Johansson O, Backman J
J Neurosci Methods. 1983 Feb;7(2):185-93. doi: 10.1016/0165-0270(83)90081-x.
A modification of the peroxidase-antiperoxidase immunohistochemical method involving the use of OsO4 for the visualization of antigens in tissue using thick sections is described. This modification has lead to consistent enhancement of the intensity of the reaction product and thus to a further amplification of sensitivity in this particular system. The present procedure results in a sensitive demonstration of neuronal antigens such as peptides and synthesizing enzymes in neurons. The method allows the investigator to analyze the cytoarchitecture and geometry of these neurons and their projections in the nervous system as well as more easily detect single, weakly stained nerve fibers. In 50 micrometers sections, immunopositive processes can be followed over long distances. In the present study, the catecholamine-synthesizing enzyme, phenylethanolamine-N-methyltransferase (PNMT), and the neuropeptide, somatostatin, have been used as examples from the central nervous system of the rat, but the procedure is applicable to other antigens as well as other cell types and tissues.
描述了一种过氧化物酶-抗过氧化物酶免疫组织化学方法的改进,该方法涉及使用四氧化锇在厚切片的组织中可视化抗原。这种改进导致反应产物强度的持续增强,从而在这个特定系统中进一步提高了灵敏度。目前的方法能够灵敏地显示神经元抗原,如神经元中的肽和合成酶。该方法使研究者能够分析这些神经元的细胞结构和几何形状及其在神经系统中的投射,并且更容易检测到单个的、弱染色的神经纤维。在50微米厚的切片中,可以追踪免疫阳性的突起很长一段距离。在本研究中,以大鼠中枢神经系统中的儿茶酚胺合成酶苯乙醇胺-N-甲基转移酶(PNMT)和神经肽生长抑素为例,但该方法也适用于其他抗原以及其他细胞类型和组织。