A murine dopamine neuron-specific cDNA library and microarray: increased COX1 expression during methamphetamine neurotoxicity

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 represen...

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Veröffentlicht in:Neurobiology of disease 2001-10, Vol.8 (5), p.822
Hauptverfasser: Barrett, T, Xie, T, Piao, Y, Dillon-Carter, O, Kargul, G J, Lim, M K, Chrest, F J, Wersto, R, Rowley, D L, Juhaszova, M, Zhou, L, Vawter, M P, Becker, K G, Cheadle, C, Wood, 3rd, W H, McCann, U D, Freed, W J, Ko, M S, Ricaurte, G A, Donovan, D M
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Sprache:eng
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Zusammenfassung: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 substantia 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.
ISSN:0969-9961
DOI:10.1006/nbdi.2001.0423