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氧化对苯二胺:环氧包埋组织中染色反应的观察

Oxidized p-phenylenediamine: observations on the staining reaction in epoxy embedded tissues.

作者信息

Armas-Portela R, Stockert J C, Ferrer J M, Tato A, Gómez-Perretta C, Callaghan R C

出版信息

Acta Histochem Suppl. 1986;32:255-66.

PMID:2422692
Abstract

p-Phenylenediamine (PPD) is easily oxidized to brown compounds which stain acidic substrates. On account of the spontaneous oxidation process, the colour of PPD increases and becomes ochre-brown in a few days, showing an absorption peak at lambda = 510 nm with shoulder at about 440 to 460 nm. Studies on the application of oxidized PPD as a stain for semi-thin sections revealed that some tissue components could be clearly visualized. After glutaraldehyde fixation, semi-thin and thin sections of animal tissues were treated with 0.5% aqueous PPD solutions which were aged for variable times at room temperature. Microvilli, goblet cell mucin, mast cell granules, cartilage matrix, collagen, elastin, keratohyalin granules, acrosomes, cytoplasmic granules of Drosophila hydei salivary glands and chromatin showed positive staining reactions after treatment of semi-thin sections with oxidized PPD (7-10 days aged) for 20-30 minutes. Microspectrophotometric studies revealed an absorption peak at lambda = 520-530 nm and a shoulder at lambda = 440-460 nm in goblet cell mucin stained by oxidized PPD. In the presence of anionic macromolecules, the main peak of oxidized PPD solutions showed a strong hyperchromism. Thin sections stained by oxidized PPD did not appear contrasted, but the treatment with 0.125% gold chloride (AuCl3) induced massive gold deposits in structures stained by oxidized PPD. Hyperchromic shifts were also produced in oxidized PPD solutions after the addition of small amounts of AuCl3. This procedure can be used as a simple and rapid staining method for epoxy sections, giving selective contrast for some tissue components.

摘要

对苯二胺(PPD)很容易被氧化成棕色化合物,这些化合物会使酸性底物染色。由于自发氧化过程,PPD的颜色会加深,并在几天内变成赭褐色,在λ = 510 nm处出现吸收峰,在约440至460 nm处有肩峰。对氧化PPD作为半薄切片染色剂的应用研究表明,一些组织成分可以清晰地显现出来。用戊二醛固定后,动物组织的半薄切片和超薄切片用0.5%的PPD水溶液处理,该溶液在室温下放置不同时间进行老化。用氧化PPD(老化7 - 10天)处理半薄切片20 - 30分钟后,微绒毛、杯状细胞粘蛋白、肥大细胞颗粒、软骨基质、胶原蛋白、弹性蛋白、透明角质颗粒、顶体、海德氏果蝇唾液腺的细胞质颗粒和染色质呈现阳性染色反应。显微分光光度研究表明,氧化PPD染色的杯状细胞粘蛋白在λ = 520 - 530 nm处有吸收峰,在λ = 440 - 460 nm处有肩峰。在阴离子大分子存在的情况下,氧化PPD溶液的主峰呈现强烈的增色效应。氧化PPD染色的超薄切片没有出现反差,但用0.125%的氯化金(AuCl3)处理后,在氧化PPD染色的结构中诱导产生大量金沉积。加入少量AuCl3后,氧化PPD溶液也会产生增色位移。该方法可作为环氧树脂切片的一种简单快速的染色方法,对一些组织成分产生选择性反差。

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