Tada Masahito, Shinohara Yoshinori, Kato Ichiro, Hiraga Koichi, Aizawa Tomoyasu, Demura Makoto, Mori Yoshihiro, Shinoda Hiroyuki, Mizuguchi Mineyuki, Kawano Keiichi
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Toyama 930-0194, Japan.
Acta Histochem Cytochem. 2006 Apr 22;39(2):31-4. doi: 10.1267/ahc.05051. Epub 2006 Mar 29.
Hard tissue decalcification can cause variation in the constituent protein characteristics. This paper describes a method of preparating of frozen mouse head sections so as to clearly observe the nature of the constituent proteins. Frozen sections of various green fluorescent protein (GFP) transgenic mouse heads were prepared using the film method developed by Kawamoto and Shimizu. This method made specimen dissection without decalcification possible, wherein GFP was clearly observed in an undamaged state. Conversely, using the same method with decalcification made GFP observation in the transgenic mouse head difficult. This new method is suitable for observing GFP marked cells, enabling us to follow the transplanted GFP marked cells within frozen head sections.
硬组织脱钙会导致组成蛋白特性发生变化。本文描述了一种制备冷冻小鼠头部切片的方法,以便清晰观察组成蛋白的性质。使用河本和清水开发的薄膜法制备了各种绿色荧光蛋白(GFP)转基因小鼠头部的冷冻切片。这种方法使得在不脱钙的情况下进行标本解剖成为可能,其中绿色荧光蛋白在未受损状态下清晰可见。相反,在脱钙情况下使用相同方法会使转基因小鼠头部的绿色荧光蛋白观察变得困难。这种新方法适用于观察绿色荧光蛋白标记的细胞,使我们能够在冷冻头部切片中追踪移植的绿色荧光蛋白标记细胞。