Kiernan J A
J Microsc. 1984 Apr;134(Pt 1):25-39. doi: 10.1111/j.1365-2818.1984.tb00501.x.
The staining properties of chromoxane cyanine R (Colour Index No. 43820, Mordant blue 3; also known as eriochrome cyanine R and solochrome cyanine R) have been studied. Used alone, the dye imparted its red colour to nuclei, cytoplasm and collagen. The dye was extracted by mild alkali but not by acids. Stainability required ionized amino groups in the tissue, and there was also evidence for non-ionic binding of the dye. The colours obtained by staining with mixtures of chromoxane cyanine R and ferric chloride varied with the molar iron:dye ratio and with the pH. Useful staining was seen only between pH 1 and 2. The tissues were coloured either all blue (when Fe:dye was high), or both red and blue (when Fe:dye was low). Lower pH favoured the deposition of red, higher pH the deposition of blue colour. The red was mainly in cytoplasm, blue in nuclei and myelin. Collagen fibres were red or purple, depending on pH and iron:dye ratio. Red colours were differentiated by acid and changed to blue, but not extracted, by mild alkali. The red substance in the stained sections was clearly not the free dye, so it was probably an iron-dye complex. From the effects of various differentiating agents, it was deduced that the red and blue dye-metal complex molecules were bound to the tissue by the dye moiety, not by interposition of iron atoms. Staining by the complexes of iron(III) with chromoxane cyanine R did not involve nucleic acids or other polyanions or the amino groups of proteins. There was evidence for only non-ionic binding of both red and blue complexes. It is suggested that the red colour in sections stained by solutions with low iron:dye ratio is due to a simple carboxylate complex, [ Fe2H (dye)]-. The blue colour would then result from withdrawal of a proton from the red complex to give [Fe2(dye)]2-. The bases that remove the protons may be arginine-rich nucleoproteins of nuclei and phospholipid bases of myelin. Techniques are described for informative simultaneous staining in two colours, and for the selective staining of either nuclei or myelin.
对铬变青R(《染料索引》编号43820,媒染蓝3;也称为依来铬氰蓝R和溶剂铬氰蓝R)的染色特性进行了研究。单独使用时,该染料使细胞核、细胞质和胶原呈现红色。该染料可被弱碱提取,但不能被酸提取。染色性需要组织中的离子化氨基,并且也有证据表明该染料存在非离子结合。用铬变青R和氯化铁混合物染色所获得的颜色随铁与染料的摩尔比以及pH值而变化。仅在pH 1至2之间能看到有用的染色效果。组织要么全部染成蓝色(当铁与染料比例高时),要么同时染成红色和蓝色(当铁与染料比例低时)。较低的pH值有利于红色的沉积,较高的pH值有利于蓝色的沉积。红色主要存在于细胞质中,蓝色存在于细胞核和髓鞘中。胶原纤维呈红色或紫色,这取决于pH值和铁与染料的比例。红色可被酸分化,并通过弱碱变为蓝色,但不会被提取。染色切片中的红色物质显然不是游离染料,所以它可能是一种铁 - 染料复合物。从各种分化剂的作用可以推断,红色和蓝色染料 - 金属复合物分子是通过染料部分与组织结合的,而不是通过铁原子的插入。铁(III)与铬变青R的复合物染色不涉及核酸或其他聚阴离子或蛋白质的氨基。有证据表明红色和蓝色复合物都仅存在非离子结合。有人提出,用低铁与染料比例的溶液染色的切片中的红色是由于一种简单的羧酸盐复合物[Fe₂H(染料)]⁻。然后蓝色将由红色复合物失去一个质子生成[Fe₂(染料)]²⁻而产生。去除质子的碱可能是细胞核中富含精氨酸的核蛋白和髓鞘的磷脂碱。描述了用于两种颜色的信息性同时染色以及用于细胞核或髓鞘选择性染色的技术。