Holmqvist B I, Ostholm T, Ekström P
Department of Zoology, University of Lund, Sweden.
J Neurosci Methods. 1992 Apr;42(1-2):45-63. doi: 10.1016/0165-0270(92)90134-y.
An important goal in neuroanatomical research is to identify the neurotransmitters in specific neural pathways. One step towards this goal is to combine experimental neuronal tracing with immunocytochemistry. Unfortunately, optimal procedures for nerve tracing and immunocytochemistry are not always compatible. Carbocyanine compounds have recently been shown to be efficient tracers both in vivo and in paraformaldehyde-prefixed neural tissue. The possibility to apply them to prefixed tissue make them suitable for tracing of neural pathways that are not easily accessible in vivo. We have optimized the procedures for neural tracing with one carbocyanine compound, DiI (1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate), in the CNS of a teleost fish, and evaluated its compatibility with different immunocytochemical protocols. We have compared several immunocytochemical protocols, taking into account cryostat and vibratome sectioning, glutaraldehyde post-fixation to stabilize DiI, antibodies with different capacity for tissue penetration and the use of detergents, and antibodies with different sensitivity to prolonged paraformaldehyde fixation. We have also evaluated the choice of marker for immunoreactivity and compared indirect immunofluorescence techniques using different fluorophores, and the peroxidase-antiperoxidase (PAP) technique with or without nickel enhancement of the diaminobenzidine reaction product. It appears that DiI tracing of neural connections in the teleost CNS yields very consistent results and that the combination with immunocytochemistry is very reliable. We present four different basic protocols for combined DiI tracing and immunocytochemistry, with notes on their specific applicability. Owing to their reliability, the protocols may prove useful in comparative neuroanatomical studies of other vertebrates, particularly fish and amphibians, as well as in studies of developmental changes and neural plasticity in fish and amphibians.
神经解剖学研究的一个重要目标是确定特定神经通路中的神经递质。实现这一目标的一个步骤是将实验性神经元追踪与免疫细胞化学相结合。不幸的是,神经追踪和免疫细胞化学的最佳程序并不总是兼容的。最近已证明,花青化合物在体内和多聚甲醛预固定的神经组织中都是有效的示踪剂。将它们应用于预固定组织的可能性使其适用于追踪体内不易触及的神经通路。我们优化了用一种花青化合物DiI(1,1'-二辛基-3,3,3',3'-四甲基吲哚羰花青高氯酸盐)在硬骨鱼中枢神经系统中进行神经追踪的程序,并评估了其与不同免疫细胞化学方案的兼容性。我们比较了几种免疫细胞化学方案,考虑了冰冻切片机和振动切片机切片、戊二醛后固定以稳定DiI、具有不同组织穿透能力的抗体和去污剂的使用,以及对长时间多聚甲醛固定具有不同敏感性的抗体。我们还评估了免疫反应性标记物的选择,并比较了使用不同荧光团的间接免疫荧光技术,以及有无镍增强二氨基联苯胺反应产物的过氧化物酶-抗过氧化物酶(PAP)技术。看来,硬骨鱼中枢神经系统中DiI对神经连接的追踪产生了非常一致的结果,并且与免疫细胞化学的结合非常可靠。我们提出了四种不同的DiI追踪和免疫细胞化学联合的基本方案,并注明了它们的具体适用性。由于其可靠性,这些方案可能在其他脊椎动物,特别是鱼类和两栖类的比较神经解剖学研究中有用,以及在鱼类和两栖类的发育变化和神经可塑性研究中有用。