Freire M
Instituto Cajal, Madrid, Spain.
J Neurosci Methods. 1990 Dec;35(3):267-75. doi: 10.1016/0165-0270(90)90133-z.
Visually-guided introduction of HRP into perfusion-fixed hamster brain slabs was carried out by three procedures: pressure or extracellular iontophoretic injections, introduction of a small HRP-crystal on the closed tip of a micropipette, and by dropping a very small drop of HRP solution on the ventricular surface. The prefixation was made with a solution of 1% paraformaldehyde and 1% glutaraldehyde in 0.1 M phosphate buffer in time periods ranging from 4 to 26 days. The introduction of HRP-crystals into brain slabs did not produce HRP-filling of cells and processes, but only a granular background of HRP diffusion. Injections into adjacent brain slabs of an HRP-containing solution did produce, in every case, some degree of labelling of neuronal somata, dendrites, individual axons, and fibre bundles. Several cells showed dense HRP-filling of the soma and processes, including dendritic spines and axonal varicosities. Dense HRP-filled axonal terminal arbors were seen in the dorsal lateral geniculate nucleus (dLGN) and superior colliculus (SC) after iontophoretic injections in the optic tract. The good ultrastructural preservation achieved by perfusion of the fixative solution was not affected by the subsequent injection procedures, and the pre- and post-synaptic specializations of HRP-filled axons were recognizable. This approach may prove to be useful in correlative light and electron microscope studies of the synaptic relationships between HRP-filled neurons and axons.
通过三种方法将辣根过氧化物酶(HRP)视觉引导注入灌注固定的仓鼠脑片:压力或细胞外离子电渗注射、在微吸管封闭尖端放置一小颗HRP晶体以及在脑室表面滴一小滴HRP溶液。预固定采用1%多聚甲醛和1%戊二醛溶于0.1 M磷酸盐缓冲液的溶液,时间为4至26天。将HRP晶体引入脑片并未使细胞和突起充满HRP,仅产生HRP扩散的颗粒状背景。向相邻脑片注射含HRP溶液在每种情况下都确实使神经元胞体、树突、单个轴突和纤维束有一定程度的标记。一些细胞的胞体和突起,包括树突棘和轴突膨体,显示出密集的HRP填充。在视束进行离子电渗注射后,在背外侧膝状体核(dLGN)和上丘(SC)可见密集的HRP填充轴突终末分支。固定液灌注所实现的良好超微结构保存不受后续注射程序的影响,并且可识别HRP填充轴突的突触前和突触后特化。这种方法可能在对HRP填充的神经元和轴突之间突触关系的相关光镜和电镜研究中有用。