Kao Hung-Teh, Li Ping, Chao Helen M, Janoschka Stephen, Pham Kara, Feng Jian, Mcewen Bruce S, Greengard Paul, Pieribone Vincent A, Porton Barbara
Nathan Kline Institute for Psychiatric Research and the Department of Psychiatry, New York University School of Medicine, Orangeburg, New York 10962, USA.
J Comp Neurol. 2008 Apr 20;507(6):1860-70. doi: 10.1002/cne.21643.
Synapsin III is a synaptic vesicle-associated protein that is expressed in cells of the subgranular layer of the hippocampal dentate gyrus, a brain region known to sustain substantial levels of neurogenesis into adulthood. Here we tested the hypothesis that synapsin III plays a role in adult neurogenesis with synapsin III knockout and wild-type mice. Immunocytochemistry of the adult hippocampal dentate gyrus revealed that synapsin III colocalizes with markers of neural progenitor cell development (nestin, PSA-NCAM, NeuN, and Tuj1) but did not colocalize with markers of mitosis (Ki67 and PCNA). Because neurogenesis consists of a number of stages, the proliferation, survival, and differentiation of neural progenitor cells were systematically quantitated in the hippocampal dentate gyrus of adult synapsin III knockout and wild-type mice. We found a 30% decrease in proliferation and a 55% increase in survival of neural progenitor cells in synapsin III knockout mice. We also observed a 6% increase in the number of neural progenitor cells that differentiated into neurons. No difference in the volume of the dentate gyrus was observed between synapsin III knockout and wild-type mice. Collectively, our results demonstrate a novel role for synapsin III in regulating the proliferation of neural progenitor cells in the adult hippocampal dentate gyrus. These findings suggest a distinct function for this synaptic vesicle protein, in addition to its role in neurotransmission.
突触结合蛋白III是一种与突触小泡相关的蛋白质,在海马齿状回颗粒下层的细胞中表达,海马齿状回是一个已知在成年期仍维持大量神经发生水平的脑区。在此,我们用突触结合蛋白III基因敲除小鼠和野生型小鼠检验了突触结合蛋白III在成体神经发生中起作用的假说。对成年海马齿状回进行免疫细胞化学分析发现,突触结合蛋白III与神经祖细胞发育标志物(巢蛋白、多唾液酸神经细胞黏附分子、神经元核抗原和βIII微管蛋白)共定位,但不与有丝分裂标志物(Ki67和增殖细胞核抗原)共定位。由于神经发生由多个阶段组成,我们系统地定量分析了成年突触结合蛋白III基因敲除小鼠和野生型小鼠海马齿状回中神经祖细胞的增殖、存活和分化情况。我们发现,突触结合蛋白III基因敲除小鼠的神经祖细胞增殖减少了30%,存活增加了55%。我们还观察到分化为神经元的神经祖细胞数量增加了6%。突触结合蛋白III基因敲除小鼠和野生型小鼠之间齿状回体积没有差异。总体而言,我们的结果证明了突触结合蛋白III在调节成年海马齿状回神经祖细胞增殖中具有新作用。这些发现表明,这种突触小泡蛋白除了在神经传递中发挥作用外,还具有独特的功能。