Patterns of gene expression are altered in the frontal and motor cortices of human alcoholics

被引:262
作者
Mayfield, RD
Lewohl, JM
Dodd, PR
Herlihy, A
Liu, JW
Harris, RA
机构
[1] Univ Texas, Waggoner Ctr Alcohol & Addict Res, Austin, TX 78712 USA
[2] Univ Queensland, Dept Biochem, St Lucia, Qld, Australia
关键词
alcoholism; brain; ethanol; gene expression; human; microarray;
D O I
10.1046/j.1471-4159.2002.00860.x
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
Alcoholism is a major health problem in Western countries, yet relatively little is known about the mechanisms by which chronic alcohol abuse causes the pathologic changes associated with the disease. It is likely that chronic alcoholism affects a number of signaling cascades and transcription factors, which in turn result in distinct gene expression patterns. These patterns are difficult to detect by traditional experiments measuring a few mRNAs at a time, but are well suited to microarray analyses. We used cDNA microarrays to analyze expression of approximately 10 000 genes in the frontal and motor cortices of three groups of chronic alcoholic and matched control cases. A functional hierarchy was devised for classification of brain genes and the resulting groups were compared based on differential expression. Comparison of gene expression patterns in these brain regions revealed a selective reprogramming of gene expression in distinct functional groups. The most pronounced differences were found in myelin-related genes and genes involved in protein trafficking. Significant changes in the expression of known alcohol-responsive genes, and genes involved in calcium, cAMP, and thyroid signaling pathways were also identified. These results suggest that multiple pathways may be important for neuropathology and altered neuronal function observed in alcoholism.
引用
收藏
页码:802 / 813
页数:12
相关论文
共 47 条
  • [1] Gene expression profiling in the post-mortem human brain - no cause for dismay
    Bahn, S
    Augood, S
    Standaert, DG
    Starkey, M
    Emson, PC
    [J]. JOURNAL OF CHEMICAL NEUROANATOMY, 2001, 22 (1-2) : 79 - 94
  • [2] DISRUPTION OF THE COMPACTED MYELIN SHEATH OF AXONS OF THE CENTRAL-NERVOUS-SYSTEM IN PROTEOLIPID PROTEIN-DEFICIENT MICE
    BOISON, D
    STOFFEL, W
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) : 11709 - 11713
  • [3] α-Synuclein and parkin:: coming together of pieces in puzzle of Parkinson's disease
    Burke, RE
    [J]. LANCET, 2001, 358 (9293) : 1567 - 1568
  • [4] Differential expression of NPY and its receptors in alcohol-preferring AA and alcohol-avoiding ANA rats
    Caberlotto, L
    Thorsell, A
    Rimondini, R
    Sommer, W
    Hyytiä, P
    Heilig, M
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2001, 25 (11) : 1564 - 1569
  • [5] Gene expression profiling in postmortem Rett syndrome brain: Differential gene expression and patient classification
    Colantuoni, C
    Jeon, OH
    Hyder, K
    Chenchik, A
    Khimani, AH
    Narayanan, V
    Hoffman, EP
    Kaufmann, WE
    Naidu, S
    Pevsner, J
    [J]. NEUROBIOLOGY OF DISEASE, 2001, 8 (05) : 847 - 865
  • [6] Expression profiling identifies strain-specific changes associated with ethanol withdrawal in mice
    Daniels, GM
    Buck, KJ
    [J]. GENES BRAIN AND BEHAVIOR, 2002, 1 (01) : 35 - 45
  • [7] De los Monteros AE, 1999, NEUROCHEM RES, V24, P235
  • [8] Cellular and molecular neuroscience of alcoholism
    Diamond, I
    Gordon, AS
    [J]. PHYSIOLOGICAL REVIEWS, 1997, 77 (01) : 1 - 20
  • [9] Cholesterol metabolism in the brain
    Dietschy, JM
    Turley, SD
    [J]. CURRENT OPINION IN LIPIDOLOGY, 2001, 12 (02) : 105 - 112
  • [10] Neuropeptide Y levels in ethanol-naive, alcohol-preferring, and nonpreferring rats and in Wistar rats after ethanol exposure
    Ehlers, CL
    Li, TK
    Lumeng, L
    Hwang, BH
    Somes, C
    Jimenez, P
    Mathé, AA
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1998, 22 (08) : 1778 - 1782