Kosaka T, Deans M R, Paul D L, Kosaka K
Department of Anatomy and Neurobiology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.
Neuroscience. 2005;134(3):757-69. doi: 10.1016/j.neuroscience.2005.04.057.
In the present study we analyzed the structural features of extraglomerular gap junction-forming processes in mouse olfactory bulb electron microscopically. This work complements a previous study in which we analyzed the structural features of neuronal gap junction-forming processes within the glomerulus itself. Furthermore we examined connexin 36 expressing cells in the mouse olfactory bulb by analyzing transgenic mice in which the connexin 36 coding sequence was replaced with histological reporters. In extraglomerular regions, the mitral/tufted cell somata, dendrites and axon hillocks made gap junctions and mixed synapses with interneuronal processes. These gap junctions and synapses were associated with various types of interneuronal processes, including a particular type of sheet-like or calyx-like process contacting the somata or large dendrites of mitral/tufted cells. In the olfactory bulbs of the transgenic mice, connexin 36 was expressed in mitral cells, tufted cells, presumed granule cells and periglomerular cells. Multiple immunofluorescent labelings further revealed that presumed interneurons expressing connexin 36 in the periglomerular region rarely expressed calbindin, calretinin or tyrosine hydroxylase and are likely to comprise a chemically uncharacterized class of neurons. Similarly, interneurons expressing connexin 36 in the granule cell layer were rarely positive for calretinin, which was expressed in numerous presumed granule cells in the mouse main olfactory bulb. In summary, these findings revealed that mitral/tufted cells make gap junctions with diverse types of neurons; in the glomeruli gap junction-forming interneuronal processes originated from some types of periglomerular cells but others from a hitherto uncharacterized neuron type(s), and in the extraglomerular region gap-junction forming processes originate mainly from a subset of cells within the granule cell layer.
在本研究中,我们通过电子显微镜分析了小鼠嗅球中形成球外间隙连接的突起的结构特征。这项工作补充了之前的一项研究,在那项研究中我们分析了肾小球内形成神经元间隙连接的突起的结构特征。此外,我们通过分析转基因小鼠来检测小鼠嗅球中表达连接蛋白36的细胞,在这些转基因小鼠中,连接蛋白36的编码序列被组织学报告基因所取代。在球外区域,二尖瓣/簇状细胞的胞体、树突和轴丘与中间神经元的突起形成了间隙连接和混合突触。这些间隙连接和突触与各种类型的中间神经元突起相关,包括一种特殊类型的片状或花萼状突起,它们接触二尖瓣/簇状细胞的胞体或大树突。在转基因小鼠的嗅球中,连接蛋白36在二尖瓣细胞、簇状细胞、推测的颗粒细胞和球周细胞中表达。多重免疫荧光标记进一步显示,在球周区域表达连接蛋白36的推测中间神经元很少表达钙结合蛋白、钙视网膜蛋白或酪氨酸羟化酶,并且可能构成一类化学性质未明确的神经元。同样,在颗粒细胞层中表达连接蛋白36的中间神经元很少对钙视网膜蛋白呈阳性,而钙视网膜蛋白在小鼠主嗅球中的许多推测颗粒细胞中表达。总之,这些发现表明二尖瓣/簇状细胞与多种类型的神经元形成间隙连接;在肾小球中,形成间隙连接的中间神经元突起起源于某些类型的球周细胞,但其他突起则来自迄今未明确的神经元类型,而在球外区域,形成间隙连接的突起主要起源于颗粒细胞层内的一部分细胞。