Flink R, Westman J
J Comp Neurol. 1986 Aug 15;250(3):265-81. doi: 10.1002/cne.902500302.
A comparative light and electron microscopic study was made of the two major neuron populations in the feline lateral cervical nucleus (LCN) that have an ascending projection--namely, the cervicothalamic and cervicomesencephalic neurons. The small population of neurons in the LCN that remained unlabelled after extensive injections into all known areas of LCN termination was also investigated. The intra-axonal retrograde tracing technique was employed and three different tracers were used: native horseradish peroxidase, horseradish peroxidase conjugated to wheat germ agglutinin, and cholera toxin subunit B (CTb). The diaminobenzidine and tetramethylbenzidine methods were used for the peroxidase reaction, and an immunocytochemical staining method with monoclonal antibodies was employed to localize CTb. The light microscopic cell count was performed on plastic-embedded semithin (2 micron) sections, and a section-embedding technique was used for sampling regions of interest for electron microscopy. The total number of neurons in the LCN was calculated to be 8,300, which is higher than numbers reported from other studies on frozen sections. It was concluded from control experiments that many neurons fail to counterstain in frozen sections. The average proportion of labelled cervicothalamic neurons was 94%, which accords with earlier reports. The frequency of labelled neurons projecting to the midbrain was 25-49%, depending on the method used. The highest number of labelled neurons was found with the immunocytochemical method with use of CTb as a tracer. In the electron microscopic study, the cell area, form factor, nuclear area, bouton covering ratio, mean appositional length of boutons, and bouton density were measured. There were no significant differences in these respects between the cervicothalamic and cervicomesencephalic neurons, but the unlabelled neurons differed significantly from the labelled ones, with a smaller somal area, a lower bouton covering ratio, and a larger relative nuclear area. The ascending neurons were scattered over the entire LCN, but the neurons that remained unlabelled after the extensive injections was found in its ventromedial part. It is suggested that these are interneurons. In the light microscopic study of the animals injected with CTb, the ventromedial part of the LCN displayed labelled structures resembling terminals. Electron microscopic examination of the sections revealed boutons synapsing on unlabelled neurons and dendrites. Occasionally labelled neurons and dendrites were also contacted.(ABSTRACT TRUNCATED AT 400 WORDS)
对猫外侧颈核(LCN)中具有上行投射的两类主要神经元群,即颈丘脑神经元和颈中脑神经元,进行了光镜和电镜比较研究。还对在向LCN所有已知终末区域广泛注射后仍未标记的少量LCN神经元进行了研究。采用轴突内逆行追踪技术,并使用了三种不同的示踪剂:天然辣根过氧化物酶、与麦胚凝集素结合的辣根过氧化物酶以及霍乱毒素B亚单位(CTb)。用二氨基联苯胺和四甲基联苯胺法进行过氧化物酶反应,并用单克隆抗体免疫细胞化学染色法定位CTb。在塑料包埋的半薄(2微米)切片上进行光镜细胞计数,并采用切片包埋技术对感兴趣区域进行电镜取样。计算出LCN中神经元的总数为8300个,这一数字高于其他关于冰冻切片研究报告的数量。从对照实验得出结论,许多神经元在冰冻切片中未能进行复染。标记的颈丘脑神经元的平均比例为94%,这与早期报告一致。投射到中脑的标记神经元的频率为25% - 49%,具体取决于所使用的方法。使用CTb作为示踪剂的免疫细胞化学方法发现的标记神经元数量最多。在电镜研究中,测量了细胞面积、形态因子、核面积、终扣覆盖率、终扣平均贴附长度和终扣密度。在这些方面,颈丘脑神经元和颈中脑神经元之间没有显著差异,但未标记的神经元与标记的神经元有显著差异,其胞体面积较小、终扣覆盖率较低且相对核面积较大。上行神经元散布于整个LCN,但在广泛注射后仍未标记的神经元位于其腹内侧部分。提示这些是中间神经元。在对注射CTb的动物进行的光镜研究中,LCN的腹内侧部分显示出类似终末的标记结构。对切片的电镜检查显示终扣与未标记的神经元和树突形成突触。偶尔也有标记的神经元和树突发生接触。(摘要截断于400字)