Ott Swidbert R, Elphick Maurice R
School of Biological Sciences, Queen Mary, University of London, Mile End Road, London E1 4NS, United Kingdom.
J Comp Neurol. 2002 Jun 24;448(2):165-85. doi: 10.1002/cne.10235.
Formaldehyde-insensitive NADPH diaphorase (NADPHd) activity is used widely as a histochemical marker for neuronal nitric oxide synthase (NOS). However, in several insects including the cockroach Periplaneta americana, NOS is apparently formaldehyde-sensitive; NADPHd fails to reveal neuron morphology and results in faint generalized staining. Here we have used a novel fixative, methanol/ formalin (MF), to reveal for the first time the neuroarchitecture of NADPHd in the cockroach, with intense selective staining occurring in neurons throughout the brain and thoracic ganglia. Immunocytochemical and histochemical analysis of cockroach and locust nervous systems indicated that neuronal NADPHd after MF fixation can be attributed to NOS. However, NADPHd in locust glial and perineurial cells was histochemically different from that in neurons and may thus be due to enzymes other than NOS. Histochemical implications of species-specific enzyme properties and of the transcriptional complexity of the NOS gene are discussed. The present findings suggest that MF fixation is a valuable new tool for the comparative analysis of the neuroarchitecture of NO signaling in insects. The Golgi-like definition of the staining enabled analysis of the NADPHd architecture in the cockroach and comparison with that in the locust. NADPHd in the tactile neuropils of the thoracic ganglia showed a similar organization in the two species. The olfactory glomeruli of the antennal lobes were in both species densely innervated by NADPHd-positive local interneurons that correlated in number with the number of glomeruli. Thus, the NADPHd architectures appear highly conserved in primary sensory neuropils. In the cockroach mushroom bodies, particularly dense staining in the gamma-layer of the lobes was apparently derived from Kenyon cells, whereas extrinsic arborizations were organized in domains across the lobes, an architecture that contrasts with the previously described tubular compartmentalization of locust mushroom bodies. These divergent architectures may result in different spatiotemporal dynamics of NO diffusion and suggest species differences in the role of NO in the mushroom bodies.
对甲醛不敏感的烟酰胺腺嘌呤二核苷酸磷酸黄递酶(NADPHd)活性被广泛用作神经元型一氧化氮合酶(NOS)的组织化学标记物。然而,在包括美洲大蠊在内的几种昆虫中,NOS显然对甲醛敏感;NADPHd无法显示神经元形态,只会产生微弱的弥漫性染色。在这里,我们使用了一种新型固定剂甲醇/福尔马林(MF),首次揭示了蟑螂中NADPHd的神经结构,在整个大脑和胸神经节的神经元中出现了强烈的选择性染色。对蟑螂和蝗虫神经系统的免疫细胞化学和组织化学分析表明,MF固定后的神经元NADPHd可归因于NOS。然而,蝗虫神经胶质细胞和神经周细胞中的NADPHd在组织化学上与神经元中的不同,因此可能是由NOS以外的酶引起的。讨论了物种特异性酶特性和NOS基因转录复杂性的组织化学意义。目前的研究结果表明,MF固定是一种有价值的新工具,可用于昆虫中NO信号神经结构的比较分析。染色的高尔基体样清晰度使得能够分析蟑螂中的NADPHd结构并与蝗虫中的进行比较。胸神经节触觉神经纤维中的NADPHd在这两个物种中显示出相似的组织方式。触角叶的嗅觉小球在两个物种中都被NADPHd阳性的局部中间神经元密集支配,其数量与小球数量相关。因此,NADPHd结构在初级感觉神经纤维中似乎高度保守。在蟑螂的蘑菇体中,叶γ层中特别密集的染色显然来自肯扬细胞,而外部分支则在叶间区域组织,这种结构与先前描述的蝗虫蘑菇体的管状分隔形成对比。这些不同的结构可能导致NO扩散的时空动态不同,并表明NO在蘑菇体中的作用存在物种差异。