Toida K, Kosaka K, Heizmann C W, Kosaka T
Department of Anatomy and Neurobiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Neuroscience. 1996 May;72(2):449-66. doi: 10.1016/0306-4522(95)00521-8.
Neurons containing a calcium-binding protein parvalbumin in the external plexiform layer of the rat olfactory bulb were identified light microscopically with the pre-embedding immunocytochemistry and were subsequently analysed with the electron microscopic serial-sectioning and three-dimensional reconstructions. In the present study we chose several different types of parvalbumin-immunoreactive neurons identified light microscopically as Van Gehuchten cell type, superficial short-axon cell type and multipolar cell type. Parvalbumin-immunoreactive somata were similar to one another in their ultrastructural characteristics, showing nuclear indentations, moderately developed Golgi apparatus and abundant mitochondria; these structural features appeared to resemble those of the short axon cells around the glomeruli and in the granule cell layer reported in previous electron microscopic studies. All neurons analysed in the present study made symmetrical synapses on to dendrites and somata of presumed mitral/tufted cells and received asymmetrical synapses from them, and occasionally formed reciprocal synapses with them. On the parvalbumin-immunoreactive processes, the asymmetrical synapses nearly equalled the symmetrical ones in number and about 30-50% of them were identified as reciprocal pairs. In contrast, no presynaptic sites were observed on parvalbumin-immunoreactive somata, and thick portions (more than approximately 2 microns in diameter) of the proximal dendrites, where they were occasionally postsynaptic in some asymmetrical and symmetrical synapses from parvalbumin-immunonegative profiles. Characteristically, parvalbumin-immunoreactive process frequently make direct contacts with one another; processes regarded light microscopically as arising from a soma or a dendrite or parvalbumin-immunoreactive neurons were sometimes revealed to be separate but directly contacting processes with electron microscopic examinations. Although puncta adherentia were occasionally observed between these contact sites, so far neither gap junctions nor chemical synapses were observed. Until now, it has been believed that in the external plexiform layer only granule cells form reciprocal synapses with mitral/tufted cells. However, the present study clearly demonstrates that interneurons different from granule cells, namely GABAergic neurons containing a calcium-binding protein parvalbumin, also make reciprocal synapses with mitral/tufted cells in the external plexiform layer. Therefore, neuronal processes making reciprocal synapses with mitral/tufted cells in the external plexiform layer cannot be determined a priori as granule cell processes.
运用包埋前免疫细胞化学技术,在光学显微镜下鉴定大鼠嗅球外丛状层中含有钙结合蛋白小白蛋白的神经元,随后通过电子显微镜连续切片和三维重建技术对其进行分析。在本研究中,我们选取了几种不同类型的小白蛋白免疫反应性神经元,它们在光学显微镜下分别被鉴定为范·格胡滕细胞类型、浅层短轴突细胞类型和多极细胞类型。小白蛋白免疫反应性胞体在超微结构特征上彼此相似,表现为核凹陷、高尔基体适度发达且线粒体丰富;这些结构特征似乎与先前电子显微镜研究中报道的肾小球周围和颗粒细胞层中的短轴突细胞相似。本研究中分析的所有神经元均在假定的二尖瓣/簇状细胞的树突和胞体上形成对称突触,并从它们那里接受不对称突触,偶尔还与它们形成相互突触。在小白蛋白免疫反应性突起上,不对称突触的数量几乎与对称突触相等,其中约30 - 50%被鉴定为相互突触对。相比之下,在小白蛋白免疫反应性胞体上未观察到突触前位点,近端树突的粗大部分(直径超过约2微米)在某些来自小白蛋白免疫阴性轮廓的不对称和对称突触中偶尔作为突触后位点。其特征在于,小白蛋白免疫反应性突起经常相互直接接触;在光学显微镜下被认为起源于胞体或树突或小白蛋白免疫反应性神经元的突起,有时通过电子显微镜检查发现是分开但直接接触的突起。尽管在这些接触位点偶尔观察到粘着斑,但到目前为止既未观察到缝隙连接也未观察到化学突触。到目前为止,人们一直认为在嗅球外丛状层中只有颗粒细胞与二尖瓣/簇状细胞形成相互突触。然而,本研究清楚地表明,不同于颗粒细胞的中间神经元,即含有钙结合蛋白小白蛋白的γ-氨基丁酸能神经元,也在嗅球外丛状层中与二尖瓣/簇状细胞形成相互突触。因此,在嗅球外丛状层中与二尖瓣/簇状细胞形成相互突触的神经元突起不能预先确定为颗粒细胞突起。