Suzuki S, Furihata C, Tsuyama S, Murata F
Histochemistry. 1983;79(2):167-76. doi: 10.1007/BF00489779.
The localization of pepsinogen in rat stomachs was investigated by a postembedding immunoferritin method. When the preparations embedded in Epon were used, the secretory granules of chief cells were stained heavily and the granules of mucous neck cells were stained moderately. The secretory granules of cells intermediate between mucous neck cells and chief cells showed a bizonal staining; the electron dense parts were stained heavily and the electron lucent parts were stained moderately. The secretory granules of pyloric gland cells, on the other hand, were labeled faintly. However, the secretory granules of surface mucous cells, foveolar mucous cells, endocrine cells, cardiac mucous cells and cardiac serous cells were not stained by the method. The protein A-gold method showed a similar staining pattern of pepsinogen to that of the immunoferritin method. When the samples embedded in Lowicryl K4M were used to enhance the stainability of pepsinogen, essentially the same staining pattern as that of the samples embedded in Epon was obtained. In addition, the Golgi apparatus and the rough surfaced endoplasmic reticulum were more easily stained.
采用包埋后免疫铁蛋白法研究了大鼠胃中胃蛋白酶原的定位。当使用包埋在环氧树脂中的标本时,主细胞的分泌颗粒被重度染色,黏液颈细胞的颗粒被中度染色。黏液颈细胞和主细胞之间的中间细胞的分泌颗粒呈现双区染色;电子致密部分被重度染色,电子透亮部分被中度染色。另一方面,幽门腺细胞的分泌颗粒被微弱标记。然而,表面黏液细胞、小凹黏液细胞、内分泌细胞、贲门黏液细胞和贲门浆液细胞的分泌颗粒未被该方法染色。蛋白A-金法显示胃蛋白酶原的染色模式与免疫铁蛋白法相似。当使用包埋在Lowicryl K4M中的样品来增强胃蛋白酶原的染色性时,获得了与包埋在环氧树脂中的样品基本相同的染色模式。此外,高尔基体和粗面内质网更容易被染色。