Pieribone Vincent A, Porton Barbara, Rendon Beatrice, Feng Jian, Greengard Paul, Kao Hung-Teh
The John B Pierce Laboratory, Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
J Comp Neurol. 2002 Dec 9;454(2):105-14. doi: 10.1002/cne.10417.
We have examined the distribution of synapsin III in the adult mouse brain. Expression of synapsin III was observed in puncta throughout the brain, but demonstrated greater regional variation than that of synapsins I or II. This punctate staining is typical for synaptic vesicle proteins located at nerve terminals. These findings are also consistent with the well-established role for synapsins in regulating neurotransmitter release. However, unexpectedly, synapsin III was also highly expressed in the cell body and processes of immature neurons in neurogenic regions of the adult brain, such as the hippocampal dentate gyrus, rostral migratory stream, and olfactory bulb. Many synapsin III-positive neurons also reacted with an antibody directed toward polysialylated-neuronal cell adhesion molecule, a marker of immature, migrating neurons. These results suggest that synapsin III may also play a role in adult neurogenesis.
我们研究了突触结合蛋白III在成年小鼠大脑中的分布情况。在整个大脑的小点状区域均观察到了突触结合蛋白III的表达,但其区域差异比突触结合蛋白I或II更大。这种点状染色是位于神经末梢的突触小泡蛋白的典型特征。这些发现也与突触结合蛋白在调节神经递质释放方面已确立的作用相一致。然而,出乎意料的是,突触结合蛋白III在成年大脑神经发生区域的未成熟神经元的细胞体和突起中也高度表达,如海马齿状回、吻侧迁移流和嗅球。许多突触结合蛋白III阳性神经元也与针对多唾液酸化神经元细胞粘附分子的抗体发生反应,多唾液酸化神经元细胞粘附分子是未成熟迁移神经元的标志物。这些结果表明,突触结合蛋白III可能在成体神经发生中也发挥作用。