Glycogen synthase kinase-3β immunoreactivity is reduced in the prefrontal cortex in schizophrenia

被引:103
作者
Beasley, C
Cotter, D
Khan, N
Pollard, C
Sheppard, P
Varndell, I
Lovestone, S
Anderton, B
Everall, I
机构
[1] Inst Psychiat, Dept Neuropathol, London SE5 8AF, England
[2] Inst Psychiat, Dept Med Psychol, London SE5 8AF, England
[3] Inst Psychiat, Dept Neurosci, London SE5 8AF, England
[4] Affiniti Res Prod Ltd, Exeter EX6 8HD, Devon, England
基金
英国医学研究理事会;
关键词
GSK-3; beta; beta-catenin; dishevelled; Wnt signalling; schizophrenia; frontal cortex;
D O I
10.1016/S0304-3940(01)01688-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cytoarchitectural abnormalities have been reported in the cortex in schizophrenia. These suggest a developmental origin for this disorder. The Wnt signalling pathway is involved in the regulation of brain development; disruption of this pathway may lead to abnormal cortical development. In this study levels of three components of the Wnt signalling pathway; glycogen synthase kinase-3 beta (GSK-3 beta), beta -catenin and dishevelled-2 (Dvl-2) were determined in the prefrontal cortex of ten schizophrenic and ten control individuals using immunoblotting. GSK-3 beta levels were significantly reduced in the schizophrenic group, while levels of beta -catenin and Dvl-2 did not differ between groups. This provides further evidence for an abnormality of the Wnt signalling pathway in schizophrenia. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:117 / 120
页数:4
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