
Wang, YS ;
Magnusson, KP ;
Warthoe, P ;
Strauss, M ;
Wiman, KG .
ONCOGENE, 1997, 15 (22) :2699-2704