Gene expression profiling in the post-mortem human brain - no cause for dismay

被引:121
作者
Bahn, S [1 ]
Augood, S
Standaert, DG
Starkey, M
Emson, PC
机构
[1] Babraham Inst, Dept Neurobiol, Cambridge CB2 4AT, England
[2] K Human Genome Mapping Project, Resource Ctr, Cambridge CB10 1SB, England
[3] Harvard Univ, Sch Med, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Neurol Serv, Boston, MA 02114 USA
[5] Addenbrookes Hosp, Dept Psychiat, Cambridge CB2 2QQ, England
基金
英国生物技术与生命科学研究理事会;
关键词
post-mortem; neuropsychiatric disorders; molecular biology; expression profiling; laser-capture microdissection;
D O I
10.1016/S0891-0618(01)00099-0
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
Global expression profiling techniques such as microarray technology promise to revolutionize biology. Soon it will be possible to investigate alterations at the transcript level of the entire human genome. There is great hope that these techniques will at last shed light on the pathological processes involved in complex neuropsychiatric disorders such as schizophrenia. These scientific advances in turn have re-kindled a great interest and demand for post-mortem brain tissue. Good quality post-mortem tissue undoubtedly is the fundamental prerequisite to investigate complex brain disorders with Molecular profiling techniques. In this review we show that post-mortem brain tissue can yield good quality mRNA and intact protein antigens which allow the successful application of traditional molecular biology methods as well as novel profiling techniques. We also consider the use of laser-capture microdissection on post-mortem tissue. This recently developed technique allows the experimenter to explore the molecular basis of cellular function at the single cell level. The combination of laser-capture microdissection with high throughput profiling techniques offers opportunities to obtain precise genetic fingerprints of individual neurons allowing comparisons of normal and pathological states. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 94
页数:16
相关论文
共 106 条
  • [1] Frontal lobe dysfunction in progressive supranuclear palsy: Evidence for oxidative stress and mitochondrial impairment
    Albers, DS
    Augood, SJ
    Park, LCH
    Browne, SE
    Martin, DM
    Adamson, J
    Hutton, M
    Standaert, DG
    Vonsattel, JPG
    Gibson, GE
    Beal, MF
    [J]. JOURNAL OF NEUROCHEMISTRY, 2000, 74 (02) : 878 - 881
  • [2] Evidence for oxidative stress in the subthalamic nucleus in progressive supranuclear palsy
    Albers, DS
    Augood, SJ
    Martin, DM
    Standaert, DG
    Vonsattel, JPG
    Beal, MF
    [J]. JOURNAL OF NEUROCHEMISTRY, 1999, 73 (02) : 881 - 884
  • [3] Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling
    Alizadeh, AA
    Eisen, MB
    Davis, RE
    Ma, C
    Lossos, IS
    Rosenwald, A
    Boldrick, JG
    Sabet, H
    Tran, T
    Yu, X
    Powell, JI
    Yang, LM
    Marti, GE
    Moore, T
    Hudson, J
    Lu, LS
    Lewis, DB
    Tibshirani, R
    Sherlock, G
    Chan, WC
    Greiner, TC
    Weisenburger, DD
    Armitage, JO
    Warnke, R
    Levy, R
    Wilson, W
    Grever, MR
    Byrd, JC
    Botstein, D
    Brown, PO
    Staudt, LM
    [J]. NATURE, 2000, 403 (6769) : 503 - 511
  • [4] IDENTIFIED CHOLINERGIC NEURONS IN THE ADULT-RAT BRAIN ARE ENRICHED IN GAP-43 MESSENGER-RNA - A DOUBLE IN-SITU HYBRIDIZATION STUDY
    AUGOOD, S
    ARBUTHNOTT, G
    EMSON, PC
    [J]. JOURNAL OF CHEMICAL NEUROANATOMY, 1995, 9 (01) : 17 - 26
  • [5] Reduction in enkephalin and substance P messenger RNA in the striatum of early grade Huntington's disease: A detailed cellular in situ hybridization study
    Augood, SJ
    Faull, RLM
    Love, DR
    Emson, PC
    [J]. NEUROSCIENCE, 1996, 72 (04) : 1023 - 1036
  • [6] Dopamine D-1 and D-2 receptor gene expression in the striatum in Huntington's disease
    Augood, SJ
    Faull, RLM
    Emson, PC
    [J]. ANNALS OF NEUROLOGY, 1997, 42 (02) : 215 - 221
  • [7] Augood SJ, 2000, J COMP NEUROL, V421, P247
  • [8] Expression of the early-onset torsion dystonia gene (DYT1) in human brain
    Augood, SJ
    Penney, JB
    Friberg, IK
    Breakefield, XO
    Young, AB
    Ozelius, LJ
    Standaert, DG
    [J]. ANNALS OF NEUROLOGY, 1998, 43 (05) : 669 - 673
  • [9] CELLULAR-LOCALIZATION OF ENKEPHALIN GENE-EXPRESSION IN MPTP-TREATED CYNOMOLGUS MONKEYS
    AUGOOD, SJ
    EMSON, PC
    MITCHELL, IJ
    BOYCE, S
    CLARKE, CE
    CROSSMAN, AR
    [J]. MOLECULAR BRAIN RESEARCH, 1989, 6 (01): : 85 - 92
  • [10] Banks RE, 1999, ELECTROPHORESIS, V20, P689, DOI 10.1002/(SICI)1522-2683(19990101)20:4/5<689::AID-ELPS689>3.0.CO