Transcription factors specifying dopamine phenotype are decreased in cocaine users

被引:25
作者
Bannon, MJ
Pruetz, B
Barfield, E
Schmidt, CJ
机构
[1] Wayne State Univ, Sch Med, Dept Psychiat & Behav Neurosci, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Dept Pharmacol, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Dept Mol & Med Genet, Detroit, MI 48201 USA
[4] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48201 USA
关键词
cocaine; dopamine; engrailed; human; Nurr1; Pitx3; postmortem; substantia nigra; transcription;
D O I
10.1097/00001756-200403010-00003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During development, survival of midbrain dopamine neurons and specification of their phenotype are dependent upon the intracellular expression of a number of transcription factors, including Engrailed 1, Pitx3, and Nurr1. The role of these transcription factors in the maintenance of the dopaminergic phenotype is less clear. In the present study, we show that each of these transcription factors is robustly expressed in adult dopamine neurons in human midbrain, and that cocaine abuse is associated with a significant decrease in the abundance of Nurr1 and Pitx3 in these cells. These data suggest that cocaine abuse leads to a partial loss of dopaminergic phenotype.
引用
收藏
页码:401 / 404
页数:4
相关论文
共 29 条
[1]   Age-related and regional differences in dopamine transporter mRNA expression in human midbrain [J].
Bannon, MJ ;
Whitty, CJ .
NEUROLOGY, 1997, 48 (04) :969-977
[2]   Decreased expression of the transcription factor NURR1 in dopamine neurons of cocaine abusers [J].
Bannon, MJ ;
Pruetz, B ;
Manning-Bog, AB ;
Whitty, CJ ;
Michelhaugh, SK ;
Sacchetti, P ;
Granneman, JG ;
Mash, DC ;
Schmidt, CJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (09) :6382-6385
[3]   Dopamine biosynthesis is selectively abolished in substantia nigra ventral tegmental area but not in hypothalamic neurons in mice with targeted disruption of the Nurr1 gene [J].
Castillo, SO ;
Baffi, JS ;
Palkovits, M ;
Goldstein, DS ;
Kopin, IJ ;
Witta, J ;
Magnuson, MA ;
Nikodem, VM .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1998, 11 (1-2) :36-46
[4]   A response element for the homeodomain transcription factor Ptx3 in the tyrosine hydroxylase gene promoter [J].
Cazorla, P ;
Smidt, MP ;
O'Malley, KL ;
Burbach, JPH .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (05) :1829-1837
[5]   Age-related decreases in Nurr1 immunoreactivity in the human substantia nigra [J].
Chu, YP ;
Kompoliti, K ;
Cochran, EJ ;
Mufson, EJ ;
Kordower, JH .
JOURNAL OF COMPARATIVE NEUROLOGY, 2002, 450 (03) :203-214
[6]   Nurr1-null heterozygous mice have reduced mesolimbic and mesocortical dopamine levels and increased stress-induced locomotor activity [J].
Eells, JB ;
Lipska, BK ;
Yeung, SK ;
Misler, JA ;
Nikodem, VM .
BEHAVIOURAL BRAIN RESEARCH, 2002, 136 (01) :267-275
[7]   Specification of catecholaminergic and serotonergic neurons [J].
Goridis, C ;
Rohrer, H .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (07) :531-541
[8]   Selective loss of dopaminergic neurons in the substantia nigra of Pitx3-deficient aphakia mice [J].
Hwang, DY ;
Ardayfio, P ;
Kang, UJ ;
Semina, EV ;
Kim, KS .
MOLECULAR BRAIN RESEARCH, 2003, 114 (02) :123-131
[9]   Specification of dopaminergic and serotonergic neurons in the vertebrate CNS [J].
Hynes, M ;
Rosenthal, A .
CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (01) :26-36
[10]   Identification of a potential Nurr1 response element that activates the tyrosine hydroxylase gene promoter in cultured cells [J].
Iwawaki, T ;
Kohno, K ;
Kobayashi, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 274 (03) :590-595