Nance D M, Burns J
Department of Anatomy, Faculty of Medicine, Dalhousie University Halifax, Nova Scotia, Canada.
Brain Res Bull. 1990 Jul;25(1):139-45. doi: 10.1016/0361-9230(90)90264-z.
We have examined five conjugated 10,000 mol. wt. dextrans as potential anterograde tract tracers: Lucifer Yellow, Texas Red, fluorescein, Cascade Blue and tetramethylrhodamine. Pressure injections were made into the brain, dorsal root ganglia or footpads of adult rats. The retrograde tracer Fluoro-Gold was injected alone or mixed with the dextrans before injection. Three-14 days after injection, animals were perfused and sections cut with a freezing microtome. Texas Red-, fluorescein- and tetramethylrhodamine-conjugated dextrans produced intense labeling of neuronal cell bodies, axons and dendritic processes at the injection site and were transported by neurons predominantly in an anterograde direction to yield terminal and preterminal labeling. Relative to the fluorescein and tetramethylrhodamine conjugates, the quality and intensity of the anterograde labeling produced by Texas Red was variable. Results with Lucifer Yellow and Cascade Blue conjugates were negative. Optimal results were produced by slow-pressure injections via glass micropipettes. In comparison with Fluoro-Gold, retrograde transport by the dextran conjugates was present, but limited in its extent. Injections of the tetramethylrhodamine conjugate into dorsal root ganglia produced anterograde labeling of afferent fibers in visceral organs and injections into the nucleus ambiguous labeled motor fibers in the esophagus. Double/triple labeling was observed in the brain and spinal cord following multiple injections of fluorescein, tetramethylrhodamine and Fluoro-Gold. Also, Fluoro-Gold could be mixed with one of the dextrans in order to produce specific retrograde and anterograde labeling from the same injection site. The conjugates were compatible with fluorescent immunocytochemical procedures, but proved unsuitable for peripheral injections.(ABSTRACT TRUNCATED AT 250 WORDS)
我们检测了5种共轭10,000分子量葡聚糖作为潜在的顺行束路示踪剂:路西法黄、德克萨斯红、荧光素、级联蓝和四甲基罗丹明。向成年大鼠的脑、背根神经节或足垫进行压力注射。逆行示踪剂氟金在注射前单独注射或与葡聚糖混合注射。注射后3 - 14天,对动物进行灌注,并用冷冻切片机切片。德克萨斯红、荧光素和四甲基罗丹明共轭葡聚糖在注射部位对神经元细胞体、轴突和树突过程产生强烈标记,并主要由神经元沿顺行方向运输,产生终末和终末前标记。相对于荧光素和四甲基罗丹明共轭物,德克萨斯红产生的顺行标记的质量和强度是可变的。路西法黄和级联蓝共轭物的结果为阴性。通过玻璃微吸管进行缓慢压力注射可产生最佳结果。与氟金相比,葡聚糖共轭物存在逆行运输,但其范围有限。将四甲基罗丹明共轭物注射到背根神经节可产生内脏器官传入纤维的顺行标记,注射到疑核可标记食管中的运动纤维。多次注射荧光素、四甲基罗丹明和氟金后,在脑和脊髓中观察到双标记/三标记。此外,氟金可与其中一种葡聚糖混合,以便从同一注射部位产生特定的逆行和顺行标记。这些共轭物与荧光免疫细胞化学程序兼容,但被证明不适合外周注射。(摘要截断于250字)