Nakanishi S, Maeda N, Mikoshiba K
Division of Regulation of Macromolecular Function, Osaka University, Suita, Japan.
J Neurosci. 1991 Jul;11(7):2075-86. doi: 10.1523/JNEUROSCI.11-07-02075.1991.
The immunohistochemical localization of P400/inositol 1,4,5-trisphosphate (InsP3) receptor protein was studied in developing and adult mouse brain by using monoclonal antibodies. The developmental expression pattern of P400/InsP3 receptor protein differed among different classes of neurons. It was first detected in the somata of immature Purkinje cells at embryonic day 17, in the ventrolateral region of the posterior vermis in the cerebellum. Axonal immunoreactivity within the cerebellar nuclei was first present at postnatal day 3. Neurons in the retrosplenial cortex, the anterior olfactory nucleus, and the CA1 region of the hippocampus expressed immunoreactivity earlier than other regions of the brain. In the adult brain, not only the Purkinje cell but also many other types of cells in many areas of the brain expressed P400/InsP3 receptor, though to a lesser extent. These included the neurons in the striatum, globus pallidus, nucleus accumbens septi, anterior olfactory nucleus, olfactory tubercle, precommissural hippocampus, hippocampus, substantia nigra, cerebral cortex, pons, and certain hypothalamic nuclei. Forebrain cortical regions that receive afferents from the olfactory bulb, such as the anterior olfactory nucleus, olfactory tubercle, prepiriform cortex, entorhinal cortex, and amygdala, exhibited distinct immunoreactivity, while olfactory bulb was almost devoid of staining. Immunoreactivity in the axonal pathways was also found in the limbic-hypothalamic pathways, strionigral projection, and part of the corpus callosum. Results of Western blot analysis and 3H-InsP3 binding assay were consistent with the qualitative regional differences of immunoreactivity demonstrated by immunohistochemical study. The location of InsP3 receptor in the brain correlates well with the InsP3 binding sites demonstrated by an autoradiographic study.
利用单克隆抗体研究了P400/肌醇1,4,5 -三磷酸(InsP3)受体蛋白在发育中和成年小鼠脑中的免疫组织化学定位。P400/InsP3受体蛋白的发育表达模式在不同类型的神经元中有所不同。它首先在胚胎第17天在小脑蚓部后外侧区域未成熟浦肯野细胞的胞体中被检测到。小脑核内的轴突免疫反应性最早在出生后第3天出现。扣带回后部皮质、前嗅核和海马CA1区的神经元比脑的其他区域更早表达免疫反应性。在成体脑中,不仅浦肯野细胞,而且脑的许多区域中的许多其他类型的细胞也表达P400/InsP3受体,尽管表达程度较低。这些细胞包括纹状体、苍白球、伏隔核、前嗅核、嗅结节、前连合前海马、海马、黑质、大脑皮质、脑桥和某些下丘脑核中的神经元。接受来自嗅球传入纤维的前脑皮质区域,如前嗅核、嗅结节、梨状前皮质、内嗅皮质和杏仁核,表现出明显的免疫反应性,而嗅球几乎没有染色。在边缘 - 下丘脑通路、纹状体黑质投射和胼胝体的一部分的轴突通路中也发现了免疫反应性。蛋白质印迹分析和3H - InsP3结合测定的结果与免疫组织化学研究所显示的免疫反应性的定性区域差异一致。脑中InsP3受体的定位与放射自显影研究显示的InsP3结合位点密切相关。