Todd A J, Watt C, Spike R C, Sieghart W
Laboratory of Human Anatomy, University of Glasgow, United Kingdom.
J Neurosci. 1996 Feb 1;16(3):974-82. doi: 10.1523/JNEUROSCI.16-03-00974.1996.
To determine whether GABA and glycine can act as cotransmitters at synapses in the rat spinal cord, we have compared the ultrastructural distribution of GABAA-receptor beta 3 subunit with that of the glycine receptor-associated protein gephyrin and combined this with postembedding detection of GABA and glycine. We also used a dual-immunofluorescence method to confirm that gephyrin was associated with the glycine-receptor alpha 1 subunit throughout the cord. GABAA beta 3-subunit immunoreactivity was restricted primarily to synapses, and at a majority of these synapses the presynaptic axon was GABA-immunoreactive. Many synapses showed both GABAA beta 3 and gephyrin immunoreactivity, and at most of these synapses GABA and glycine were enriched in the presynaptic axon. These results strongly support the idea that cotransmission by GABA and glycine occurs in the spinal cord.
为了确定γ-氨基丁酸(GABA)和甘氨酸是否能在大鼠脊髓的突触处作为共同递质发挥作用,我们比较了GABAA受体β3亚基与甘氨酸受体相关蛋白桥连蛋白的超微结构分布,并将此与GABA和甘氨酸的包埋后检测相结合。我们还使用了双重免疫荧光法来证实桥连蛋白在整个脊髓中都与甘氨酸受体α1亚基相关联。GABAAβ3亚基免疫反应性主要局限于突触,并且在大多数这些突触中,突触前轴突呈GABA免疫反应性。许多突触同时显示出GABAAβ3和桥连蛋白免疫反应性,并且在大多数这些突触中,GABA和甘氨酸在突触前轴突中富集。这些结果有力地支持了GABA和甘氨酸在脊髓中共同传递的观点。