Shepard N, Mitchell N
Histochemistry. 1981;70(2):107-14. doi: 10.1007/BF00493202.
This study indicated that acridine orange, when combined with the initial fixative stabilized soluble matrix glycosaminoglycan in situ in areas where considerable glycosaminoglycan extraction is known to occur. Acridine orange was able to diffuse through bone into areas of undecalcified mineralizing cartilage and to bind with the glycosaminoglycans in these areas equally well as in growth plate cartilage matrix. Matrix staining was visible by light microscopy without further staining and was seen to vary territorially in intensity; although cellular definition was poor. This deficiency was overcome by the additional application of p phenylenediamine which stained the cells intensely. At the ultrastructure level, glycosaminoglycan was present as electron dense structures in the cartilage matrix. Preliminary X-ray microanalysis studies confirmed that the acridine orange stained structures contain sulphur; this finding extends the use of acridine orange further to quantitative analysis of glycosaminoglycan.
本研究表明,吖啶橙与初始固定剂联合使用时,能在已知会发生大量糖胺聚糖提取的区域原位稳定可溶性基质糖胺聚糖。吖啶橙能够扩散穿过骨骼进入未脱钙的矿化软骨区域,并与这些区域的糖胺聚糖结合,其效果与生长板软骨基质中的情况一样好。基质染色在光学显微镜下无需进一步染色即可看见,且在不同区域强度有所变化;尽管细胞清晰度较差。通过额外使用对苯二胺对细胞进行强烈染色,这一缺陷得以克服。在超微结构水平上,糖胺聚糖以电子致密结构存在于软骨基质中。初步的X射线微分析研究证实,吖啶橙染色的结构含有硫;这一发现进一步拓展了吖啶橙在糖胺聚糖定量分析方面的应用。