Friedrich K, Seiffert W, Zimmermann H W
Institut für Physikalische Chemie, Universität Freiburg, Federal Republic of Germany.
Histochemistry. 1990;93(3):247-56. doi: 10.1007/BF00266385.
A reproducible Romanowsky-Giemsa staining (RGS) can be carried out with standardized staining solutions containing the two dyes azure B (AB) and eosin Y (EY). After staining, cell nuclei have a purple coloration generated by DNA-AB-EY complexes. The microspectra of cell nuclei have a sharp and intense absorption band at 18,100 cm-1 (552 nm), the so called Romanowsky band (RB), which is due to the EY chromophore of the dye complexes. Other absorption bands can be assigned to the DNA-bound AB cations. Artificial DNA-AB-EY complexes can be prepared outside the cell by subsequent staining of DNA with AB and EY. In the first step of our staining experiments we prepared thin films of blue DNA-AB complexes on microslides with 1:1 composition: each anionic phosphodiester residue of the nucleic acid was occupied by one AB cation. Microspectrophotometric investigations of the dye preparations demonstrated that, besides monomers and dimers, mainly higher AB aggregates are bound to DNA by electrostatic and hydrophobic interactions. These DNA-AB complexes are insoluble in water. Therefore it was possible to stain the DNA-AB films with aqueous EY solutions and also to prepare insoluble DNA-AB-EY films in the second step of the staining experiments. After the reaction with EY, thin sites within the dye preparations were purple. The microspectra of the purple spots show a strong Romanowsky band at 18,100 cm-1. Using a special technique it was possible to estimate the composition of the purple dye complexes. The ratio of the two dyes was approximately EY:AB approximately 1:3. The EY anions are mainly bound by hydrophobic interaction to the AB framework of the electrical neutral DNA-AB complexes. The EY absorption is red shifted by the interaction of EY with the AB framework of DNA-AB-EY. We suppose that this red shift is caused by a dielectric polarization of the bound EY dianions. The DNA chains in the DNA-AB complexes can mechanically be aligned in a preferred direction k. Highly oriented dye complexes prepared on microslides were birefringent and dichroic. The orientation is maintained during subsequent staining with aqueous EY solutions. In this way we also prepared highly orientated purple DNA-AB-EY complexes on microslides. The light absorption of both types of dye complexes was studied by means of a microspectrophotometer equipped with a polarizer and an analyser. The sites of best orientation within the dye preparations were selected under crossed nicols according to the quality of birefringence.(ABSTRACT TRUNCATED AT 400 WORDS)
使用含有天青B(AB)和伊红Y(EY)这两种染料的标准化染色溶液,可进行可重复的罗曼诺夫斯基 - 吉姆萨染色(RGS)。染色后,细胞核因DNA - AB - EY复合物而呈现紫色。细胞核的微观光谱在18,100 cm⁻¹(552 nm)处有一个尖锐且强烈的吸收带,即所谓的罗曼诺夫斯基带(RB),这是由于染料复合物中的EY发色团所致。其他吸收带可归因于与DNA结合的AB阳离子。通过用AB和EY对DNA进行后续染色,可在细胞外制备人工DNA - AB - EY复合物。在我们染色实验的第一步中,我们在载玻片上制备了1:1组成的蓝色DNA - AB复合物薄膜:核酸的每个阴离子磷酸二酯残基被一个AB阳离子占据。对染料制剂的微观分光光度研究表明,除了单体和二聚体之外,主要是更高的AB聚集体通过静电和疏水相互作用与DNA结合。这些DNA - AB复合物不溶于水。因此,在染色实验的第二步中,可用EY水溶液对DNA - AB薄膜进行染色,也可制备不溶性的DNA - AB - EY薄膜。与EY反应后,染料制剂中的薄区域呈紫色。紫色斑点的微观光谱在18,100 cm⁻¹处显示出强烈的罗曼诺夫斯基带。使用一种特殊技术可以估计紫色染料复合物的组成。两种染料的比例约为EY:AB约为1:3。EY阴离子主要通过疏水相互作用与电中性DNA - AB复合物的AB框架结合。EY的吸收由于EY与DNA - AB - EY的AB框架相互作用而发生红移。我们推测这种红移是由结合的EY二价阴离子中的介电极化引起的。DNA - AB复合物中的DNA链可以在一个优选方向k上机械排列。在载玻片上制备的高度取向的染料复合物具有双折射和二向色性。在用EY水溶液进行后续染色过程中,这种取向得以保持。通过这种方式,我们还在载玻片上制备了高度取向的紫色DNA - AB - EY复合物。使用配备有起偏器和检偏器的微观分光光度计研究了这两种染料复合物的光吸收。根据双折射质量,在正交尼科尔棱镜下选择染料制剂中取向最佳的区域。(摘要截取自400字)