Division of Infection and Immunity, Faculty of Biomedical and Life Sciences, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow G12 8TA, UK.
Parasitology. 2010 Jun;137(7):1089-98. doi: 10.1017/S0031182009991983. Epub 2010 Feb 4.
It has been observed that fluorescent membrane-impermeant molecules can enter the cercariae as they penetrate mouse skin. The hypothesis to be tested was that such molecules, which included Lucifer Yellow and a variety of fluorescent dextrans, entered the parasite through the nephridiopore and excretory tubules as well as through the surface membrane. FITC-labelled poly-L-lysine (molecular weight 10 kDa), added at 4 degrees C during syringe transformation, was found to enter the nephridiopore and labelled the excretory bladder and sometimes the excretory tubules. This finding indicates that macromolecules (10 kDa) can enter the nephridiopore. It was found that linoleic acid (a normal constituent of skin) greatly stimulated uptake of Lucifer Yellow and dextrans into the excretory/subtegumental region of 2-h-old schistosomula. This correlated with an increased uptake of membrane-impermeant propidium iodide at 37 degrees C. Since increased uptake of propidium iodide occurs when membranes become permeable, the surface membrane could also be a pathway of transport of the membrane-impermeant molecules into the schistosomulum.
已经观察到,荧光膜不可渗透的分子可以在尾蚴穿透小鼠皮肤时进入其中。待检验的假设是,这些分子(包括 Lucifer Yellow 和各种荧光葡聚糖)通过肾孔和排泄管以及表面膜进入寄生虫。在注射器转化过程中于 4°C 时添加的 FITC 标记的聚赖氨酸(分子量 10 kDa)被发现进入肾孔,并标记排泄囊,有时还标记排泄管。这一发现表明,大分子(10 kDa)可以进入肾孔。还发现亚油酸(皮肤的正常成分)极大地刺激 Lucifer Yellow 和葡聚糖进入 2 小时龄的尾蚴的排泄/表皮下区域的摄取。这与 37°C 时膜不可渗透的碘化丙啶摄取增加相关。由于膜通透性增加时碘化丙啶的摄取增加,因此表面膜也可能是膜不可渗透分子进入尾蚴的运输途径。