Hatae T, Fujita M, Okuyama K
Department of Anatomy, Kagawa Medical School, Japan.
Cell Tissue Res. 1988 Mar;251(3):511-21. doi: 10.1007/BF00213998.
The ileal absorptive cells of suckling rats exhibit high levels of endocytic activity being engaged in nonselective uptake of macromolecules from the intestinal lumen. The apical cytoplasm usually contains an extensive network of small, membrane-limited tubules (apical tubules: AT), in addition to newly formed endocytic vesicles and large endocytic vacuoles. To determine whether the AT are directly involved in the endocytic process by carrying the tracer into the cell, we have analysed movements of the apical cell membrane of the ileal absorptive cells by using a membrane-bound tracer (horseradish peroxidase-labelled concanavalin-A: Con-A HRP). The ileal absorptive cells were exposed in vitro to Con-A HRP for 10 min at 4 degrees C, incubated for different times in Con-A free medium at 37 degrees C, and prepared for electron microscopy. After 1 min incubation at 37 degrees C, invaginations of the apical cell membrane, including coated pits, and endocytic vesicles were labelled with HRP-reaction product, whereas the AT and large endocytic vacuoles were negative. After 2.5 min, almost all the large endocytic vacuoles were labelled with reaction product, which was seen in their vacuolar lumen and along the luminal surface of their limiting membrane. A few AT with reaction product were seen in the apical cytoplasm; they were in frequent connection with the reaction-positive large endocytic vacuoles. With increasing incubation time, the number of the labelled AT increased. Thus, after 15 min at 37 degrees C, the apical cytoplasm was fully occupied by the reaction-positive AT. The ends of these AT were often continuous with small spherical coated vesicles. No reaction product was detected in the Golgi complex at any time after incubation. These observations indicate that the AT located in the apical cytoplasm probably originate by budding off from the large endocytic vacuoles, rather than being involved in the process of endocytosis.
哺乳大鼠的回肠吸收细胞表现出高水平的内吞活性,参与从肠腔中非选择性摄取大分子。顶端细胞质通常除了新形成的内吞小泡和大的内吞液泡外,还含有广泛的小的、膜包被的小管网络(顶端小管:AT)。为了确定AT是否通过将示踪剂带入细胞而直接参与内吞过程,我们使用膜结合示踪剂(辣根过氧化物酶标记的伴刀豆球蛋白A:Con-A HRP)分析了回肠吸收细胞顶端细胞膜的运动。将回肠吸收细胞在体外于4℃下暴露于Con-A HRP 10分钟,然后在37℃下于无Con-A的培养基中孵育不同时间,并制备用于电子显微镜检查。在37℃孵育1分钟后,顶端细胞膜的内陷,包括被膜小窝和内吞小泡,被HRP反应产物标记,而AT和大的内吞液泡为阴性。2.5分钟后,几乎所有大的内吞液泡都被反应产物标记,反应产物见于其液泡腔和限制膜的腔面。在顶端细胞质中可见一些带有反应产物的AT;它们与反应阳性的大的内吞液泡频繁相连。随着孵育时间的增加,标记的AT数量增加。因此,在37℃孵育15分钟后,顶端细胞质完全被反应阳性的AT占据。这些AT的末端常常与小的球形被膜小泡连续。孵育后任何时候在高尔基体复合体中均未检测到反应产物。这些观察结果表明,位于顶端细胞质中的AT可能起源于从大的内吞液泡上出芽,而不是参与内吞过程。