Kozlovsky N, Belmaker R H, Agam G
Stanley Foundation International Research Center, Ben-Gurion University of the Negev, Beersheva, Israel.
Schizophr Res. 2001 Oct 1;52(1-2):101-5. doi: 10.1016/s0920-9964(00)00174-2.
Glycogen synthase kinase-3 (GSK-3) (EC 2.7.1.37) is a protein kinase highly abundant in brain and involved in signal transduction cascades of multiple cellular processes, particularly neurodevelopment. Two forms of the enzyme, GSK-3alpha and -3beta have been previously identified. We have previously reported reduced GSK-3beta protein levels in postmortem frontal cortex of schizophrenic patients. In an attempt to explore whether reduction of GSK-3beta levels is brain region specific we examined it in occipital cortex. In order to find out if the reduction in frontal cortex is reflected in altered activity we measured GSK-3 enzymatic activity in this brain region. Western-blot analysis of GSK-3beta was carried out in postmortem occipital cortex of 15 schizophrenic, 15 bipolar, and 15 unipolar patients, and 15 normal controls. GSK-3 activity was measured by quantitating the phosphorylation of the specific substrate phospho-CREB in the frontal cortex specimens. GSK-3beta levels in occipital cortex did not differ between the four diagnostic groups. GSK-3 activity in the frontal cortex of schizophrenic patients was 45% lower than that of normal controls (0.196+/-0.082 and 0.357+/-0.084 pmol/mg proteinxmin, respectively; Kruskal-Wallis analysis: chi-square=8.27, df=3, p=0.04). The other two diagnostic groups showed no difference from the control group. Our results are consistent with the notion that schizophrenia involves neurodevelopmental pathology.
糖原合酶激酶-3(GSK-3)(EC 2.7.1.37)是一种在大脑中高度丰富的蛋白激酶,参与多种细胞过程的信号转导级联反应,尤其是神经发育。此前已鉴定出该酶的两种形式,即GSK-3α和-3β。我们之前报道过,精神分裂症患者死后额叶皮质中GSK-3β蛋白水平降低。为了探究GSK-3β水平的降低是否具有脑区特异性,我们在枕叶皮质中进行了检测。为了弄清楚额叶皮质中的降低是否反映在活性改变上,我们测量了该脑区的GSK-3酶活性。对15例精神分裂症患者、15例双相情感障碍患者、15例单相情感障碍患者以及15例正常对照者的死后枕叶皮质进行了GSK-3β的蛋白质印迹分析。通过定量额叶皮质标本中特异性底物磷酸化CREB的磷酸化水平来测量GSK-3活性。在四个诊断组中,枕叶皮质中的GSK-3β水平没有差异。精神分裂症患者额叶皮质中的GSK-3活性比正常对照者低45%(分别为0.196±0.082和0.357±0.084 pmol/mg蛋白×分钟;Kruskal-Wallis分析:卡方=8.27,自由度=3,p=0.04)。其他两个诊断组与对照组没有差异。我们的结果与精神分裂症涉及神经发育病理学这一观点一致。