Beasley C, Cotter D, Khan N, Pollard C, Sheppard P, Varndell I, Lovestone S, Anderton B, Everall I
Department of Neuropathology, Institute of Psychiatry, DeCrespigny Park, SE5 8AF, London, UK.
Neurosci Lett. 2001 Apr 20;302(2-3):117-20. doi: 10.1016/s0304-3940(01)01688-3.
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-3beta(GSK-3beta), beta-catenin and dishevelled-2 (Dvl-2) were determined in the prefrontal cortex of ten schizophrenic and ten control individuals using immunoblotting. GSK-3beta 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.
在精神分裂症患者的大脑皮层中,已发现细胞结构异常。这些异常表明该疾病起源于发育过程。Wnt信号通路参与大脑发育的调控;该通路的破坏可能导致皮层发育异常。在本研究中,采用免疫印迹法测定了10名精神分裂症患者和10名对照者前额叶皮层中Wnt信号通路的三个成分,即糖原合酶激酶-3β(GSK-3β)、β-连环蛋白和散乱蛋白-2(Dvl-2)的水平。精神分裂症组GSK-3β水平显著降低,而β-连环蛋白和Dvl-2水平在两组间无差异。这为精神分裂症中Wnt信号通路异常提供了进一步的证据。