van den Pol A N
Neuroscience. 1986 Mar;17(3):643-59. doi: 10.1016/0306-4522(86)90037-0.
An ultrastructural immunocytochemical study was undertaken to identify neuroactive substances contained in presynaptic boutons in the hypothalamic suprachiasmatic nucleus. Axonal boutons containing immunoreactive gamma-aminobutyrate, glutamate decarboxylase, neurophysin/vasopressin, gastrin releasing peptide/bombesin, somatostatin and serotonin were localized within the hypothalamic suprachiasmatic nucleus with pre-embedding peroxidase immunostaining. Synaptic contacts were found between boutons containing each of these substances and postsynaptic structures. While some variation in synaptic morphology existed, most of the immunoreactive contacts were of the symmetrical type. Previous work has indicated that neuroactive peptides may be found in highest concentrations in dense-core vesicles, to examine the subcellular localization of the amino acid inhibitory transmitter gamma-aminobutyrate, ultrastructural immunocytochemistry with pre-embedding peroxidase was compared with post-embedding immunocytochemistry with colloidal gold. Ultracryothin sections were also used for ultrastructural localization of gamma-aminobutyrate and glutamate decarboxylase immunoreactivity. Both gamma-aminobutyrate and glutamate decarboxylase immunoreactivity were found throughout the cytoplasm of immunoreactive boutons when pre-embedding peroxidase was used; with post-embedding colloidal gold immunostaining, label was found over areas containing small clear vesicles, and over mitochondria of immunoreactive axons. At the dilutions used in this study, strongly immunoreactive gamma-aminobutyrate dendrites, boutons forming asymmetrical synapses, and cell bodies were not found. Differences between pre-embedding and post-embedding immunostaining may be due to antigen and label diffusion caused by mild fixation and membrane damage necessary for antisera penetration during pre-embedding immunostaining. These results suggest that gamma-aminobutyrate, gastrin releasing peptide, somatostatin and vasopressin are contained in axons making contact with neurons of the suprachiasmatic nucleus, and may function as neurotransmitters here. Since all of these substances can also be localized in perikarya within the suprachiasmatic nucleus, there is a strong possibility that at least some of the axons containing immunoreactivity for each of these substances may be involved in local circuit interactions between neurons within the suprachiasmatic nucleus.
开展了一项超微结构免疫细胞化学研究,以鉴定下丘脑视交叉上核中突触前终扣所含的神经活性物质。采用包埋前过氧化物酶免疫染色法,在视交叉上核内定位了含有免疫反应性γ-氨基丁酸、谷氨酸脱羧酶、神经垂体素/加压素、胃泌素释放肽/蛙皮素、生长抑素和5-羟色胺的轴突终扣。发现含有这些物质的终扣与突触后结构之间存在突触联系。虽然突触形态存在一些差异,但大多数免疫反应性突触联系属于对称型。先前的研究表明,神经活性肽可能在致密核心囊泡中浓度最高,为了研究氨基酸抑制性递质γ-氨基丁酸的亚细胞定位,将包埋前过氧化物酶超微结构免疫细胞化学与胶体金包埋后免疫细胞化学进行了比较。超薄冷冻切片也用于γ-氨基丁酸和谷氨酸脱羧酶免疫反应性的超微结构定位。使用包埋前过氧化物酶时,在免疫反应性终扣的整个细胞质中都发现了γ-氨基丁酸和谷氨酸脱羧酶免疫反应性;采用包埋后胶体金免疫染色时,在含有小清亮囊泡的区域以及免疫反应性轴突中的线粒体上发现了标记。在本研究使用的稀释度下,未发现强免疫反应性的γ-氨基丁酸树突、形成不对称突触的终扣和细胞体。包埋前和包埋后免疫染色的差异可能是由于包埋前免疫染色期间轻度固定和抗血清穿透所需的膜损伤导致的抗原和标记扩散。这些结果表明,γ-氨基丁酸、胃泌素释放肽、生长抑素和加压素存在于与视交叉上核神经元接触的轴突中,并可能在此处作为神经递质发挥作用。由于所有这些物质也可定位在视交叉上核内的神经元胞体中,因此极有可能至少一些含有这些物质免疫反应性的轴突参与视交叉上核内神经元之间的局部回路相互作用。