Petralia R S, Wang Y X, Niedzielski A S, Wenthold R J
Laboratory of Neurochemistry, NIDCD, NIH, Bethesda, MD 20892, USA.
Neuroscience. 1996 Apr;71(4):949-76. doi: 10.1016/0306-4522(95)00533-1.
Glutamate neurotransmission involves numerous ionotropic and metabotropic glutamate receptor types in postsynaptic, presynaptic and glial locations. Distribution of the metabotropic glutamate receptors mGluR2 and mGluR3 was studied with an affinity-purified, characterized polyclonal antibody made from a C-terminus peptide. This antibody, mGluR2/3, recognized both mGluR2 and mGluR3, but did not cross-react with any other type of metabotropic glutamate receptor except for a very slight recognition of mGluR5. Light microscope distribution of the antibody binding sites in the nervous system matched the combined distributions of messenger RNA for mGluR2 and mGluR3. For example, dense staining seen in the accessory olfactory bulb and cerebellar Golgi cells matched high levels of mGluR2 messenger RNA in these structures, while moderately dense staining in the reticular nucleus of the thalamus and light to moderate staining in glia throughout the brain matched significant levels of mGluR3 messenger RNA in these structures. In the rostral olfactory structures, the densest stained neurons belonged to presumptive "necklace olfactory glomeruli." In the hippocampus, staining was densest in the neuropil of the stratum lucidum/pyramidale, stratum lacunosum/moleculare, hilus and middle third of the molecular layer of the dentate gyrus. Ultrastructural studies of the cerebral cortex, hippocampus and caudate-putamen revealed significant staining in postsynaptic and presynaptic structures and glial wrappings of presumptive excitatory synapses; frequently, this staining was concentrated in discrete patches at or near active zones. In the hippocampus, presynaptic staining appeared to be concentrated in terminals of two populations of presumptive glutamatergic axons: mossy fibers originating from granule cells and perforant path fibers originating from the entorhinal cortex. These data suggest that populations of mGluR2 and/or mGluR3 receptors are localized differentially in synapses, i.e. those in and near the postsynaptic and presynaptic membranes and in glial wrappings of synapses, in several regions of the brain. In addition, we provide immunocytochemical evidence of mGluR2 or mGluR3 receptors in presynaptic terminals of glutamatergic synapses. Thus, mGluR2 and mGluR3 are found in various combinations of presynaptic, postsynaptic and glial localizations that may reflect differential modulation of excitatory amino acid transmission.
谷氨酸神经传递涉及突触后、突触前和神经胶质部位的多种离子型和代谢型谷氨酸受体类型。利用从C端肽制备的亲和纯化、特性明确的多克隆抗体,研究了代谢型谷氨酸受体mGluR2和mGluR3的分布。这种抗体mGluR2/3能识别mGluR2和mGluR3,但除了对mGluR5有非常轻微的识别外,不与任何其他类型的代谢型谷氨酸受体发生交叉反应。抗体结合位点在神经系统中的光学显微镜分布与mGluR2和mGluR3信使RNA的联合分布相匹配。例如,在副嗅球和小脑高尔基细胞中看到的密集染色与这些结构中高水平的mGluR2信使RNA相匹配,而丘脑网状核中的中度密集染色以及整个大脑神经胶质中的轻度至中度染色与这些结构中显著水平的mGluR3信使RNA相匹配。在吻侧嗅觉结构中,染色最密集的神经元属于假定的“项链状嗅觉小球”。在海马体中,染色最密集的部位是透明层/锥体层、腔隙层/分子层的神经毡、齿状回的门区和分子层的中三分之一。对大脑皮层、海马体和尾状核-壳核的超微结构研究显示,在假定的兴奋性突触的突触后和突触前结构以及神经胶质包裹物中有显著染色;这种染色通常集中在活跃区或其附近的离散斑块中。在海马体中,突触前染色似乎集中在两类假定的谷氨酸能轴突的终末:起源于颗粒细胞的苔藓纤维和起源于内嗅皮质的穿通通路纤维。这些数据表明,mGluR2和/或mGluR3受体群体在突触中存在差异定位,即在几个脑区的突触后膜和突触前膜内及附近以及突触的神经胶质包裹物中。此外,我们提供了谷氨酸能突触前终末中mGluR2或mGluR3受体的免疫细胞化学证据。因此,mGluR2和mGluR3存在于突触前、突触后和神经胶质定位的各种组合中,这可能反映了兴奋性氨基酸传递的差异调节。