Hansen G H, Sjöström H, Norén O, Dabelsteen E
Eur J Cell Biol. 1987 Apr;43(2):253-9.
The subcellular localization of aminopeptidase N (EC 3.4.11.2) in the pig enterocyte was investigated by immunofluorescence and immunoelectron microscopy (immunogold staining). By indirect immunofluorescence on either frozen or paraffin-embedded sections, a very intense staining in the microvillar membrane and a weak intracellular staining was demonstrated. No staining was detected in the basolateral membrane. Likewise, the immunogold labelling on Epon-embedded sections was concentrated in the microvillar membrane, whereas the basolateral membrane did not contain significant amounts of labelling. Labelling was demonstrated in the Golgi apparatus and in a minor fraction of the intracellular smooth vesicles positioned between the Golgi apparatus and the microvillar membrane. These observations are compatible with the view that newly synthesized aminopeptidase N is delivered directly to the microvillar membrane by smooth vesicles having a diameter about 70 to 100 nm and does not pass the basolateral membrane on its way to the brush border membrane.
通过免疫荧光和免疫电子显微镜(免疫金染色)研究了猪肠上皮细胞中氨肽酶N(EC 3.4.11.2)的亚细胞定位。在冷冻切片或石蜡包埋切片上进行间接免疫荧光检测时,微绒毛膜呈现非常强烈的染色,而细胞内染色较弱。在基底外侧膜未检测到染色。同样,在环氧树脂包埋切片上的免疫金标记集中在微绒毛膜上,而基底外侧膜没有大量标记。在高尔基体以及位于高尔基体和微绒毛膜之间的一小部分细胞内光滑囊泡中也显示有标记。这些观察结果与以下观点相符,即新合成的氨肽酶N由直径约70至100nm的光滑囊泡直接输送到微绒毛膜,并且在其到达刷状缘膜的途中不经过基底外侧膜。