Derkx P, Birkenhäger-Frenkel D H
Department of Pathology, Erasmus University, Rotterdam, The Netherlands.
Biotech Histochem. 1995 Mar;70(2):70-4. doi: 10.3109/10520299509108320.
A staining method is described using thionin, for undecalcified deacrylated bone sections. RNA is stained purplish violet, allowing still active osteoblasts to be distinguished from lining cells. Staining intensity of mineralized bone is related to the degree of mineralization. Mineralizing fronts and cement lines are visualized clearly. Lamellae show an alternate pattern. Histomorphometric parameters such as osteon thickness and interstitial bone thickness can be measured without using polarized light. The mineralizing front can be assessed and expressed as a percentage of the osteoblast-covered interface between osteoid and mineralized bone. The stain is also useful for qualitative assessment of metabolic bone disease. Thionin stained sections can be kept for at least one year when stored in the dark at 7 C.
本文描述了一种使用硫堇对未脱钙、去丙烯酸化骨切片进行染色的方法。RNA被染成紫丁香色,从而能够区分仍具有活性的成骨细胞和衬里细胞。矿化骨的染色强度与矿化程度相关。矿化前沿和黏合线清晰可见。骨板呈现交替模式。无需使用偏振光即可测量诸如骨单位厚度和骨间质厚度等组织形态计量学参数。可以评估矿化前沿,并将其表示为类骨质与矿化骨之间成骨细胞覆盖界面的百分比。该染色方法对于代谢性骨病的定性评估也很有用。硫堇染色的切片在7℃黑暗条件下保存时可保存至少一年。