Punnonen E L, Marjomäki V S, Reunanen H
Department of Cell Biology, University of Jyväskylä, Finland.
Eur J Cell Biol. 1994 Oct;65(1):14-25.
The effect of 3-methyladenine on transport from endosomes to lysosomes was studied in rat embryonic and mouse 3T3 fibroblasts. Subcellular fractionation in 27% Percoll gradients showed that the pre-endocytosed (5 min pulse) horseradish peroxidase (HRP) was not transported from endosomes to dense lysosomes in cells chased in the presence of 10 mM 3-methyladenine. However, fractionation in 20% Percoll gradients, which separated early endosomes from late endosomes and lysosomes, as well as light and electron microscopic experiments, showed that HRP was transported from early endosomes to the perinuclear late endosomes. Immunoprecipitation of metabolically labeled cells was used to study the biosynthetic processing of a lysosomal proteinase, cathepsin L. The results showed that the early processing of the precursor to the intermediate form was not affected by 3-methyladenine, while the late processing of the intermediate to the mature form was retarded. In addition, immunofluorescence labeling showed that 3-methyladenine treatment caused accumulation of cathepsin L in the perinuclear area. Another lysosomal enzyme, beta-glucuronidase, was normally distributed in both perinuclear and peripheral vesicles which indicated that the localization of lysosomes was not altered. The results thus suggest that the late processing of cathepsin L was inhibited because transport from perinuclear endosomes to lysosomes was retarded. In conclusion, both endocytic pulse-chase experiments and immunoprecipitation of metabolically labeled cathepsin L indicate that 3-methyladenine inhibits transport from late endosomes to mature lysosomes in both rat and mouse fibroblasts.
在大鼠胚胎成纤维细胞和小鼠3T3成纤维细胞中研究了3-甲基腺嘌呤对从内体到溶酶体转运的影响。在27% Percoll梯度中进行亚细胞分级分离显示,在10 mM 3-甲基腺嘌呤存在下进行追踪的细胞中,预先内吞(5分钟脉冲)的辣根过氧化物酶(HRP)没有从内体转运到致密溶酶体。然而,在20% Percoll梯度中进行分级分离,该梯度可将早期内体与晚期内体和溶酶体分离,以及光镜和电镜实验表明,HRP从早期内体转运到核周晚期内体。利用代谢标记细胞的免疫沉淀法研究溶酶体蛋白酶组织蛋白酶L的生物合成加工过程。结果表明,前体向中间形式的早期加工不受3-甲基腺嘌呤的影响,而中间形式向成熟形式的晚期加工则受到阻碍。此外,免疫荧光标记显示,3-甲基腺嘌呤处理导致组织蛋白酶L在核周区域积累。另一种溶酶体酶β-葡萄糖醛酸酶正常分布在核周和外周小泡中,这表明溶酶体的定位没有改变。因此,结果表明组织蛋白酶L的晚期加工受到抑制是因为从核周内体到溶酶体的转运受到阻碍。总之,内吞脉冲追踪实验和代谢标记的组织蛋白酶L免疫沉淀均表明,3-甲基腺嘌呤抑制大鼠和小鼠成纤维细胞中从晚期内体到成熟溶酶体的转运。