Racca C, Gardiol A, Triller A
Laboratoire de Biologie Cellulaire de la Synapse, INSERM, CJF 94-10, Ecole Normale Supérieure, 75005 Paris, France.
J Neurosci. 1997 Mar 1;17(5):1691-700. doi: 10.1523/JNEUROSCI.17-05-01691.1997.
Some synaptic neurotransmitter receptors, such as those for glycine, have somato-dendritic distributions. Although the machinery for protein synthesis and several mRNAs are present in dendrites and close to synapses in central neurons, so far the mRNAs for neurotransmitter receptors have not been found unequivocally in dendrites. The glycine receptor (GlyR), a ligand-gated channel mediating a chloride-dependent inhibition, is composed of transmembrane alpha and beta subunits. GlyRs are only present at glycinergic postsynaptic differentiation, where they are stabilized by the associated protein gephyrin. With light nonradioactive in situ hybridization (ISH), we observe that GlyR alpha subunit mRNAs are present in both somata and dendrites of most neurons of the ventral horn of rat spinal cord, whereas the beta subunit and gephyrin mRNAs are predominantly in somata. Interestingly, within dendrites GlyR alpha subunit mRNAs form aggregates that are mostly localized peripherally to the dendritic axial core. Electron microscopic ISH shows that GlyR alpha subunit mRNAs are associated with postsynaptic differentiations. At these sites, the GlyR alpha subunit mRNAs are detected in close association with subsynaptic cisternae. This targeting of alpha subunit mRNAs to postsynaptic domains could provide a means of dynamically modulating synaptic efficacy by changing the composition and the density of receptors at glycinergic synapses.
一些突触神经递质受体,如甘氨酸受体,具有体树突分布。尽管在中枢神经元的树突中以及靠近突触处存在蛋白质合成机制和几种mRNA,但到目前为止,尚未在树突中明确发现神经递质受体的mRNA。甘氨酸受体(GlyR)是一种介导氯离子依赖性抑制的配体门控通道,由跨膜α和β亚基组成。GlyRs仅存在于甘氨酸能突触后分化部位,在那里它们通过相关蛋白gephyrin得以稳定。通过轻度非放射性原位杂交(ISH),我们观察到甘氨酸受体α亚基mRNA存在于大鼠脊髓腹角大多数神经元的胞体和树突中,而β亚基和gephyrin mRNA主要存在于胞体中。有趣的是,在树突内,甘氨酸受体α亚基mRNA形成聚集体,大多位于树突轴芯的周边。电子显微镜原位杂交显示甘氨酸受体α亚基mRNA与突触后分化相关。在这些部位,可检测到甘氨酸受体α亚基mRNA与突触下池紧密相连。α亚基mRNA靶向突触后结构域可能提供了一种通过改变甘氨酸能突触处受体的组成和密度来动态调节突触效能的方式。