Ultrastructural localization of connexins (Cx36, Cx43, Cx45), glutamate receptors and aquaporin-4 in rodent olfactory mucosa, olfactory nerve and olfactory bulb.

Journal of Neurocytology Pub Date : 2005-09-01 Epub Date: 2006-07-13 DOI:10.1007/s11068-005-8360-2
John E Rash, Kimberly G V Davidson, Naomi Kamasawa, Thomas Yasumura, Masami Kamasawa, Chunbo Zhang, Robin Michaels, Diego Restrepo, Ole P Ottersen, Carl O Olson, James I Nagy
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引用次数: 98

Abstract

Odorant/receptor binding and initial olfactory information processing occurs in olfactory receptor neurons (ORNs) within the olfactory epithelium. Subsequent information coding involves high-frequency spike synchronization of paired mitral/tufted cell dendrites within olfactory bulb (OB) glomeruli via positive feedback between glutamate receptors and closely-associated gap junctions. With mRNA for connexins Cx36, Cx43 and Cx45 detected within ORN somata and Cx36 and Cx43 proteins reported in ORN somata and axons, abundant gap junctions were proposed to couple ORNs. We used freeze-fracture replica immunogold labeling (FRIL) and confocal immunofluorescence microscopy to examine Cx36, Cx43 and Cx45 protein in gap junctions in olfactory mucosa, olfactory nerve and OB in adult rats and mice and early postnatal rats. In olfactory mucosa, Cx43 was detected in gap junctions between virtually all intrinsic cell types except ORNs and basal cells; whereas Cx45 was restricted to gap junctions in sustentacular cells. ORN axons contained neither gap junctions nor any of the three connexins. In OB, Cx43 was detected in homologous gap junctions between almost all cell types except neurons and oligodendrocytes. Cx36 and, less abundantly, Cx45 were present in neuronal gap junctions, primarily at "mixed" glutamatergic/electrical synapses between presumptive mitral/tufted cell dendrites. Genomic analysis revealed multiple miRNA (micro interfering RNA) binding sequences in 3'-untranslated regions of Cx36, Cx43 and Cx45 genes, consistent with cell-type-specific post-transcriptional regulation of connexin synthesis. Our data confirm absence of gap junctions between ORNs, and support Cx36- and Cx45-containing gap junctions at glutamatergic mixed synapses between mitral/tufted cells as contributing to higher-order information coding within OB glomeruli.

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啮齿动物嗅粘膜、嗅神经和嗅球中连接蛋白(Cx36、Cx43、Cx45)、谷氨酸受体和水蒸素-4的超微结构定位。
气味/受体结合和最初的嗅觉信息处理发生在嗅上皮细胞内的嗅受体神经元(ORN)中。随后的信息编码涉及通过谷氨酸受体和密切相关的缝隙连接之间的正反馈,使嗅球(OB)内成对的有簇/无簇细胞树突进行高频尖峰同步。在ORN体节中检测到了连接蛋白Cx36、Cx43和Cx45的mRNA,在ORN体节和轴突中也有Cx36和Cx43蛋白的报道,因此认为有大量的间隙连接将ORN连接起来。我们使用冻裂复制免疫金标记(FRIL)和共聚焦免疫荧光显微镜检测了成年大鼠、小鼠和出生后早期大鼠的嗅粘膜、嗅神经和OB中间隙连接的Cx36、Cx43和Cx45蛋白。在嗅粘膜中,几乎所有固有细胞类型(ORN 和基底细胞除外)之间的间隙连接中都检测到了 Cx43;而 Cx45 则仅限于固有细胞的间隙连接。ORN轴突既不包含间隙连接,也不包含这三种连接蛋白中的任何一种。在OB中,除神经元和少突胶质细胞外,几乎所有细胞类型之间的同源间隙连接中都检测到了Cx43。神经元间隙连接中存在 Cx36,Cx45 的含量较少,主要存在于假定的有丝分裂/簇细胞树突之间的 "混合 "谷氨酸能/电突触。基因组分析显示,在 Cx36、Cx43 和 Cx45 基因的 3'-非翻译区存在多个 miRNA(微干扰 RNA)结合序列,这与细胞类型特异性转录后对连接蛋白合成的调控是一致的。我们的数据证实了ORN之间不存在间隙连接,并支持在有丝分裂/簇细胞之间的谷氨酸能混合突触中含有Cx36和Cx45的间隙连接有助于OB肾小球内的高阶信息编码。
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