Department of Anatomy and Centre for Molecular Biology and Neuroscience, University of Oslo, N-0317 Oslo, Norway.
Cereb Cortex. 2012 May;22(5):1203-14. doi: 10.1093/cercor/bhr203. Epub 2011 Aug 1.
ATP is known to be coreleased with glutamate at certain central synapses. However, the nature of its release is controversial. Here, we demonstrate that ATP release from cultured rat hippocampal neurons is sensitive to RNAi-mediated knockdown of the recently identified vesicular nucleotide transporter (VNUT or SLC17A9). In the intact brain, light microscopy showed particularly strong VNUT immunoreactivity in the cerebellar cortex, the olfactory bulb, and the hippocampus. Using immunoelectron microscopy, we found VNUT immunoreactivity colocalized with synaptic vesicles in excitatory and inhibitory terminals in the hippocampal formation. Moreover, VNUT immunolabeling, unlike that of the vesicular glutamate transporter VGLUT1, was enriched in preterminal axons and present in postsynaptic dendritic spines. Immunoisolation of synaptic vesicles indicated presence of VNUT in a subset of VGLUT1-containing vesicles. Thus, we conclude that VNUT mediates transport of ATP into synaptic vesicles of hippocampal neurons, thereby conferring a purinergic phenotype to these cells.
三磷酸腺苷(ATP)已知在某些中枢突触中与谷氨酸共同释放。然而,其释放的性质存在争议。在这里,我们证明了从培养的大鼠海马神经元中释放的 ATP 对最近鉴定的囊泡核苷酸转运体(VNUT 或 SLC17A9)的 RNAi 介导的敲低敏感。在完整的大脑中,显微镜显示小脑皮层、嗅球和海马体中 VNUT 免疫反应性特别强。使用免疫电子显微镜,我们发现 VNUT 免疫反应性与海马结构中兴奋性和抑制性末端的突触小泡共定位。此外,VNUT 免疫标记与囊泡谷氨酸转运体 VGLUT1 不同,在末梢轴突中富集,并存在于突触后树突棘中。突触小泡的免疫分离表明 VNUT 存在于包含 VGLUT1 的囊泡的亚群中。因此,我们得出结论,VNUT 将 ATP 转运到海马神经元的突触小泡中,从而赋予这些细胞嘌呤能表型。