Singec Ilyas, Knoth Rolf, Ditter Margarethe, Volk Benedikt, Frotscher Michael
Institute of Anatomy and Cell Biology, University of Freiburg, D-79104 Freiburg, Germany.
J Comp Neurol. 2004 Nov 1;479(1):30-42. doi: 10.1002/cne.20302.
As a substrate of protein kinase C (PKC), neurogranin (NG) is involved in the regulation of calcium signaling and activity-dependent plasticity. Recently, we have shown that, in the rodent cerebellum, NG is exclusively expressed by gamma-aminobutyric acidergic Golgi cells, whereas, in the monkey cerebellum, brush cells were the only neuronal population expressing NG (Singec et al. [2003] J. Comp. Neurol. 459:278-289). In the present study, we analyzed the neocortical and hippocampal expression patterns of NG in adult mouse (C57Bl/6), rat (Wistar), and monkey (Cercopithecus aetiops). By using immunocytochemistry and nonradioactive in situ hybridization, we demonstrate strong NG expression by principal cells in different neocortical layers and in the hippocampus by granule cells of the dentate gyrus and pyramidal neurons of CA1-CA3. In contrast, double-labeling experiments in rodents revealed that neocortical and hippocampal interneurons expressing glutamate decarboxylase 67 (GAD67) were consistently devoid of NG. In addition, by using antibodies against parvalbumin, calbindin, and calretinin, we could demonstrate the absence of NG in interneurons of monkey frontal cortex and hippocampus. Together these findings corroborate the idea of different calcium signaling pathways in excitatory and inhibitory cells that may contribute to different modes of synaptic plasticity in these neurons.
作为蛋白激酶C(PKC)的底物,神经颗粒蛋白(NG)参与钙信号调节和活性依赖的可塑性。最近,我们发现,在啮齿动物小脑中,NG仅由γ-氨基丁酸能高尔基细胞表达,而在猴小脑中,刷细胞是唯一表达NG的神经元群体(Singec等人,[2003]《比较神经学杂志》459:278 - 289)。在本研究中,我们分析了成年小鼠(C57Bl/6)、大鼠(Wistar)和猴(猕猴)新皮质和海马中NG的表达模式。通过免疫细胞化学和非放射性原位杂交,我们证明了不同新皮质层的主要细胞以及海马齿状回颗粒细胞和CA1 - CA3锥体细胞中NG的强表达。相比之下,啮齿动物的双重标记实验显示,表达谷氨酸脱羧酶67(GAD67)的新皮质和海马中间神经元始终不表达NG。此外,通过使用抗小白蛋白、钙结合蛋白和钙视网膜蛋白的抗体,我们证明了猴额叶皮质和海马中间神经元中不存在NG。这些发现共同证实了兴奋性和抑制性细胞中不同钙信号通路的观点,这可能有助于这些神经元中不同的突触可塑性模式。