Fuller T A, Price J L
Department of Psychiatry, Washington University, School of Medicine, St. Louis, Missouri 63110.
J Comp Neurol. 1988 Oct 8;276(2):209-18. doi: 10.1002/cne.902760205.
The "transmitter-specific" retrograde axonal tracer 3H-D-aspartate has been used to demonstrate neurons in the olfactory bulb which putatively utilize aspartate and/or glutamate as their neurotransmitter and which send an axon either to the piriform cortex or within the bulb itself. Injections of 3H-D-aspartate into layer I of the anterior piriform cortex, in the zone of termination of axons from the olfactory bulb, labeled only a few cells in the main olfactory bulb, located in the mitral and external plexiform layers. Although these cells resembled mitral and tufted cells, they tended to have smaller somata than other mitral or tufted cells and apparently form a distinct subpopulation of relay cells. In contrast, many of the mitral cells of the accessory olfactory bulb were labeled by the same injections of 3H-D-aspartate, probably as a result of involvement of the accessory olfactory tract or its bed nucleus in the injection site. Similar injections of the "nonspecific" tracer HRP into the anterior piriform cortex labeled most of the cells in the mitral cell layer of both the main and accessory olfactory bulbs, and some tufted cells in the external plexiform layer. It is concluded that only a small, distinct subpopulation of the mitral or tufted cells of the main olfactory bulb are aspartatergic and/or glutamatergic, while many (at least) of the mitral cells of the accessory olfactory bulb use the excitatory amino acids as transmitters. Injections of 3H-D-aspartate directly into the main olfactory bulb also failed to label the mitral and deeply situated tufted cells. However, a few cells were labeled in the periglomerular region, the superficial external plexiform layer, and the granule cell layer near the injection site. These labeled cells were smaller than mitral and tufted cells but generally larger than periglomerular or granule cells. They may represent a population of glutamatergic or aspartatergic short axon cells. In addition, small cells of an unknown type were labeled in the olfactory nerve layer following injections in the deepest part of the bulb. These cells do not correspond to any of the well characterized cell types of the olfactory bulb.
“递质特异性”逆行轴突示踪剂³H-D-天冬氨酸已被用于显示嗅球中的神经元,这些神经元可能利用天冬氨酸和/或谷氨酸作为神经递质,并将轴突发送至梨状皮质或嗅球本身内部。将³H-D-天冬氨酸注射到前梨状皮质的I层,即嗅球轴突的终末区域,仅标记了主嗅球中位于二尖瓣层和外丛状层的少数细胞。尽管这些细胞类似于二尖瓣细胞和簇状细胞,但它们的胞体往往比其他二尖瓣细胞或簇状细胞小,显然形成了一个独特的中继细胞亚群。相比之下,副嗅球的许多二尖瓣细胞被相同的³H-D-天冬氨酸注射标记,这可能是由于副嗅束或其床核参与了注射部位。将“非特异性”示踪剂辣根过氧化物酶(HRP)类似地注射到前梨状皮质中,标记了主嗅球和副嗅球二尖瓣细胞层中的大多数细胞,以及外丛状层中的一些簇状细胞。得出的结论是,主嗅球中只有一小部分独特的二尖瓣细胞或簇状细胞是天冬氨酸能和/或谷氨酸能的,而副嗅球的许多(至少)二尖瓣细胞使用兴奋性氨基酸作为递质。将³H-D-天冬氨酸直接注射到主嗅球中也未能标记二尖瓣细胞和位于深部的簇状细胞。然而,在注射部位附近的肾小球周围区域、浅表外丛状层和颗粒细胞层中标记了一些细胞。这些标记细胞比二尖瓣细胞和簇状细胞小,但通常比肾小球周围细胞或颗粒细胞大。它们可能代表一群谷氨酸能或天冬氨酸能的短轴突细胞。此外,在嗅球最深部注射后,嗅神经层中标记了未知类型的小细胞。这些细胞与嗅球中任何特征明确的细胞类型都不对应。