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用于光学和电子显微镜检查的预固定脑组织中密集的辣根过氧化物酶填充。

Dense HRP filling in pre-fixed brain tissue for light and electron microscopy.

作者信息

Kageyama G H, Meyer R L

出版信息

J Histochem Cytochem. 1987 Oct;35(10):1127-36. doi: 10.1177/35.10.3624853.

Abstract

The use of neuroanatomical markers in tissues that have been pre-fixed has been virtually ignored, even though this approach could offer certain advantages over in vivo methods, in terms of convenience of application and choice of markers. We have found that HRP can be used on well-fixed brains of cats and goldfish to fill neurons, dendrites, axons, terminals, glial cells, and glial processes for high-resolution light microscopy and electron microscopy. Best results were obtained using brains that were perfusion-fixed with 2.5% depolymerized paraformaldehyde and 1.5% glutaraldehyde. Two methods of HRP application were used: optically guided injections of microliter quantities into various regions of cat brain, and optic nerve fills in goldfish by attaching an HRP-filled polyethylene tube for periods of 1 day to 2 weeks. HRP applied in these ways to pre-fixed tissue was found to fill neurons or glial cells with solid label in the anterograde and retrograde directions.

摘要

在预先固定的组织中使用神经解剖学标记实际上一直被忽视,尽管就应用的便利性和标记物的选择而言,这种方法可能比体内方法具有某些优势。我们发现,辣根过氧化物酶(HRP)可用于猫和金鱼固定良好的大脑,以填充神经元、树突、轴突、终末、神经胶质细胞和神经胶质突起,用于高分辨率光学显微镜和电子显微镜观察。使用用2.5%解聚多聚甲醛和1.5%戊二醛进行灌注固定的大脑可获得最佳结果。采用了两种HRP应用方法:在光学引导下将微升量的HRP注射到猫脑的各个区域,以及通过将充满HRP的聚乙烯管连接1天至2周对金鱼进行视神经填充。发现以这些方式应用于预先固定组织的HRP可在顺行和逆行方向用固体标记物填充神经元或神经胶质细胞。

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