Adult neurogenesis and schizophrenia: A window on abnormal early brain development?

被引:76
作者
Toro, C. T. [1 ]
Deakin, J. F. W. [1 ]
机构
[1] Univ Manchester, Neurosci & Psychiat Unit, Manchester M13 9PT, Lancs, England
关键词
schizophrenia; neurogenesis; post-mortem brains; doublecortin;
D O I
10.1016/j.schres.2006.09.030
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Adult neurogenesis is one of the most rapidly growing areas in neuroscience research and there is great interest in its potential role in the pathophysiology of psychiatric illness. In parallel with early development, adult neurogenesis occurs through the proliferation of precursor cells which migrate to specific regions and differentiate into neurons with characteristics indistinguishable from existing mature neurons. These findings have led to the re-definition of the concept of network plasticity in the adult brain, to include the formation of new neurons as well as new connections. This review examines the idea that adult neurogenesis may be disturbed in schizophrenia. We discuss evidence for abnormal mechanisms of neurogenesis and expression of developmental genes in schizophrenia, the influence of antipsychotic drugs on neurogenesis and the role of candidate schizophrenia susceptibility genes in adult neurogenesis. The recent discovery of molecular markers transiently expressed in newbom neurons within adult neurogenic brain regions could be used to probe whether neurogenesis is disturbed in schizophrenia. Adult neurogenesis could also be used as a unique tool for investigating genes involved in early brain development using post-mortem brains. This is particularly relevant for brain disorders with developmental origins such as schizophrenia. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 130 条
[1]   Adult neurogenesis: From precursors to network and physiology [J].
Abrous, DN ;
Koehl, M ;
Le Moal, M .
PHYSIOLOGICAL REVIEWS, 2005, 85 (02) :523-569
[2]   Cytoplasmic dynein and dynactin are required for the transport of microtubules into the axon [J].
Ahmad, FJ ;
Echeverri, CJ ;
Vallee, RB ;
Baas, PW .
JOURNAL OF CELL BIOLOGY, 1998, 140 (02) :391-401
[3]  
Alcántara S, 1998, J NEUROSCI, V18, P7779
[4]   The effects of antipsychotics on β-catenin, glycogen synthase kinase-3 and dishevelled in the ventral midbrain of rats [J].
Alimohamad, H ;
Sutton, L ;
Mouyal, J ;
Rajakumar, N ;
Rushlow, WJ .
JOURNAL OF NEUROCHEMISTRY, 2005, 95 (02) :513-525
[5]   Deficient hippocampal neuron expression of proteasome, ubiquitin, and mitochondrial genes in multiple schizophrenia cohorts [J].
Altar, CA ;
Jurata, LW ;
Charles, V ;
Lemire, A ;
Liu, P ;
Bukhman, Y ;
Young, TA ;
Bullard, J ;
Yokoe, H ;
Webster, MJ ;
Knable, MB ;
Brockman, JA .
BIOLOGICAL PSYCHIATRY, 2005, 58 (02) :85-96
[6]   AUTORADIOGRAPHIC AND HISTOLOGICAL EVIDENCE OF POSTNATAL HIPPOCAMPAL NEUROGENESIS IN RATS [J].
ALTMAN, J ;
DAS, GD .
JOURNAL OF COMPARATIVE NEUROLOGY, 1965, 124 (03) :319-&
[7]   Neurodevelopment, neuroplasticity, and new genes for schizophrenia [J].
Arnold, SE ;
Talbot, K ;
Hahn, CG .
DEVELOPMENT, DYNAMICS AND PATHOLOGY OF NEURONAL NETWORKS: FROM MOLECULES TO FUNCTIONAL CIRCUITS, 2005, 147 :319-345
[8]   Dysregulation of olfactory receptor neuron lineage in schizophrenia [J].
Arnold, SE ;
Han, LY ;
Moberg, PJ ;
Turetsky, BI ;
Gur, RE ;
Trojanowski, JQ ;
Hahn, CG .
ARCHIVES OF GENERAL PSYCHIATRY, 2001, 58 (09) :829-835
[9]   Expression of disrupted-in-schizophrenia-1, a schizophrenia-associated gene, is prominent in the mouse hippocampus throughout brain development [J].
Austin, CP ;
Ky, B ;
Ma, L ;
Morris, JA ;
Shughrue, PJ .
NEUROSCIENCE, 2004, 124 (01) :3-10
[10]   DISC1 (Disrupted in Schizophrenia-1) is expressed in limbic regions of the primate brain [J].
Austin, CP ;
Ma, L ;
Ky, B ;
Morris, JA ;
Shughrue, PJ .
NEUROREPORT, 2003, 14 (07) :951-954