Weickert C S, Hyde T M, Lipska B K, Herman M M, Weinberger D R, Kleinman J E
Clinical Brain Disorders Branch, NIMH, IRP, NIH, Bethesda, MD 20892-1385, USA.
Mol Psychiatry. 2003 Jun;8(6):592-610. doi: 10.1038/sj.mp.4001308.
Anatomical and molecular abnormalities of excitatory neurons in the dorsolateral prefrontal cortex (DLPFC) are found in schizophrenia. We hypothesized that brain-derived neurotrophic factor (BDNF), a protein capable of increasing pyramidal neuron spine density and augmenting synaptic efficacy of glutamate, may be abnormally expressed in the DLPFC of patients with schizophrenia. Using an RNase protection assay and Western blotting, we detected a significant reduction in BDNF mRNA (mean=23%) and protein (mean=40%) in the DLPFC of patients with schizophrenia compared to normal individuals. At the cellular level, BDNF mRNA was expressed at varying intensities in pyramidal neurons throughout layers II, III, V, and VI of DLPFC. In patients with schizophrenia; neuronal BDNF expression was decreased in layers III, V and VI. Our study demonstrates a reduction in BDNF production and availability in the DLPFC of schizophrenics, and suggests that intrinsic cortical neurons, afferent neurons, and target neurons may receive less trophic support in this disorder.
在精神分裂症患者中发现背外侧前额叶皮质(DLPFC)兴奋性神经元存在解剖学和分子学异常。我们推测,脑源性神经营养因子(BDNF),一种能够增加锥体神经元棘突密度并增强谷氨酸突触效能的蛋白质,在精神分裂症患者的DLPFC中可能异常表达。使用核糖核酸酶保护分析和蛋白质印迹法,我们检测到与正常个体相比,精神分裂症患者DLPFC中BDNF mRNA(平均降低23%)和蛋白质(平均降低40%)显著减少。在细胞水平上,BDNF mRNA在DLPFC的II、III、V和VI层的锥体神经元中以不同强度表达。在精神分裂症患者中,III、V和VI层的神经元BDNF表达降低。我们的研究表明,精神分裂症患者DLPFC中BDNF的产生和可用性降低,这表明在这种疾病中,皮质固有神经元、传入神经元和靶神经元可能接受较少的营养支持。