Miki A, Kugler P
Histochemistry. 1986;85(2):169-75. doi: 10.1007/BF00491765.
The effect of exposure to leupeptin (25 micrograms/ml for 24 h) on the endocytotic activity and the membrane flow of apical cell membranes was studied in endodermal cells of cultured rat visceral yolk sacs by applying a double-labelling method using concanavalin-A ferritin (Con-A Fer) and horseradish peroxidase (HRP). Control and leupeptin-treated yolk sacs were labelled with Con-A Fer at 4 degrees C and then incubated with HRP for 5, 15 or 60 min at 37 degrees C. In controls, HRP reaction product was detected after 5 min in many of the apical vacuoles as well as a few lysosomes; after 15 min, reaction product was observed in all apical vacuoles and in lysosomes of various sizes. These HRP-positive structures usually contained a variable amount of membrane-bound Fer. After 60 min, all apical vacuoles and almost all lysosomes exhibited HRP reactions, but only some of these structures contained Fer particles. At this time, many apical canaliculi (which are involved in membrane recycling) exhibited positive HRP reactions and sometimes also contained Fer particles. In leupeptin-treated cells, HRP reaction product and variable amounts of membrane-bound Fer particles were found in apical vacuoles after 5 min; after 15 min, both labels were also observed in some small lysosomes, and after 60 min, they were found in all apical vacuoles as well as some small and middle-sized lysosomes. Significantly fewer labelled apical vacuoles, lysosomes and apical canaliculi were present after leupeptin treatment than in controls at corresponding times. At all times examined, the giant lysosomes found in leupeptin-treated cells did not exhibit any labeling.(ABSTRACT TRUNCATED AT 250 WORDS)
通过使用伴刀豆球蛋白A铁蛋白(Con - A Fer)和辣根过氧化物酶(HRP)的双重标记方法,研究了在培养的大鼠内脏卵黄囊内胚层细胞中,暴露于亮抑酶肽(25微克/毫升,持续24小时)对顶端细胞膜的内吞活性和膜流动的影响。对照和经亮抑酶肽处理的卵黄囊在4℃用Con - A Fer标记,然后在37℃与HRP孵育5、15或60分钟。在对照中,5分钟后在许多顶端液泡以及一些溶酶体中检测到HRP反应产物;15分钟后,在所有顶端液泡和各种大小的溶酶体中观察到反应产物。这些HRP阳性结构通常含有不同量的膜结合铁蛋白。60分钟后,所有顶端液泡和几乎所有溶酶体都表现出HRP反应,但只有一些这些结构含有铁蛋白颗粒。此时,许多参与膜回收的顶端小管表现出阳性HRP反应,有时也含有铁蛋白颗粒。在经亮抑酶肽处理的细胞中,5分钟后在顶端液泡中发现HRP反应产物和不同量的膜结合铁蛋白颗粒;15分钟后,在一些小溶酶体中也观察到这两种标记,60分钟后,在所有顶端液泡以及一些中小溶酶体中发现它们。与相应时间的对照相比,亮抑酶肽处理后标记的顶端液泡、溶酶体和顶端小管明显减少。在所有检查时间,在经亮抑酶肽处理的细胞中发现的巨大溶酶体未表现出任何标记。(摘要截短于250字)