A murine dopamine neuron-specific cDNA library and microarray: Increased COXI expression during methamphetamine neurotoxicity

被引:26
作者
Barrett, T
Xie, T
Piao, Y
Dillon-Carter, O
Kargul, GJ
Lim, MK
Chrest, FJ
Wersto, R
Rowley, DL
Juhaszova, M
Zhou, L
Vawter, MP
Becker, KG
Cheadle, C
Wood, WH
McCann, UD
Freed, WJ
Ko, MS
Ricaurte, GA
Donovan, DM
机构
[1] NIA, Intramural Res Program, Res Resources Branch, NIH, Baltimore, MD 21224 USA
[2] NIA, Genet Lab, NIH, Baltimore, MD 21224 USA
[3] NIDA, Cellular Neurobiol Branch, NIH, Baltimore, MD 21224 USA
[4] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD 21205 USA
关键词
dopamine; cDNA library; cDNA microarray; methamphetamine; development; gene expression profile;
D O I
10.1006/nbdi.2001.0423
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Due to brain tissue heterogeneity, the molecular genetic profile of any neurotransmitter-specific neuronal subtype is unknown. The purpose of this study was to purify a population of dopamine neurons, construct a cDNA library, and generate an initial gene expression profile and a microarray representative of dopamine neuron transcripts. Ventral mesencephalic dopamine neurons were purified by fluorescent-activated cell sorting from embryonic day 13.5 transgenic mice harboring a 4.5-kb rat tyrosine hydroxylase promoter-lacZ fusion. Nine-hundred sixty dopamine neuron cDNA clones were sequenced and arrayed for use in studies of gene expression changes during methamphetamine neurotoxicity. A neurotoxic dose of methamphetamine produced a greater than twofold up-regulation of the mitochondrial cytochrome c oxidase polypeptide I transcript from adult mouse substantial nigra at 12 h posttreatment. This is the first work to describe a gene expression profile for a neuronal subtype and to identify gene expression changes during methamphetamine neurotoxicity. (C) 2001 Academic Press.
引用
收藏
页码:822 / 833
页数:12
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