Cooper M D, McGraw P A, Melly M A
Infect Immun. 1986 Feb;51(2):425-30. doi: 10.1128/iai.51.2.425-430.1986.
An experimental model using human fallopian tubes in organ culture was used to study the localization of purified gonococcal lipopolysaccharide (LPS). LPS was visualized by light microscopy with immunoperoxidase staining. Immediately after addition to fallopian tube organ cultures, gonococcal LPS aggregated on the tips of cilia. By 1 to 2 h after exposure, LPS could be seen distributed throughout the cytoplasm of ciliated and nonciliated cells in structures resembling vesicles. By 12 h, there were sloughed, ciliated cells present in the fallopian tube lumen, which had positive LPS stain on their surfaces as well as in their cytoplasm. By 24 h, LPS was distributed throughout the cytoplasm. Control experiments with rabbit oviduct organ cultures showed that LPS failed to attach, enter, or damage mucosal cells. These studies illustrate the initial localization of LPS on human mucosal cells and its uptake into the cells, which are coincident with toxicity for ciliated epithelial cells.
利用人体输卵管器官培养的实验模型来研究纯化的淋球菌脂多糖(LPS)的定位。通过免疫过氧化物酶染色,利用光学显微镜观察LPS。将其添加到输卵管器官培养物后,淋球菌LPS立即聚集在纤毛尖端。暴露1至2小时后,可看到LPS分布在类似小泡结构的纤毛细胞和非纤毛细胞的整个细胞质中。到12小时时,输卵管腔中有脱落的纤毛细胞,其表面和细胞质中LPS染色呈阳性。到24小时时,LPS分布在整个细胞质中。对兔输卵管器官培养的对照实验表明,LPS无法附着、进入或损伤黏膜细胞。这些研究阐明了LPS在人体黏膜细胞上的初始定位及其被细胞摄取的过程,这与对纤毛上皮细胞的毒性是一致的。