Morita Y, Finger T E
Department of Cellular and Structural Biology, Rocky Mountain Taste and Smell Center, University of Colorado School of Medicine, Denver 80262, USA.
J Comp Neurol. 1998 Sep 7;398(4):539-50. doi: 10.1002/(sici)1096-9861(19980907)398:4<539::aid-cne6>3.0.co;2-3.
The primary olfactory projections of channel catfish Ictalurus punctatus have been examined with postmortem tracing by using either 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate or 1,1-dilinoleyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI). Following DiI deposition into small areas in different parts of the posterior olfactory bulb, olfactory sensory neurons always were labeled throughout the olfactory epithelium. No obvious topographical mapping exists between the epithelium and olfactory bulb. The different dye placements, however, did result in labeling of different morphologies of receptor cells, depending on the site of injection. Retrogradely labeled neurons in the olfactory epithelium were classified into three types on the basis of their height: tall, intermediate, and short. Tall olfactory sensory neurons had perikarya at the bottom one-fourth of the epithelium, extended slender dendrites to the epithelial surface, and possessed numerous cilia on the apical dendritic tips. These tall olfactory sensory neurons were labeled predominantly following DiI applications to the ventral part of the posterior olfactory bulb. In contrast, the short olfactory sensory neurons had perikarya situated within the superficial half of the epithelium and with short apical dendrites bearing microvilli. These short olfactory sensory neurons projected predominantly to the dorsal, posterior olfactory bulb. Thus, short microvillous receptor cells and tall ciliated receptor cells connect to different parts of the olfactory bulb, although the receptor cells are intermingled within the olfactory epithelium. Because different parts of the olfactory bulb are thought to respond preferentially to different classes of odorants, these results suggest that receptor cell morphology may be related to odorant quality detection. In addition, to compare this study with previous in vivo studies, Fluoro-Gold was injected in vivo into either the olfactory bulb or intraperitoneally. These in vivo studies show that so-called "type II ciliar receptor cells" of the nonsensory epithelium are labeled nonselectively by blood-borne substances, but they are not labeled by postmortem injections of DiI anywhere in the olfactory bulb.
利用1,1'-二辛基-3,3,3',3'-四甲基吲哚羰花青高氯酸盐或1,1-二亚油酰基-3,3,3',3'-四甲基吲哚羰花青高氯酸盐(DiI),通过死后追踪法对斑点叉尾鮰的初级嗅觉投射进行了研究。将DiI注入后嗅球不同部位的小区域后,嗅觉感觉神经元始终在整个嗅觉上皮中被标记。上皮和嗅球之间不存在明显的拓扑映射。然而,根据注射部位的不同,不同的染料注入确实导致了不同形态的受体细胞被标记。嗅觉上皮中逆行标记的神经元根据其高度可分为三种类型:高、中、矮。高嗅觉感觉神经元的胞体位于上皮底部的四分之一处,细长的树突延伸至上皮表面,顶端树突末梢有许多纤毛。这些高嗅觉感觉神经元主要在将DiI应用于后嗅球腹侧部分后被标记。相比之下,矮嗅觉感觉神经元的胞体位于上皮的浅表一半内,顶端短树突带有微绒毛。这些矮嗅觉感觉神经元主要投射到背侧、后嗅球。因此,短微绒毛受体细胞和高纤毛受体细胞连接到嗅球的不同部位,尽管受体细胞在嗅觉上皮内相互交织。由于嗅球的不同部分被认为对不同类别的气味剂有优先反应,这些结果表明受体细胞形态可能与气味剂质量检测有关。此外,为了将本研究与以前的体内研究进行比较,将荧光金体内注入嗅球或腹腔内。这些体内研究表明,非感觉上皮的所谓“II型纤毛受体细胞”被血源性物质非选择性地标记,但在嗅球的任何部位进行死后DiI注射时它们都不会被标记。