Allen R D, Schroeder C C, Fok A K
Pacific Biomedical Research Center, University of Hawaii, Honolulu 96822.
J Cell Sci. 1992 Feb;101 ( Pt 2):449-61. doi: 10.1242/jcs.101.2.449.
A detailed morphological and tracer study of endocytosis via coated pits in Paramecium multimicronucleatum was undertaken to compare endocytic processes in a free-living protozoon with similar processes in higher organisms. Permanent pits at the cell surface enlarge, become coated and give rise to coated vesicles (188 +/- 41 nm in diameter) that enclose fluid-phase markers such as horseradish peroxidase (HRP). Both the pits and vesicles are labeled by the immunogold technique when a monoclonal antibody (mAb) raised against the plasma membrane of this cell is applied to cryosections. The HRP is delivered to an early endosome compartment, which also shares the plasma membrane antigen. The early endosome, as shown in quick-freeze deep-etch replicas of chemically unfixed cells, is a definitive non-reticular compartment composed of many individual flattened cisternal units of 0.2 to 0.7 microns diameter, each potentially bearing one or more approximately 80-nm-wide coated evaginations. These coated evaginations on the early endosomes contain HRP but are not labeled by the mAb. The coated evaginations pinch off to form a second group of coated vesicles (90 +/- 17 nm in diameter), which can be differentiated from those formed from coated pits by their smaller size, absence of plasma membrane antigen and their location somewhat deeper into the cytoplasm. This study shows a striking similarity between protozoons and mammalian cells in their overall early endosomal machinery and in the ability of early endosomes to sort cargo from plasma membrane components. The vesicles identified in this study form two distinct populations of putative shuttle vesicles, pre-endosomal (large) and early endosome-derived vesicles (small), which facilitate incoming and outgoing traffic from the early endosomes.
对多核草履虫中通过被膜小窝进行的内吞作用进行了详细的形态学和示踪研究,以比较自由生活的原生动物中的内吞过程与高等生物中的类似过程。细胞表面的永久性小窝会扩大,被包被并产生被膜小泡(直径188±41纳米),这些小泡包裹诸如辣根过氧化物酶(HRP)等液相标记物。当将针对该细胞的质膜产生的单克隆抗体(mAb)应用于冷冻切片时,小窝和小泡都通过免疫金技术进行标记。HRP被递送至早期内体区室,该区域也共享质膜抗原。如化学未固定细胞的快速冷冻深度蚀刻复制品所示,早期内体是一个明确的非网状区室,由许多直径为0.2至0.7微米的单个扁平囊状单元组成,每个单元可能带有一个或多个约80纳米宽的被膜出芽。早期内体上的这些被膜出芽含有HRP,但未被mAb标记。被膜出芽 pinched off形成第二组被膜小泡(直径90±17纳米),它们可以通过较小的尺寸、缺乏质膜抗原以及它们在细胞质中更深的位置与由被膜小窝形成的小泡区分开来。这项研究表明,原生动物和哺乳动物细胞在其整体早期内体机制以及早期内体从质膜成分中分拣货物的能力方面存在惊人的相似性。本研究中鉴定出的小泡形成了两个不同的假定穿梭小泡群体,即内体前(大)小泡和早期内体衍生小泡(小),它们促进了早期内体的进出运输。