Estrogen decreases zinc transporter 3 expression and synaptic vesicle zinc levels in mouse brain

被引:135
作者
Lee, JY
Kim, JH
Hong, SH
Lee, JY
Cherny, RA
Bush, AI
Palmiter, RD
Koh, JY
机构
[1] Univ Ulsan, Coll Med, Natl Creat Res Initiat Ctr Study Cent Nervous Sys, Seoul 138736, South Korea
[2] Univ Ulsan, Coll Med, Dept Neurol, Seoul 138736, South Korea
[3] Univ Ulsan, Coll Med, Dept Obstet & Gynecol, Seoul 138736, South Korea
[4] Univ Melbourne, Dept Pathol, Parkville, Vic 3052, Australia
[5] Univ Melbourne, Mental Hlth Res Inst Victoria, Parkville, Vic 3052, Australia
[6] Harvard Univ, Sch Med, Dept Psychiat, Charlestown, MA 02129 USA
[7] Massachusetts Gen Hosp, Lab Oxidat Biol, Genet & Aging Res Unit, Charlestown, MA 02129 USA
[8] Univ Washington, Dept Biochem, Howard Hughes Med Inst, Seattle, WA 98195 USA
关键词
D O I
10.1074/jbc.M309730200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies suggest that female sex hormones modulate synaptic zinc levels, which may influence amyloid plaque formation and Alzheimer's disease progression. We examined the effects of ovariectomy and estrogen supplement on the levels of synaptic zinc and zinc transporter protein Znt3 in the brain. Ovariectomy was performed on 5-month-old mice, and 2 weeks later, pellets containing vehicle, low (0.18 mg/pellet), or high dose (0.72 mg) 17beta-estradiol were implanted. After 4 weeks, animals were decapitated, and blood and brain were collected for analysis. Blood analysis indicated that estrogen implants altered plasma estrogen levels in a dose-dependent manner. Analysis of brain tissue showed that ovariectomy raised hippocampal synaptic vesicle zinc levels, whereas estrogen replacement lowered these zinc levels. Western blots revealed that Znt3 levels in the brain were modulated in parallel with synaptic zinc levels, whereas no change was detected in the levels of Znt3 mRNA, as determined by Northern blot and reverse transcriptase-PCR analysis. However, mRNA levels of the delta subunit of adaptor protein complex (AP)-3, which modulates the level of Znt3 levels, were altered by estrogen depletion or replacement. These data demonstrate that estrogen alters the levels of Znt3 and synaptic vesicle zinc in female mice, probably through changing AP-3 delta expression. Since synaptic zinc may play a key role in neuronal death in acute brain injury as well as in plaque formation in Alzheimer's disease, and since estrogen may be beneficial in both conditions, our results may provide new insights into the effects of estrogen on the brain.
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收藏
页码:8602 / 8607
页数:6
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