Kawamoto T, Shimizu M
Department of Biochemistry, School of Dental Medicine, Tsurumi University, Yokohama, Japan.
Histochem Cell Biol. 2000 May;113(5):331-9. doi: 10.1007/s004180000149.
This article describes a method for preparing 2- to 50-micron-thick fresh-frozen sections from large samples and completely calcified tissue samples. In order to perform the more routine work involved, a tungsten carbide disposable blade was installed to a heavy-duty sledge cryomicrotome. An entire 10-day-old rat and bone and tooth samples from a 7-month-old rat were rapidly frozen. The frozen samples were attached to the cryomicrotome stage. The cutting surface of the samples was covered with a polyvinylidene chloride film coated with synthetic rubber cement and cut at -25 degrees C. The soft tissues and the hard tissues were satisfactorily preserved and all tissue cells were easily identifiable. Enzymatic activity in the fresh sections was much stronger than that in chemically fixed and/or decalcified sections. The sections permitted histological and histochemical studies without trouble. In addition, the sections can be used for multiple experiments such as immunohistochemistry, in situ hybridization, and electron microprobe X-ray micro-analysis. This method can be used with conventional cryomicrotome equipment.
本文介绍了一种从大样本和完全钙化的组织样本制备2至50微米厚新鲜冷冻切片的方法。为了进行相关的常规工作,将一个碳化钨一次性刀片安装到一台重型雪橇式冷冻切片机上。将一只10日龄的大鼠整体以及一只7月龄大鼠的骨骼和牙齿样本迅速冷冻。将冷冻后的样本固定在冷冻切片机的载物台上。样本的切割面覆盖一层涂有合成橡胶胶水的聚偏二氯乙烯薄膜,并在-25℃下进行切割。软组织和硬组织均得到了良好保存,所有组织细胞都易于识别。新鲜切片中的酶活性比化学固定和/或脱钙切片中的要强得多。这些切片可顺利用于组织学和组织化学研究。此外,这些切片可用于多种实验,如免疫组织化学、原位杂交和电子探针X射线微分析。该方法可与传统的冷冻切片机设备配合使用。