Kacena M A, Troiano N W, Coady C E, Horowitz M C
Department of Orthopaedics and Rehabilitation, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Biotech Histochem. 2004 Oct-Dec;79(5-6):185-90. doi: 10.1080/10520290400015506.
We compared histochemical and immunohistochemical staining as well as fluorochrome labeling in murine bone specimens that were fixed with 10% neutral buffered formalin to those fixed with HistoChoice. We showed that sections from undecalcified tibiae fixed for 4 h in HistoChoice resulted in enhanced toluidine blue and Von Kossa histochemical staining compared to formalin fixation. HistoChoice produced comparable or improved staining for alkaline phosphatase. Acid phosphatase localization was better in formalin fixed specimens, but osteoclasts were visualized more easily in HistoChoice fixed specimens. As expected, immunohistochemical labeling was antibody dependent; some antibodies labeled better in HistoChoice fixed specimens while others were better in formalin fixed specimens. Toluidine blue, Von Kossa, and alkaline phosphatase staining of sections fixed for 12 h produced sections that were similar to 4 h fixed sections. Fixation for 12 h preserved acid phosphatase activity better. Increasing fixation to 12 h affected immunolocalization differentially. Bone sialoprotein labeling in HistoChoice fixed specimens was comparable to formalin fixed samples. On the other hand, after 12 h formalin fixation, osteocalcin labeling was comparable to HistoChoice. For most histochemical applications, fixing murine bone specimens for 4 h with HistoChoice yielded superior staining compared to formalin fixation. If immunohistochemical localization is desired, however, individual antibodies must be tested to determine which fixation process retains antigenicity better. In addition, there was no detectable difference in the intensity of fluorochrome labeling using either fixative. Finally, fixation duration did not alter the intensity of labeling.
我们比较了用10%中性缓冲福尔马林固定的小鼠骨标本与用HistoChoice固定的标本的组织化学和免疫组织化学染色以及荧光染料标记。我们发现,与福尔马林固定相比,在HistoChoice中固定4小时的未脱钙胫骨切片,甲苯胺蓝和冯·科萨组织化学染色增强。HistoChoice对碱性磷酸酶产生了相当或更好的染色效果。酸性磷酸酶在福尔马林固定的标本中定位更好,但在HistoChoice固定的标本中破骨细胞更容易可视化。正如预期的那样,免疫组织化学标记依赖于抗体;一些抗体在HistoChoice固定的标本中标记效果更好,而另一些在福尔马林固定的标本中更好。固定12小时的切片的甲苯胺蓝、冯·科萨和碱性磷酸酶染色产生的切片与固定4小时的切片相似。固定12小时能更好地保留酸性磷酸酶活性。将固定时间增加到12小时对免疫定位有不同的影响。HistoChoice固定标本中的骨唾液蛋白标记与福尔马林固定样本相当。另一方面,福尔马林固定12小时后,骨钙素标记与HistoChoice相当。对于大多数组织化学应用,与福尔马林固定相比,用HistoChoice固定小鼠骨标本4小时能产生更好的染色效果。然而,如果需要免疫组织化学定位,则必须测试个别抗体以确定哪种固定方法能更好地保留抗原性。此外,使用任何一种固定剂的荧光染料标记强度均无可检测到的差异。最后,固定持续时间并未改变标记强度。