Kondo M, Sumino R, Okado H
Department of Neurobiology, Tokyo Metropolitan Institute for Neuroscience, Fuchu, Tokyo 183, Japan.
J Neurosci. 1997 Mar 1;17(5):1570-81. doi: 10.1523/JNEUROSCI.17-05-01570.1997.
The functional properties of AMPA-type glutamate receptors are determined by their subunit composition. We detected the expression of the AMPA receptor subunits (GluR1-GluR4) in neurons in the somatosensory cortex of adult rats by combining nonradioactive in situ hybridization using digoxigenin-labeled RNA probes of GluR1 and GluR2 with immunocytochemistry using specific antibodies against GluR1, GluR2/3, and GluR4. On the basis of differential expression of the GluR1 and GluR2 subunits, we classified the cortical neurons into four categories. To correlate the differential expression of AMPA receptor subunits in each neuron with that of two calcium-binding proteins, parvalbumin and calbindin-D28k, we used a triple-labeling method. The majority of cortical neurons ( approximately 2/3) showed expression of GluR2 and undetectable expression of GluR1. GluR1-/GluR2-expressing neurons and GluR1-expressing/GluR2-undetectable neurons comprised approximately 1/10 each. Regarding the morphology, most GluR1-undetectable/GluR2-expressing neurons were pyramidal cells in layers II/III, V, and VI, whereas most GluR1-expressing/GluR2-undetectable neurons were nonpyramidal cells in layers II-VI. The GluR1-/GluR2-expressing neurons were either pyramidal or nonpyramidal. The majority of GluR1-/GluR2-expressing nonpyramidal cells was intensely stained with monoclonal antibody against calbindin-D28k, and one-half of the GluR1-undetectable/GluR2-expressing pyramidal neurons in layer II/III were lightly stained with this antibody. Most of GluR1-expressing/GluR2-undetectable neurons possessed parvalbumin immunoreactivity. These results indicate that neurons in the rat somatosensory cortex express differential combinations of GluR subunits, which correlate with the specific expression of the calcium-binding proteins.
AMPA 型谷氨酸受体的功能特性由其亚基组成决定。我们通过将使用地高辛标记的 GluR1 和 GluR2 RNA 探针的非放射性原位杂交与使用针对 GluR1、GluR2/3 和 GluR4 的特异性抗体的免疫细胞化学相结合,检测成年大鼠体感皮层神经元中 AMPA 受体亚基(GluR1 - GluR4)的表达。基于 GluR1 和 GluR2 亚基的差异表达,我们将皮层神经元分为四类。为了将每个神经元中 AMPA 受体亚基的差异表达与两种钙结合蛋白——小白蛋白和钙结合蛋白 - D28k 的差异表达相关联,我们使用了三重标记法。大多数皮层神经元(约 2/3)显示 GluR2 表达而 GluR1 表达不可检测。表达 GluR1 - /GluR2 的神经元和表达 GluR1/不表达 GluR2 的神经元各占约 1/10。在形态学方面,大多数不表达 GluR1/表达 GluR2 的神经元是位于 II/III、V 和 VI 层的锥体细胞,而大多数表达 GluR1/不表达 GluR2 的神经元是位于 II - VI 层的非锥体细胞。表达 GluR1 - /GluR2 的神经元要么是锥体细胞要么是非锥体细胞。大多数表达 GluR1 - /GluR2 的非锥体细胞被抗钙结合蛋白 - D28k 单克隆抗体强烈染色,并且 II/III 层中不表达 GluR1/表达 GluR2 的锥体细胞中有一半被该抗体轻度染色。大多数表达 GluR1/不表达 GluR2 的神经元具有小白蛋白免疫反应性。这些结果表明,大鼠体感皮层中的神经元表达 GluR 亚基的不同组合,这与钙结合蛋白的特异性表达相关。